pval,common_node,dm_node,disease,mshid,number_nodes,fdr
1.16E-303,160,204,Seborrheic dermatitis of scalp,D063807,4,7.75E-300
2.42E-299,158,201,SPINOCEREBELLAR ATAXIA 23,C537201,1,1.62E-295
2.42E-299,158,201,Sensation Disorders,D012678,1,1.62E-295
2.42E-299,158,201,Plague,D010930,1,1.62E-295
2.42E-299,158,201,Irritable Mood,D007508,1,1.62E-295
5.35E-298,160,213,Onychomycosis,D014009,15,3.58E-294
3.31E-296,157,201,Pentosuria,C536652,1,2.22E-292
3.31E-296,157,201,Bacteroides Infections,D001442,1,2.22E-292
1.73E-295,158,207,Cheilitis,D002613,10,1.16E-291
9.40E-294,159,215,Oral candidiasis,D002180,18,6.29E-290
2.28E-290,159,221,"Candidiasis, Chronic Mucocutaneous",D002178,23,1.52E-286
5.30E-290,155,201,Tyrosine Kinase 2 Deficiency,C566928,1,3.54E-286
5.30E-290,155,201,Leukoerythroblastic Anemia,D000750,1,3.54E-286
5.30E-290,155,201,"INFLAMMATORY BOWEL DISEASE 25, AUTOSOMAL RECESSIVE",C567251,1,3.54E-286
2.27E-289,155,202,COLD-INDUCED SWEATING SYNDROME 1,C536214,3,1.52E-285
2.27E-289,155,202,Bronchial Spasm,D001986,3,1.52E-285
3.98E-288,155,204,Intraabdominal Infections,D059413,4,2.66E-284
3.98E-288,155,204,STUVE-WIEDEMANN SYNDROME,C537502,4,2.66E-284
1.06E-287,157,215,Lobomycosis,D060368,16,7.06E-284
1.45E-287,156,210,"Hand, Foot and Mouth Disease",D006232,17,9.70E-284
6.21E-287,154,201,"Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant",C567925,1,4.15E-283
2.61E-286,154,202,"Rheumatoid Arthritis, Systemic Juvenile",C565798,3,1.74E-282
3.75E-284,156,216,Gastroenteritis,D005759,24,2.51E-280
6.94E-284,154,206,"Amyloidosis, Primary Cutaneous",C562642,7,4.63E-280
6.94E-284,154,206,Entamoeba histolytica Infection,D004749,6,4.63E-280
6.94E-284,153,201,"Glutaric aciduria, type 1",C536833,3,4.63E-280
2.08E-283,155,212,Genital Herpes,D006558,12,1.39E-279
6.94E-284,153,201,"Cardiac Output, High",D016534,1,4.63E-280
6.94E-284,153,201,Fetal Resorption,D005327,1,4.63E-280
6.94E-284,153,201,Galactorrhea not associated with childbirth,C537072,1,4.63E-280
6.94E-284,153,201,"Tuberculosis, Laryngeal",D014387,1,4.63E-280
6.94E-284,153,201,"Ventricular Dysfunction, Right",D018497,1,4.63E-280
6.94E-284,153,201,"Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, NK Cell-Negative",C563440,1,4.63E-280
6.94E-284,153,201,Infant Gynecomastia,D006177,1,4.63E-280
6.94E-284,153,201,Episodic Cluster Headache,D003027,1,4.63E-280
6.94E-284,153,201,Puerperal Disorders,D011644,1,4.63E-280
2.85E-283,153,202,"Severe Combined Immunodeficiency, Autosomal Recessive, T Cell Negative, B Cell Positive, NK Cell Positive",C563822,3,1.90E-279
2.85E-283,153,202,Evans syndrome,C536380,3,1.90E-279
2.85E-283,153,202,"Deafness, Sudden",D003639,3,1.90E-279
2.85E-283,153,202,Tinea,D014005,2,1.90E-279
2.85E-283,153,202,"Arthropathy, Erosive",C565273,2,1.90E-279
2.85E-283,153,202,Pestivirus Infections,D018182,2,1.90E-279
2.85E-283,153,202,Leukemoid Reaction,D007955,2,1.90E-279
2.85E-283,153,202,"Neutrophilia, Hereditary",C563010,2,1.90E-279
2.85E-283,153,202,"Mycobacterium Infections, Nontuberculous",D009165,2,1.90E-279
2.85E-283,153,202,Mikulicz Disease,D008882,2,1.90E-279
1.04E-282,154,208,Chills,D023341,10,6.91E-279
1.62E-282,156,219,Job Syndrome,D007589,21,1.08E-278
1.15E-282,153,203,Milk Allergy,D016269,3,7.68E-279
1.15E-282,153,203,Eyelid Diseases,D005141,3,7.68E-279
2.76E-282,155,214,Candidiasis of vagina,D002181,19,1.84E-278
4.60E-282,153,204,Thrombocytopenia-Absent Radius Syndrome,C536940,7,3.06E-278
4.60E-282,153,204,Schimke immunoosseous dysplasia,C536629,6,3.06E-278
4.60E-282,153,204,Fungemia,D016469,5,3.06E-278
4.60E-282,153,204,Scleritis,D015423,5,3.06E-278
4.60E-282,153,204,"Hepatitis D, Chronic",D019701,5,3.06E-278
4.60E-282,153,204,Rasmussen Syndrome,D004660,5,3.06E-278
4.60E-282,153,204,Bluetongue infection,D001819,4,3.06E-278
1.81E-281,153,205,Erythromelalgia,D004916,8,1.20E-277
1.81E-281,153,205,Acute-Phase Reaction,D000210,6,1.20E-277
1.81E-281,153,205,Chorioretinitis,D002825,5,1.20E-277
8.97E-281,157,228,X-Linked Combined Immunodeficiency Diseases,D053632,30,5.95E-277
7.02E-281,153,206,Venezuelan equine encephalomyelitis,D004685,9,4.66E-277
7.02E-281,153,206,"IgE RESPONSIVENESS, ATOPIC",C564133,8,4.66E-277
7.02E-281,153,206,Fatal Familial Insomnia,D034062,8,4.66E-277
2.68E-280,153,207,Cytomegalovirus Retinitis,D017726,7,1.78E-276
2.68E-280,153,207,Status Asthmaticus,D013224,7,1.78E-276
2.68E-280,153,207,"Bronchiolitis, Viral",D001990,7,1.78E-276
2.97E-280,152,202,Subacute Bacterial Endocarditis,D004698,6,1.97E-276
7.13E-280,154,213,"Colitis, Lymphocytic",D046730,14,4.73E-276
1.01E-279,153,208,Lambert-Eaton Myasthenic Syndrome,D015624,13,6.71E-276
1.18E-279,152,203,Rasmussen subacute encephalitis,C535291,4,7.82E-276
1.18E-279,152,203,"Paresthesia, Distal",D010292,4,7.82E-276
1.18E-279,152,203,Kimura Disease,D000796,3,7.82E-276
1.18E-279,152,203,Typhlitis,D053706,3,7.82E-276
4.62E-279,152,204,"Colitis, Microscopic",D046728,5,3.06E-275
1.61E-278,155,221,Rubella,D012409,29,1.07E-274
2.45E-278,158,239,Pneumococcal Infections,D011008,41,1.62E-274
1.78E-278,152,205,Erythema Infectiosum,D016731,7,1.18E-274
1.78E-278,152,205,Bilateral Headache,D006261,5,1.18E-274
1.78E-278,152,205,"Hemorrhagic Fever, Crimean",D006479,5,1.18E-274
1.78E-278,152,205,Secondary Peritonitis,D010538,5,1.18E-274
1.78E-278,152,205,Chemical Burns,D002057,5,1.18E-274
3.10E-278,154,216,"Colitis, Collagenous",D046729,16,2.05E-274
5.02E-278,153,211,Erythrocytosis,D011086,12,3.32E-274
5.02E-278,153,211,Immediate hypersensitivity,D006969,11,3.32E-274
6.77E-278,152,206,Juvenile pauciarticular chronic arthritis,C536312,7,4.48E-274
1.06E-277,154,217,Eczema Herpeticum,D007617,18,7.03E-274
1.74E-277,155,223,Oral Ulcer,D019226,26,1.15E-273
1.80E-277,153,212,Middle East Respiratory Syndrome,D018352,14,1.19E-273
1.80E-277,153,212,Helicobacter Infections,D016481,13,1.19E-273
7.49E-278,151,201,AIDS-Related Opportunistic Infections,D017088,1,4.95E-274
7.49E-278,151,201,Laron syndrome type 2,C537871,1,4.95E-274
7.49E-278,151,201,Wells syndrome,C536693,1,4.95E-274
2.54E-277,152,207,Polyomavirus Infections,D027601,7,1.68E-273
7.04E-277,156,230,"Eczema, Infantile",D003876,34,4.65E-273
2.96E-277,151,202,Ferrochelatase deficiency,D046351,3,1.95E-273
2.96E-277,151,202,"Chromosome 9, trisomy",C538028,2,1.95E-273
9.41E-277,152,208,"Multiple Sclerosis, Primary Progressive",D020528,11,6.21E-273
9.41E-277,152,208,Distemper,D004216,8,6.21E-273
1.15E-276,151,203,"Skin Diseases, Viral",D017193,3,7.60E-273
4.67E-276,160,257,Uveomeningoencephalitic Syndrome,D014607,63,3.08E-272
4.42E-276,151,204,Lassitude,D005221,4,2.92E-272
1.33E-275,154,221,"Malaria, Vivax",D016780,24,8.75E-272
1.24E-275,152,210,Foot-and-Mouth Disease,D005536,13,8.20E-272
1.24E-275,152,210,Folliculitis,D005499,12,8.20E-272
1.67E-275,151,205,Snoring,D012913,6,1.10E-271
4.43E-275,152,211,Hypoplastic anemia,D000741,13,2.92E-271
4.43E-275,152,211,Pure Red-Cell Aplasia,D012010,11,2.92E-271
8.89E-275,153,217,Hidradenitis Suppurativa,D017497,18,5.86E-271
8.89E-275,153,217,Angiolymphoid hyperplasia,D005871,17,5.86E-271
1.48E-274,157,241,Parasitic Diseases,D010272,47,9.75E-271
1.39E-274,154,223,Upper Respiratory Infections,D012141,28,9.17E-271
1.99E-274,162,275,Mycobacterium Infections,D009164,88,1.31E-270
1.56E-274,152,212,Filarial Elephantiases,D004605,16,1.03E-270
1.56E-274,152,212,Urticaria Pigmentosa,D014582,13,1.03E-270
2.97E-274,153,218,Erythema Nodosum,D004893,22,1.96E-270
7.25E-275,150,201,Proprotein Convertase 1 3 Deficiency,C563423,1,4.78E-271
9.84E-274,153,219,"Asthma, Aspirin-Induced",D055963,19,6.48E-270
8.37E-274,151,208,Laron Syndrome,D046150,8,5.51E-270
2.12E-273,158,250,Bronchiolitis,D001988,55,1.39E-269
1.07E-273,150,203,Klippel-Trenaunay-Weber Syndrome,D007715,4,7.06E-270
1.07E-273,150,203,Pediatric ulcerative colitis,C536315,3,7.06E-270
1.07E-273,150,203,Dysentery,D004403,3,7.06E-270
4.84E-273,155,232,Hepatitis D Infection,D003699,41,3.18E-269
4.39E-273,154,226,Hypergammaglobulinemia,D006942,28,2.89E-269
3.01E-273,151,209,"Thrombocytosis, Autosomal Dominant",D013920,9,1.98E-269
4.39E-273,154,226,Trachoma,D014141,26,2.89E-269
1.04E-272,153,221,Pulmonary Alveolar Proteinosis,D011649,30,6.86E-269
5.51E-272,150,206,Pycnodysostosis,D058631,6,3.62E-268
1.27E-271,154,229,Polyglandular Type I Autoimmune Syndrome,D016884,35,8.36E-268
6.71E-272,149,201,"Arthrogryposis multiplex congenita, distal type 2",C535379,1,4.41E-268
6.71E-272,149,201,"Insulin-Like Growth Factor I, Resistance to, due to Increased Binding Protein",C564817,1,4.41E-268
6.71E-272,149,201,Preeclamptic toxemia,C538543,1,4.41E-268
6.71E-272,149,201,"COLLAGENOSIS, FAMILIAL REACTIVE PERFORATING",C565687,1,4.41E-268
6.71E-272,149,201,Tinea Capitis,D014006,1,4.41E-268
6.71E-272,149,201,Aleutian Mink Disease,D000453,1,4.41E-268
6.71E-272,149,201,"Pyloric Stenosis, Infantile Hypertrophic, 5",C567283,1,4.41E-268
6.71E-272,149,201,"Surfactant Metabolism Dysfunction, Pulmonary, 1",C566882,1,4.41E-268
6.71E-272,149,201,"SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 2 (disorder)",C567048,1,4.41E-268
3.85E-271,154,230,"Pneumonia, Bacterial",D018410,31,2.52E-267
2.55E-271,149,202,Alveolar capillary dysplasia,C536590,5,1.67E-267
2.55E-271,149,202,Thyroid Dyshormonogenesis 5,C562771,3,1.67E-267
2.55E-271,149,202,RDS - infants,C538359,2,1.67E-267
2.55E-271,149,202,"Pulmonary alveolar proteinosis, congenital",C535832,2,1.67E-267
2.55E-271,149,202,Chilblains,D002647,2,1.67E-267
2.19E-270,156,244,Severe Dengue,D019595,55,1.44E-266
9.55E-271,149,203,Surfactant Dysfunction,C580477,3,6.26E-267
9.55E-271,149,203,Hypophysitis,D000072659,3,6.26E-267
9.55E-271,149,203,"Chromosome 22q11.2 Deletion Syndrome, Distal",C567511,3,6.26E-267
2.47E-270,152,220,Rheumatoid Nodule,D012218,20,1.62E-266
3.53E-270,149,204,Lennox-Gastaut syndrome,D065768,7,2.31E-266
3.53E-270,149,204,Congenital macrodactylia,C562546,6,2.31E-266
9.85E-270,153,227,Brucellosis,D002006,32,6.45E-266
8.78E-270,150,210,Hyaline Membrane Disease,D006819,11,5.75E-266
2.53E-269,157,253,Pustulosis of Palms and Soles,D011565,63,1.66E-265
4.65E-269,149,206,Desquamative interstitial pneumonia,C562470,6,3.04E-265
1.19E-268,156,248,Parasitemia,D018512,61,7.81E-265
1.78E-268,151,218,Yellow Fever,D015004,23,1.16E-264
2.42E-268,152,224,Complete trisomy 18 syndrome,D000073842,30,1.58E-264
5.93E-269,148,201,"Interferon gamma, receptor 1, deficiency",C535530,1,3.88E-265
4.42E-268,157,256,Mitral Valve Stenosis,D008946,68,2.89E-264
4.75E-268,159,270,"Leishmaniasis, Visceral",D007898,79,3.10E-264
3.48E-268,150,213,Pediatric Crohn's disease,C536215,15,2.28E-264
5.10E-268,155,243,Lymphocytic Choriomeningitis,D008216,50,3.33E-264
2.02E-267,149,209,Rales,D012135,13,1.32E-263
4.83E-267,160,280,"Cholangitis, Sclerosing",D015209,118,3.16E-263
5.71E-267,151,221,Familial erythrocytosis,C536842,23,3.73E-263
5.53E-266,153,235,Tropical Spastic Paraparesis,D015493,35,3.61E-262
3.75E-266,148,206,Miller-McKusick-Malvaux-Syndrome (3M Syndrome),C535314,8,2.45E-262
5.02E-266,147,201,Emaciation,D004614,2,3.28E-262
2.03E-265,159,277,"Periodontitis, Juvenile",D010520,82,1.33E-261
5.02E-266,147,201,"POLYDACTYLY, POSTAXIAL, WITH PROGRESSIVE MYOPIA",C536331,1,3.28E-262
5.02E-266,147,201,Premenstrual syndrome,D011293,1,3.28E-262
4.08E-265,150,219,Capillary malformation (disorder),C562760,22,2.66E-261
1.84E-265,147,202,Endemic Diseases,D019353,2,1.20E-261
1.84E-265,147,202,Vaginitis,D014627,2,1.20E-261
1.84E-265,147,202,Islet Cell Adenoma,D007516,2,1.20E-261
6.64E-265,147,203,Alcoholic Neuropathy,D020269,5,4.33E-261
1.65E-264,156,258,Leishmaniasis,D007896,64,1.07E-260
1.65E-264,156,258,Brain Lacerations,D001930,62,1.07E-260
6.64E-265,147,203,Breast Cyst,D047688,4,4.33E-261
3.52E-264,158,273,Acquired Hypogammaglobulinemia,D017074,81,2.30E-260
2.37E-264,147,204,Resistance to Insulin-Like Growth Factor I,C564816,4,1.54E-260
1.22E-263,150,222,Aphthous Stomatitis,D013281,25,7.94E-260
2.85E-263,149,217,Orchitis,D009920,20,1.86E-259
1.64E-262,162,309,Leprosy,D007918,125,1.07E-258
9.12E-262,156,265,Sicca Syndrome,D012859,71,5.94E-258
7.48E-261,151,234,"Hemorrhagic Fever, Ebola",D019142,52,4.87E-257
7.48E-261,151,234,Cutaneous Mastocytosis,D034701,41,4.87E-257
9.17E-261,153,247,Viremia,D014766,53,5.97E-257
7.06E-260,156,270,Chagas Disease,D014355,81,4.60E-256
1.07E-259,152,243,Alopecia Areata,D000506,54,6.95E-256
1.07E-259,152,243,Respiratory Tract Diseases,D012140,51,6.95E-256
7.28E-260,146,207,Schistosomiasis japonica,D012554,7,4.74E-256
3.15E-260,145,201,"Cataract, Variable Zonular Pulverulent",C565132,1,2.05E-256
8.39E-259,160,304,Uveitis,D014605,119,5.46E-255
1.34E-258,145,204,"Niemann-Pick Disease, Type B",D052537,4,8.69E-255
8.66E-258,158,291,"Dermatitis, Allergic Contact",D017449,101,5.63E-254
1.45E-257,162,325,"Tuberculosis, Pulmonary",D014397,142,9.45E-254
4.07E-257,154,263,Hay fever,D006255,75,2.64E-253
3.85E-257,147,218,Acute-On-Chronic Liver Failure,D065290,19,2.51E-253
8.42E-257,152,250,Failure to Thrive,D005183,64,5.47E-253
9.91E-257,153,257,Eosinophilic esophagitis,D057765,73,6.44E-253
1.40E-256,160,311,Pruritus,D011537,129,9.06E-253
1.89E-256,158,295,Respiratory Syncytial Virus Infections,D018357,103,1.23E-252
1.68E-256,145,208,Persistent Fetal Circulation Syndrome,D010547,9,1.09E-252
8.11E-257,144,202,Louping Ill,D008146,2,5.27E-253
4.33E-256,162,330,Hypersensitivity,D006967,158,2.81E-252
3.72E-256,148,226,Pleural Tuberculosis,D014396,29,2.41E-252
1.83E-255,158,298,Dermatomyositis,D003882,105,1.19E-251
9.02E-255,147,223,Pulmonary Eosinophilia,D011657,28,5.85E-251
9.02E-255,147,223,Anthracosis,D055008,25,5.85E-251
2.01E-254,152,256,Respiration Disorders,D012120,66,1.30E-250
2.38E-254,148,230,"Leprosy, Lepromatous",D015440,37,1.55E-250
4.30E-254,151,250,Libman-Sacks Disease,D008180,53,2.79E-250
4.90E-254,152,257,"Mastocytosis, Systemic",D034721,62,3.18E-250
4.91E-254,149,237,Russell-Silver syndrome,D056730,43,3.18E-250
7.52E-254,147,225,"Hyper-IgM Immunodeficiency Syndrome, Type 1",D053307,27,4.88E-250
1.31E-253,149,238,"Multiple Sclerosis, Acute Fulminating",D009103,42,8.48E-250
3.20E-253,158,305,Vasculitis,D014657,116,2.08E-249
3.20E-253,158,305,"Hepatitis, Autoimmune",D019693,115,2.08E-249
1.91E-253,143,203,Periodontal Pocket,D010514,3,1.24E-249
1.13E-252,144,210,MILES-CARPENTER X-LINKED MENTAL RETARDATION SYNDROME,C537472,12,7.30E-249
3.40E-252,157,300,Arthralgia,D018771,120,2.20E-248
3.98E-252,151,255,Mastocytosis,D008415,61,2.58E-248
5.21E-252,146,223,Echinococcosis,D004443,28,3.37E-248
7.49E-252,153,270,Lobar Pneumonia,D011014,75,4.85E-248
3.59E-251,147,231,Toxic Shock Syndrome,D012772,40,2.32E-247
4.17E-251,145,219,Invasive Pulmonary Aspergillosis,D055744,22,2.70E-247
9.53E-251,158,313,Chronic Periodontitis,D055113,129,6.17E-247
1.51E-250,156,297,"Diabetes, Autoimmune",D003922,100,9.79E-247
3.17E-250,156,298,Pseudohyperkalemia Cardiff,C535827,108,2.05E-246
3.11E-250,144,215,Chronic Q Fever,D011778,16,2.01E-246
9.29E-250,144,216,Eosinophilic granulomatosis with polyangiitis,D015267,18,6.01E-246
6.57E-249,143,212,"Guillain-Barre Syndrome, Familial",D020275,15,4.25E-245
6.51E-248,164,380,Graft-vs-Host Disease,D006086,197,4.21E-244
8.81E-248,147,239,Candidiasis,D002177,49,5.69E-244
8.81E-248,147,239,Toxoplasmosis,D014123,41,5.69E-244
1.49E-247,160,342,Immune thrombocytopenic purpura,D016553,155,9.62E-244
1.46E-247,149,253,Idiopathic Inflammatory Myopathies,D009220,58,9.43E-244
2.08E-247,156,307,Myocarditis,D009205,116,1.34E-243
1.94E-247,144,221,Lymphadenitis,D008199,25,1.25E-243
6.24E-247,159,335,Allergic rhinitis (disorder),D065631,149,4.03E-243
7.68E-247,162,364,Dermatitis,D003872,171,4.96E-243
1.28E-245,143,219,Sialadenitis,D012793,19,8.24E-242
4.39E-245,162,371,Lupus Nephritis,D008181,187,2.83E-241
3.63E-245,143,220,Cryoglobulinemia,D003449,24,2.35E-241
3.35E-245,142,214,Mycobacterium avium-intracellulare Infection,D015270,15,2.16E-241
4.52E-244,145,235,Confusion,D003221,42,2.91E-240
8.14E-244,151,278,Sweating,D013546,88,5.25E-240
8.14E-244,151,278,Hyperhidrosis disorder,D006945,88,5.25E-240
1.42E-242,140,208,Amebiasis,D000562,11,9.18E-239
2.32E-241,161,376,Nasal Polyps,D009298,202,1.49E-237
2.77E-241,139,205,"Pneumonia, Viral",D011024,5,1.79E-237
1.92E-240,155,322,Periodontal Diseases,D010510,127,1.24E-236
2.15E-240,143,231,End Stage Liver Disease,D058625,37,1.38E-236
2.92E-240,142,225,Ileitis,D007079,28,1.88E-236
9.35E-240,140,214,Rosacea,D012393,19,6.02E-236
7.74E-240,139,208,Chronic periaortitis,D012185,8,4.99E-236
7.01E-239,141,222,Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis,D056648,22,4.52E-235
6.78E-238,157,350,Eosinophilia,D004802,168,4.37E-234
1.64E-237,139,213,Meningoencephalitis,D008590,16,1.06E-233
4.67E-237,139,214,Polymyalgia Rheumatica,D011111,14,3.01E-233
1.02E-236,150,292,Giant Cell Arteritis,D013700,98,6.59E-233
2.26E-236,157,356,Hashimoto Disease,D050031,165,1.46E-232
2.66E-236,137,204,Vaginal Diseases,D014623,8,1.71E-232
8.48E-236,155,339,Dengue Fever,D003715,151,5.46E-232
1.30E-235,160,390,Immune System Diseases,D007154,218,8.35E-232
3.47E-235,162,414,Behcet Syndrome,D001528,230,2.23E-231
2.84E-235,138,212,Latent Autoimmune Diabetes in Adults,D000071698,14,1.82E-231
1.13E-234,165,452,Ankylosing spondylitis,D013167,292,7.25E-231
2.07E-234,139,220,"Lupus Erythematosus, Subacute Cutaneous",D008178,21,1.33E-230
4.97E-235,136,201,Splenic Infarction,D013159,1,3.20E-231
2.25E-234,138,214,Ileal Diseases,D007077,16,1.45E-230
1.36E-233,160,399,Hepatitis A,D006506,226,8.74E-230
1.95E-233,163,434,Bacterial Infections,D001424,250,1.25E-229
1.25E-232,142,244,"Bronchitis, Chronic",D029481,56,8.03E-229
2.57E-232,135,201,Duodenogastric Reflux,D004383,1,1.65E-228
7.73E-232,135,202,"Neutropenia, Nonimmune Chronic Idiopathic, Adult",C564320,2,4.97E-228
7.28E-231,166,485,Encephalomyelitis,D004679,313,4.67E-227
1.20E-230,163,448,Celiac Disease,D002446,272,7.69E-227
6.22E-230,136,212,Parainfluenza,D018184,14,3.99E-226
2.45E-229,153,345,Myasthenia Gravis,D009157,154,1.57E-225
5.50E-229,158,398,"Hepatitis B, Chronic",D019694,210,3.53E-225
4.68E-229,136,214,Pyoderma Gangrenosum,D017511,18,3.01E-225
3.80E-229,134,202,furuncle,D005667,3,2.44E-225
2.35E-228,133,198,"Impairment, Light Touch Sensation",D020886,2,1.51E-224
2.20E-227,164,478,Graves Disease,D006111,293,1.41E-223
2.68E-227,170,563,Eczema,D004485,400,1.72E-223
7.03E-227,138,232,Middle Cerebral Artery Thrombosis,D020244,33,4.51E-223
1.66E-226,136,220,"Hemorrhagic Fevers, Viral",D006482,25,1.06E-222
2.11E-226,139,240,Neuromyelitis Optica,D009471,42,1.35E-222
2.09E-226,134,208,Pelvic Pain,D017699,8,1.34E-222
9.06E-226,143,271,Rheumatism,D012216,84,5.81E-222
5.20E-226,133,203,Meningism,D008580,3,3.33E-222
1.19E-224,133,206,Viral Encephalitis,D018792,10,7.59E-221
7.54E-224,138,240,Drug Allergy,D004342,41,4.83E-220
2.58E-222,156,407,Leukopenia,D007970,224,1.65E-218
1.53E-222,134,217,"Dermatitis, Irritant",D017453,22,9.78E-219
1.85E-222,132,205,"Uveitis, Intermediate",D015867,5,1.18E-218
1.01E-221,134,219,Respiratory Hypersensitivity,D012130,20,6.48E-218
1.01E-221,134,219,Amebic colitis,D004404,19,6.48E-218
6.00E-220,153,385,Vitiligo,D014820,208,3.84E-216
2.82E-220,131,204,"Arthritis, Suppurative",D001170,4,1.81E-216
5.94E-220,133,217,Herpes encephalitis,D020803,18,3.80E-216
1.17E-219,146,317,Sezary Syndrome,D012751,127,7.46E-216
1.02E-219,134,224,Anterior uveitis,D014606,24,6.49E-216
1.52E-219,133,218,Listeriosis,D008088,21,9.69E-216
3.85E-219,133,219,Bronchitis,D001991,20,2.46E-215
2.84E-218,156,427,Myeloproliferative disease,D009196,244,1.82E-214
1.56E-218,131,208,Diffuse panbronchiolitis,C536174,11,9.94E-215
4.03E-218,137,249,Chronic Fatigue Syndrome,D015673,55,2.57E-214
7.52E-217,131,212,Dyspareunia,D004414,13,4.80E-213
8.57E-217,130,206,Congenital amegakaryocytic thrombocytopenia,C535982,6,5.47E-213
2.41E-216,142,294,"Abortion, Tubal",D000022,102,1.54E-212
6.41E-216,151,382,Sarcoidosis,D012507,198,4.09E-212
9.05E-216,158,465,Hepatitis,D006505,283,5.78E-212
9.79E-216,162,519,Dermatologic disorders,D012871,362,6.25E-212
2.28E-216,129,201,Pulmonary renal syndrome,C538458,1,1.46E-212
1.46E-215,134,235,Diffuse Scleroderma,D045743,36,9.30E-212
1.14E-213,155,439,Lupus Vulgaris,D008177,248,7.30E-210
8.05E-213,135,250,White Blood Cell Count procedure,D007958,89,5.14E-209
6.04E-212,165,589,Inflammation,D007249,402,3.85E-208
1.01E-211,129,212,Nephropathic cystinosis,D003554,15,6.43E-208
1.25E-211,128,206,Pericarditis,D010493,6,7.96E-208
4.09E-210,169,670,Tuberculosis,D014376,511,2.61E-206
2.17E-210,128,209,Small Fiber Neuropathy,D000071075,11,1.38E-206
4.10E-210,137,274,Henoch-Schoenlein Purpura,D011695,84,2.61E-206
2.17E-210,128,209,Ocular Toxoplasmosis,D014126,9,1.38E-206
7.26E-210,152,423,Acute Coronary Syndrome,D054058,234,4.62E-206
9.20E-210,159,514,"Hepatitis C, Chronic",D019698,324,5.86E-206
2.52E-210,127,203,Myeloperoxidase Deficiency,C562864,3,1.61E-206
1.15E-209,155,461,"Lupus Erythematosus, Discoid",D008179,270,7.35E-206
2.29E-209,169,676,Influenza,D007251,510,1.46E-205
2.45E-209,141,311,Monoclonal Gammopathy of Undetermined Significance,D008998,125,1.56E-205
5.21E-209,164,594,Septicemia,D018805,416,3.31E-205
5.70E-209,129,219,Cryopyrin-Associated Periodic Syndromes,D056587,19,3.63E-205
5.75E-208,162,570,Malaria,D008288,414,3.66E-204
1.32E-208,126,201,Inhalational anthrax,C571912,2,8.42E-205
1.32E-208,126,201,"Bronchiolitis, Proliferative",D001989,1,8.42E-205
1.32E-208,126,201,Spirochaetales Infections,D013145,1,8.42E-205
1.32E-208,126,201,Pontiac Fever,D007877,1,8.42E-205
1.32E-208,126,201,"Salmonella Infections, Animal",D012481,1,8.42E-205
1.32E-208,126,201,Perceptual Disorders,D010468,1,8.42E-205
4.73E-207,152,438,Juvenile arthritis,D001171,285,3.01E-203
2.39E-207,126,204,Joint Tuberculosis,D014394,5,1.52E-203
6.18E-207,126,205,Leukocyte-Adhesion Deficiency Syndrome,D018370,6,3.93E-203
1.70E-206,147,383,Severe Combined Immunodeficiency,D016511,195,1.08E-202
4.86E-206,180,939,Ulcerative Colitis,D003093,783,3.08E-202
1.58E-206,126,206,Bronchopulmonary Aspergillosis,D055732,6,1.01E-202
4.78E-206,125,201,"DIABETES MELLITUS, INSULIN-DEPENDENT, 12",C563326,1,3.03E-202
3.64E-205,139,309,Measles,D008457,121,2.31E-201
1.25E-205,125,202,Farmer's Lung,D005203,2,7.92E-202
5.67E-205,128,223,Drug Eruptions,D003875,23,3.60E-201
6.35E-205,126,210,Clostridium difficile infection,D003015,15,4.03E-201
8.31E-205,125,204,Lattice corneal dystrophy Type I,C537881,4,5.27E-201
3.04E-204,128,225,"Biliary Cirrhosis, Secondary",D008105,32,1.93E-200
1.22E-202,144,369,"Arthritis, Psoriatic",D015535,184,7.76E-199
1.70E-202,129,237,Gonorrhea,D006069,47,1.08E-198
7.16E-202,164,648,Infection,D007239,460,4.54E-198
1.23E-201,153,482,Osteopenia,D001851,312,7.82E-198
1.71E-201,126,219,Pouchitis,D019449,19,1.09E-197
5.75E-201,163,638,"Fibrosis, Liver",D008103,473,3.64E-197
1.51E-200,177,926,Crohn Disease,D003424,786,9.55E-197
2.42E-200,168,734,Arthritis,D001168,572,1.53E-196
1.07E-200,124,208,"Hypoxia-Ischemia, Brain",D020925,8,6.81E-197
1.07E-200,124,208,Ileal Pouches,D039021,8,6.81E-197
2.98E-200,136,301,Arthropathy,D007592,112,1.88E-196
5.88E-200,145,393,Epstein-Barr Virus Infections,D020031,208,3.72E-196
6.87E-200,164,664,Systemic Scleroderma,D012595,502,4.35E-196
5.83E-200,143,371,Lymphoproliferative Disorders,D008232,184,3.69E-196
1.43E-200,123,202,Primary Graft Dysfunction,D055031,2,9.06E-197
3.61E-200,123,203,"Syphilis, secondary",C536773,3,2.29E-196
3.61E-200,123,203,Mycoplasma pneumonia,D011019,3,2.29E-196
5.56E-199,123,206,"Congenital disorder of glycosylation, type 2C",C535755,7,3.52E-195
1.36E-198,123,207,Nematode infections,D009349,8,8.63E-195
1.83E-198,122,201,Inflammatory Bowel Disease 16,C567380,1,1.16E-194
4.60E-198,122,202,Ruptured Appendicitis,D001064,2,2.91E-194
4.60E-198,122,202,"HYPER-IgM IMMUNODEFICIENCY, X-LINKED, WITH ECTODERMAL DYSPLASIA, HYPOHIDROTIC",C564542,2,2.91E-194
2.81E-197,166,723,Colitis,D003092,551,1.78E-193
3.45E-197,176,939,Inflammatory Bowel Diseases,D015212,788,2.18E-193
3.84E-197,128,246,Tracheal Diseases,D014133,61,2.42E-193
1.02E-196,133,288,Lyme Disease,D008193,107,6.43E-193
1.44E-196,138,335,Pre-Eclampsia,D011225,141,9.09E-193
6.65E-196,141,369,Liver Dysfunction,D008107,191,4.20E-192
4.60E-195,136,322,Thyroid Diseases,D013959,133,2.91E-191
5.44E-195,138,342,Acquired Immunodeficiency Syndrome,D000163,155,3.43E-191
8.00E-195,139,353,"Hepatitis, Chronic",D006521,162,5.05E-191
3.53E-195,121,203,Temporomandibular Joint Dysfunction Syndrome,D013706,6,2.23E-191
3.53E-195,121,203,Autoimmune enteropathy,C538273,4,2.23E-191
3.53E-195,121,203,Elephantiasis,D004604,4,2.23E-191
3.53E-195,121,203,Linear Scleroderma,D012594,4,2.23E-191
3.53E-195,121,203,"Polychondritis, Relapsing",D011081,3,2.23E-191
4.03E-194,124,226,Craniorachischisis,D009436,34,2.54E-190
2.10E-194,121,205,Endometritis,D004716,5,1.32E-190
9.53E-194,135,318,"Lung Diseases, Interstitial",D017563,133,6.01E-190
2.18E-193,145,428,Cytomegalovirus Infections,D003586,242,1.37E-189
1.21E-193,121,207,Multi-centric Castleman's Disease,C537372,9,7.63E-190
3.48E-193,128,259,Lymphocyte Count measurement,D018655,91,2.19E-189
3.88E-193,122,215,Candidemia,D058387,19,2.44E-189
1.76E-193,120,201,Somatization Disorder,D013001,1,1.11E-189
1.76E-193,120,201,"Tinnitus, Tensor Palatini Induced",D014012,1,1.11E-189
1.76E-193,120,201,Posterior Ischemic Optic Neuropathy,D018917,1,1.11E-189
1.76E-193,120,201,Colicky Pain,D015746,1,1.11E-189
6.81E-193,121,209,Burning Mouth Syndrome,D002054,10,4.29E-189
4.31E-193,120,202,Eales disease,C538011,2,2.71E-189
3.74E-192,164,731,Immunologic Deficiency Syndromes,D007153,573,2.35E-188
1.05E-192,120,203,Salpingitis,D012488,3,6.60E-189
8.27E-192,129,272,"Malaria, Cerebral",D016779,80,5.20E-188
2.76E-191,164,739,Chronic Obstructive Airway Disease,D029424,594,1.74E-187
1.45E-191,120,206,Infantile Colic,D003085,7,9.13E-188
7.66E-191,157,617,Herpes Simplex Infections,D006561,454,4.82E-187
3.44E-191,120,207,MYD88 Deficiency,C567379,7,2.16E-187
1.05E-190,138,362,Polycythemia Vera,D011087,182,6.57E-187
1.01E-189,120,211,Congenital emphysema,C535735,12,6.36E-186
1.28E-188,121,221,Melioidosis,D008554,23,8.04E-185
4.61E-188,169,876,HIV Infections,D015658,716,2.90E-184
2.20E-188,119,208,Ectromelia,D004480,9,1.38E-184
2.09E-187,177,1083,Autoimmune Diseases,D001327,926,1.31E-183
3.54E-188,118,202,Endotoxin Hyporesponsiveness,C566417,2,2.23E-184
1.99E-187,118,204,Neurosyphilis,D009494,4,1.25E-183
1.99E-187,118,204,"Pregnancy Complications, Cardiovascular",D011249,4,1.25E-183
1.99E-187,118,204,Chlamydia pneumoniae Infections,D023521,4,1.25E-183
2.51E-186,118,207,Gram-Positive Bacterial Infections,D016908,7,1.58E-182
7.13E-186,127,277,Thyroid associated opthalmopathies,D049970,88,4.47E-182
2.56E-185,167,861,Hepatitis B,D006509,712,1.61E-181
2.36E-184,170,941,Virus Diseases,D014777,776,1.48E-180
6.86E-184,131,322,Lymphopenia,D008231,127,4.31E-180
1.15E-183,148,530,Lung diseases,D008171,354,7.24E-180
2.74E-183,133,345,Neutropenia,D009503,159,1.72E-179
5.31E-183,165,842,Hepatitis C,D006526,673,3.33E-179
2.56E-183,116,202,"Candidiasis, Familial, 2",C537979,2,1.60E-179
2.56E-182,126,282,Meningitis,D008581,86,1.60E-178
3.14E-182,116,205,Popliteal pterygium syndrome,C562509,7,1.97E-178
7.18E-182,128,302,"Encephalitis, St. Louis",D004674,111,4.50E-178
7.14E-182,116,206,Majeed syndrome,C537839,8,4.48E-178
1.80E-181,117,214,Meningococcal meningitis,D008585,14,1.13E-177
1.62E-181,116,207,Nephropathia Epidemica,D006480,7,1.01E-177
2.11E-180,124,272,Myalgia,D063806,89,1.32E-176
3.36E-180,131,339,Nephritis,D009393,146,2.10E-176
6.50E-180,152,622,Anemia,D000740,444,4.07E-176
7.61E-180,134,373,Exanthema,D005076,198,4.76E-176
3.42E-180,115,204,Fetal Diseases,D005315,8,2.14E-176
3.42E-180,115,204,IRAK4 Deficiency,C564352,4,2.14E-176
7.76E-180,115,205,Bacteriuria,D001437,5,4.86E-176
2.99E-178,135,393,Periodontitis,D010518,204,1.87E-174
1.62E-178,114,202,"Invasive Pneumococcal Disease, Recurrent Isolated, 1",C563662,2,1.02E-174
1.37E-177,127,311,Mycoses,D009181,125,8.57E-174
8.30E-178,114,204,Acanthamoeba Keratitis,D015823,5,5.19E-174
2.19E-177,123,275,"Malaria, Falciparum",D016778,79,1.37E-173
2.48E-177,119,242,Thrombocytosis,D013922,47,1.55E-173
4.20E-177,121,259,"Multiple Sclerosis, Relapsing-Remitting",D020529,64,2.62E-173
9.18E-177,114,207,Gram-Negative Bacterial Infections,D016905,8,5.73E-173
2.99E-176,128,327,Familial lichen amyloidosis,C562643,137,1.87E-172
1.25E-175,118,240,Gingivitis,D005891,47,7.81E-172
3.44E-175,126,312,Mucocutaneous Lymph Node Syndrome,D009080,130,2.15E-171
1.95E-175,113,204,Klebsiella Infections,D007710,4,1.22E-171
8.66E-175,158,781,MYELODYSPLASTIC SYNDROME,D009190,606,5.40E-171
1.81E-173,127,330,Coinfection,D060085,149,1.13E-169
4.07E-174,112,201,Eumycetoma,D008271,1,2.54E-170
4.07E-174,112,201,Acute Bacterial Prostatitis,D011472,1,2.54E-170
4.07E-174,112,201,Chronic malaria,C531736,1,2.54E-170
1.91E-173,114,217,Chediak-Higashi Syndrome,D002609,19,1.19E-169
1.28E-172,119,259,Keratitis,D007634,66,7.98E-169
2.13E-171,112,209,Schnitzler Syndrome,D019873,9,1.33E-167
1.92E-170,150,670,Steatohepatitis,D005234,500,1.20E-166
9.60E-171,112,211,"Toxoplasmosis, Congenital",D014125,12,5.99E-167
1.33E-169,166,1025,Degenerative polyarthritis,D010003,868,8.32E-166
1.89E-169,122,299,Gingival Diseases,D005882,105,1.18E-165
2.91E-169,170,1137,Arteriosclerosis,D001161,968,1.82E-165
9.72E-169,175,1294,Asthma,D001249,1153,6.06E-165
9.56E-169,171,1173,Atherosclerosis,D050197,1005,5.95E-165
3.26E-168,112,219,Colonic Diseases,D003108,21,2.03E-164
1.17E-167,136,471,Malignant mesothelioma,C562839,304,7.26E-164
2.04E-167,110,207,Food Allergy,D005512,8,1.27E-163
8.71E-167,126,353,Gastritis,D005756,157,5.42E-163
1.67E-166,120,293,Synovitis,D013585,100,1.04E-162
1.51E-166,111,217,Endophthalmitis,D009877,18,9.42E-163
3.48E-166,119,285,Bronchiectasis,D001987,95,2.16E-162
6.49E-166,117,268,Severe Acute Respiratory Syndrome,D045169,78,4.04E-162
2.72E-165,128,384,Glomerulonephritis,D005921,193,1.69E-161
4.36E-165,125,351,Primary Myelofibrosis,D055728,166,2.71E-161
1.19E-164,184,1693,Rheumatoid Arthritis,D001172,1566,7.36E-161
9.14E-165,108,201,Cold Hemagglutinin Disease,D000744,2,5.68E-161
9.14E-165,108,201,Pulmonary Histiocytosis X,D006646,1,5.68E-161
9.14E-165,108,201,Familial Waldenstrom's Macroglobulinaemia,D008258,1,5.68E-161
1.62E-163,140,561,Cirrhosis,D005355,387,1.00E-159
2.14E-163,114,252,Spondylarthropathies,D025242,55,1.33E-159
8.01E-163,108,207,"COPPER TOXICOSIS, IDIOPATHIC",C565846,9,4.98E-159
1.67E-162,113,247,Acne,D000152,55,1.03E-158
5.08E-162,121,324,Cachexia,D002100,134,3.15E-158
6.75E-162,117,285,Enterovirus Infections,D004769,91,4.19E-158
6.75E-162,117,285,Polymyositis,D017285,90,4.19E-158
3.89E-162,107,202,Staphylococcal Skin Infections,D013207,2,2.42E-158
6.63E-161,116,280,Rhinitis,D012220,90,4.11E-157
7.37E-161,107,206,Delayed Graft Function,D051799,6,4.57E-157
1.52E-160,107,207,Raynaud Disease,D011928,8,9.41E-157
1.64E-159,129,432,Idiopathic pulmonary arterial hypertension,D065627,257,1.02E-155
2.24E-159,126,395,IGA Glomerulonephritis,D005922,210,1.39E-155
5.27E-159,115,279,Dejerine-Sottas Disease (disorder),D015417,86,3.27E-155
1.30E-158,142,637,Hyperglycemia,D006943,458,8.07E-155
6.94E-159,108,220,Idiopathic Interstitial Pneumonias,D054988,22,4.30E-155
1.56E-158,112,254,Urinary tract infection,D014552,63,9.64E-155
1.86E-157,109,233,Monoclonal Gammapathies,D010265,39,1.15E-153
2.72E-157,113,268,Hypogammaglobulinemia,D000361,77,1.68E-153
1.15E-156,137,570,"Kidney Failure, Chronic",D007676,394,7.12E-153
2.49E-156,117,311,Depressive Symptoms,D003863,130,1.54E-152
4.46E-156,108,230,Painful Bladder Syndrome,D018856,33,2.76E-152
3.97E-155,105,210,"Leprosy, Paucibacillary",D056005,14,2.46E-151
3.97E-155,105,210,"Pyogenic Arthritis, Pyoderma Gangrenosum and Acne",C536253,14,2.46E-151
8.80E-155,131,493,Thrombocytopenia,D013921,317,5.45E-151
3.27E-154,108,237,"Sleep Apnea, Central",D020182,44,2.02E-150
6.95E-154,123,392,Pancreatitis,D010195,205,4.30E-150
6.79E-154,113,283,Pleural effusion disorder,D010996,95,4.20E-150
1.15E-153,105,215,Central Nervous System Infection,D002494,15,7.12E-150
2.23E-153,121,371,Thymoma,D013945,187,1.38E-149
2.85E-153,110,258,Diphtheria,D004165,64,1.76E-149
1.71E-153,104,208,Macrophage Activation Syndrome,D055501,11,1.06E-149
5.50E-153,118,339,Irritable Bowel Syndrome,D043183,151,3.40E-149
2.50E-152,110,262,Spondylarthritis,D025241,69,1.55E-148
3.88E-151,102,201,Snowflake vitreoretinal degeneration,C536677,4,2.40E-147
1.31E-150,117,341,Fever,D005334,159,8.10E-147
1.85E-150,108,252,Osteomyelitis,D010019,57,1.14E-146
2.07E-150,106,235,Congenital neutropenia,C537592,40,1.28E-146
3.74E-150,106,236,Optic Neuritis,D009902,38,2.31E-146
4.91E-150,107,245,Rotavirus Infections,D012400,49,3.03E-146
7.88E-150,103,213,Paracoccidioidomycosis,D010229,14,4.87E-146
1.21E-149,106,238,Immunoglobulin A deficiency (disorder),D017098,47,7.44E-146
1.56E-149,109,265,Thalassemia,D013789,72,9.65E-146
2.88E-149,103,215,"Aspergillosis, Allergic Bronchopulmonary",D001229,18,1.78E-145
2.36E-149,102,207,Tuberculoid leprosy,D015441,7,1.46E-145
4.83E-149,108,258,Cooley's anemia,D017086,60,2.98E-145
4.93E-149,105,232,Infectious Mononucleosis,D007244,35,3.04E-145
5.58E-149,104,224,"Meningitis, Pneumococcal",D008586,25,3.44E-145
1.22E-147,102,213,Balkan Nephropathy,D001449,14,7.50E-144
2.77E-147,112,305,Mycosis Fungoides,D009182,116,1.71E-143
8.05E-147,103,224,Extrinsic allergic alveolitis,D000542,24,4.96E-143
1.19E-145,111,303,CNS disorder,D002493,114,7.33E-142
1.52E-145,106,255,Necrotizing Enterocolitis,D020345,59,9.35E-142
2.10E-145,120,409,Hypercholesterolemia,D006937,226,1.30E-141
1.61E-145,103,229,Abscess,D000038,32,9.90E-142
2.57E-145,106,256,Systemic Inflammatory Response Syndrome,D018746,60,1.59E-141
5.19E-145,103,231,Lichen Planus,D008010,34,3.20E-141
1.50E-144,161,1264,Epithelial ovarian cancer,C538090,1124,9.25E-141
1.63E-144,116,365,Tuberous Sclerosis,D014402,175,1.00E-140
1.65E-144,103,233,Rabies (disorder),D011818,44,1.02E-140
4.53E-144,136,671,Metabolic Syndrome X,D024821,497,2.78E-140
2.23E-144,101,217,Mastitis,D008413,20,1.37E-140
3.72E-144,102,226,Alveolar Bone Loss,D016301,27,2.29E-140
3.28E-144,99,202,"Surfactant Metabolism Dysfunction, Pulmonary, 4",C567461,2,2.02E-140
2.17E-143,144,841,Cerebrovascular accident,D020521,676,1.33E-139
2.74E-143,167,1481,Diabetes Mellitus,D003920,1331,1.69E-139
2.86E-143,117,385,Hamman-Rich syndrome,D011658,199,1.76E-139
1.26E-142,131,596,Myocardial Ischemia,D017202,410,7.74E-139
4.04E-142,105,261,"Pleural Effusion, Malignant",D016066,67,2.48E-138
3.14E-142,100,217,Heat Stroke,D018883,17,1.93E-138
2.29E-141,141,801,Hyperactive behavior,D006948,647,1.41E-137
2.58E-142,98,201,"Charcot-Marie-Tooth disease, Type 2D",C537993,1,1.59E-138
2.47E-141,124,495,Idiopathic Pulmonary Fibrosis,D054990,326,1.51E-137
2.04E-141,102,237,"Sarcoidosis, Pulmonary",D017565,38,1.25E-137
2.99E-141,109,305,Reperfusion Injury,D015427,107,1.83E-137
1.52E-140,106,278,Retroviridae Infections,D012192,83,9.34E-137
2.35E-140,115,379,Nonalcoholic Steatohepatitis,D065626,191,1.44E-136
1.84E-140,102,241,"Arthritis, Adjuvant-Induced",D001169,41,1.13E-136
2.04E-140,100,224,Carotid Artery Plaque,D016893,24,1.25E-136
3.15E-140,102,242,Peptic Esophagitis,D004942,43,1.94E-136
6.84E-140,142,841,Coronary Arteriosclerosis,D003324,678,4.19E-136
4.80E-140,101,234,Salmonella infections,D012480,36,2.94E-136
7.87E-140,113,358,Cervical Intraepithelial Neoplasia,D018290,190,4.82E-136
1.16E-139,100,227,Periapical Periodontitis,D010485,30,7.10E-136
1.50E-139,105,273,DOSAGE-SENSITIVE SEX REVERSAL,C535601,82,9.17E-136
1.42E-139,99,219,Allergic Conjunctivitis,D003233,19,8.69E-136
6.38E-139,143,876,Cardiovascular Diseases,D002318,705,3.91E-135
2.81E-139,98,212,Hyperimmunoglobulin M syndrome,D053306,12,1.72E-135
1.29E-138,102,249,Lymphocytosis,D008218,50,7.87E-135
9.41E-139,97,206,"Keratitis, Herpetic",D016849,7,5.77E-135
1.73E-138,98,215,Bone Marrow failure syndromes,C536572,18,1.06E-134
1.73E-138,98,215,Typhoid Fever,D014435,17,1.06E-134
1.76E-138,97,207,"Rhinitis, Allergic, Perennial",D012221,7,1.08E-134
1.18E-137,107,303,Uterine Cervical Neoplasm,D002583,115,7.21E-134
2.23E-137,116,412,Splenomegaly,D013163,233,1.36E-133
1.99E-137,96,203,"Corpus Callosum, Agenesis of, with Facial Anomalies and Robin Sequence",C563127,3,1.22E-133
1.45E-136,101,249,Cystitis,D003556,50,8.90E-133
2.36E-136,99,232,"Meningitis, Bacterial",D016920,33,1.44E-132
2.27E-136,97,215,Pleocytosis,D007964,15,1.39E-132
4.04E-136,101,251,"Lichen Planus, Oral",D017676,52,2.47E-132
2.41E-136,96,207,Cutaneous Candidiasis,D002179,8,1.47E-132
2.41E-136,96,207,Panuveitis,D015864,7,1.47E-132
9.47E-136,165,1564,"Diabetes Mellitus, Non-Insulin-Dependent",D003924,1432,5.79E-132
1.01E-135,104,282,Prolactinoma,D015175,86,6.19E-132
2.07E-135,100,245,"Cockayne Syndrome, Type I",D003057,49,1.27E-131
7.85E-136,95,201,"Sexually Transmitted Diseases, Bacterial",D015231,1,4.80E-132
7.85E-136,95,201,Septic Toxemia,D014115,1,4.80E-132
7.85E-136,95,201,"Meningitis, Listeria",D008584,1,4.80E-132
1.47E-135,95,202,Lichenoid Eruptions,D017512,2,8.99E-132
1.47E-135,95,202,"Eye Infections, Bacterial",D015818,2,8.99E-132
6.05E-135,102,266,Hemophilia A,D006467,80,3.69E-131
5.41E-135,98,229,Subacute Sclerosing Panencephalitis,D013344,31,3.30E-131
4.96E-135,96,212,Group B Streptococcal Infection,D013290,14,3.03E-131
5.11E-135,95,204,Tularemia,D014406,6,3.12E-131
9.47E-135,95,205,Neuropsychiatric Systemic Lupus Erythematosus,D020945,5,5.78E-131
2.30E-134,97,223,Staphylococcus aureus infection,D013203,26,1.40E-130
5.68E-134,116,437,polyps,D011127,261,3.46E-130
9.18E-134,101,262,Osteitis Deformans,D010001,67,5.60E-130
1.94E-133,95,210,Hashimoto's encephalitis,C535841,12,1.18E-129
1.99E-133,94,202,Ehrlichiosis,D016873,3,1.21E-129
7.84E-133,106,319,Monosomy,D009006,133,4.78E-129
1.99E-133,94,202,Urinary Bladder Calculi (disorder),D001744,2,1.21E-129
1.77E-132,111,381,Blast Phase,D001752,196,1.08E-128
1.69E-132,104,299,"Anemia, Hemolytic",D000743,102,1.03E-128
6.79E-133,94,204,"Interleukin 2 Receptor, Alpha, Deficiency of",C565232,4,4.14E-129
1.91E-132,98,240,Thyroiditis,D013966,41,1.17E-128
4.15E-132,94,207,"Tuberculosis, Multidrug-Resistant",D018088,11,2.52E-128
4.15E-132,94,207,Keratoconjunctivitis,D007637,10,2.52E-128
1.56E-131,97,235,Delirium,D003693,41,9.49E-128
2.44E-131,94,210,Mucocutaneous leishmaniasis,D007897,12,1.49E-127
4.43E-131,97,237,Exfoliative dermatitis,D003873,42,2.69E-127
5.33E-131,99,256,Schistosomiasis,D012552,58,3.24E-127
6.10E-131,95,220,Adult-Onset Still Disease,D016706,20,3.71E-127
1.42E-131,93,201,Inflammatory Bowel Disease 17,C567378,1,8.65E-128
1.80E-130,98,249,Bullous pemphigoid,D010391,54,1.09E-126
1.59E-130,93,205,Hyperimmunoglobulinemia D,D054078,7,9.69E-127
3.82E-130,100,270,Demyelinating Diseases,D003711,78,2.32E-126
1.59E-130,93,205,Actinic prurigo,C566780,5,9.69E-127
6.02E-130,96,233,Acute intermittent porphyria,D017118,38,3.65E-126
5.21E-130,93,207,Lown-Ganong-Levine Syndrome,D008151,7,3.16E-126
9.49E-130,95,225,Myxoma,D009232,29,5.76E-126
1.33E-129,101,283,Biliary Atresia,D001656,92,8.09E-126
1.63E-129,102,294,Disorder of eye,D005128,119,9.91E-126
9.35E-130,93,208,"Toxoplasmosis, Cerebral",D016781,8,5.68E-126
1.34E-129,94,217,Prune Belly Syndrome,D011535,18,8.13E-126
3.62E-129,100,275,Subarachnoid Hemorrhage,D013345,82,2.20E-125
8.80E-129,103,309,"Hamartoma Syndrome, Multiple",D006223,122,5.33E-125
8.54E-129,98,257,Dysplastic Nevus,D004416,64,5.18E-125
7.07E-129,94,220,Herpesviridae Infections,D006566,23,4.29E-125
7.07E-129,94,220,Dyspepsia,D004415,22,4.29E-125
1.83E-129,92,201,"METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblF TYPE (disorder)",C564747,1,1.11E-125
1.22E-128,94,221,Enterocolitis,D004760,23,7.41E-125
1.95E-128,103,311,Hyperplasia,D006965,114,1.18E-124
3.49E-128,98,260,Bronchial Hyperreactivity,D016535,66,2.12E-124
6.35E-128,92,207,Eye Infections,D015817,9,3.85E-124
8.89E-128,93,216,Pneumoconiosis,D011009,19,5.39E-124
6.35E-128,92,207,"Shock, Hemorrhagic",D012771,7,3.85E-124
1.06E-127,94,225,Chronic Kidney Insufficiency,D051436,27,6.40E-124
1.55E-127,93,217,Pleurisy,D010998,18,9.36E-124
2.68E-127,93,218,"Skin Diseases, Infectious",D012874,21,1.62E-123
2.68E-127,93,218,Otitis Media with Effusion,D010034,20,1.62E-123
4.99E-127,95,237,Synovial Cyst,D013581,45,3.02E-123
3.55E-127,92,210,Endotoxemia,D019446,10,2.15E-123
9.36E-127,118,528,Hyperinsulinism,D006946,350,5.66E-123
1.43E-126,142,1031,Myocardial Infarction,D009203,877,8.64E-123
8.25E-127,95,238,Thromboangiitis Obliterans,D013919,43,4.99E-123
1.10E-126,92,212,Immune Reconstitution Inflammatory Syndrome,D054019,12,6.64E-123
1.81E-126,96,249,Gastrointestinal Hemorrhage,D006471,57,1.10E-122
2.09E-126,97,259,"Angina, Unstable",D000789,61,1.26E-122
7.45E-127,91,203,INTERLEUKIN 1 RECEPTOR ANTAGONIST DEFICIENCY,C557815,3,4.51E-123
1.92E-126,92,213,Erythema Chronicum Migrans,D015787,16,1.16E-122
2.33E-126,93,222,"Apraxia, Developmental Verbal",D001072,22,1.41E-122
4.84E-126,111,428,Refractory anemias,D000753,248,2.92E-122
4.08E-126,94,232,Bacterial Vaginosis,D016585,36,2.47E-122
3.35E-126,92,214,Diffuse cutaneous leishmaniasis,D016774,15,2.02E-122
7.56E-126,96,252,Meningococcal Infections,D008589,57,4.56E-122
6.80E-126,94,233,Systemic candidiasis,C536777,36,4.11E-122
4.25E-126,91,206,HIV Wasting Syndrome,D019247,6,2.57E-122
1.30E-125,105,352,Ulcer,D014456,164,7.85E-122
1.21E-125,96,253,"Hepatitis, Alcoholic",D006519,62,7.30E-122
7.53E-126,91,207,Choledochal Cyst,D015529,10,4.55E-122
1.01E-125,92,216,"Glossitis, Benign Migratory",D005929,19,6.07E-122
1.91E-125,98,274,"Osteoarthritis, Knee",D020370,81,1.15E-121
3.20E-125,97,265,Skin Ulcer,D012883,78,1.93E-121
3.08E-125,96,255,Autoimmune thyroiditis,D013967,55,1.86E-121
3.09E-125,94,236,Pelvic Inflammatory Disease,D000292,37,1.86E-121
2.98E-125,92,218,Temporomandibular Joint Disorders,D013705,21,1.80E-121
5.09E-125,94,237,"MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA",C565054,41,3.06E-121
6.98E-125,98,277,"Hypertension, Portal",D006975,87,4.20E-121
5.11E-125,92,219,Shock,D012769,20,3.08E-121
9.13E-125,93,229,Takayasu Arteritis,D013625,30,5.50E-121
1.09E-124,95,248,AICARDI-GOUTIERES SYNDROME 1,C535607,54,6.56E-121
1.34E-124,100,300,"Liver Failure, Acute",D017114,110,8.09E-121
1.37E-124,94,239,Arsenic Encephalopathy,D020261,57,8.23E-121
1.64E-124,98,279,Contact Dermatitis,D003877,84,9.87E-121
2.78E-125,90,201,"Dysentery, Bacillary",D004405,1,1.68E-121
2.78E-125,90,201,Infection of amniotic cavity,D002821,1,1.68E-121
1.52E-124,93,230,Varicose Ulcer,D014647,33,9.16E-121
1.48E-124,92,221,Keratoconjunctivitis Sicca,D007638,28,8.93E-121
4.98E-125,90,202,Combined Cellular And Humoral Immune Defects With Granulomas,C567115,2,3.00E-121
1.25E-124,91,212,"Pemphigoid, Benign Mucous Membrane",D010390,12,7.50E-121
8.89E-125,90,203,Gingival Recession,D005889,4,5.35E-121
1.58E-124,90,204,"Leukoencephalitis, Acute Hemorrhagic",D004684,4,9.50E-121
6.81E-124,125,683,Cystic Fibrosis,D003550,519,4.09E-120
4.20E-124,93,232,TNF receptor-associated periodic fever syndrome (TRAPS),C536657,35,2.52E-120
2.80E-124,90,205,"Neutropenia, severe chronic",C535815,5,1.68E-120
1.14E-123,95,253,"MYELOPROLIFERATIVE SYNDROME, TRANSIENT",C563551,57,6.84E-120
2.03E-123,102,330,TARSAL-CARPAL COALITION SYNDROME,C536943,152,1.22E-119
1.89E-123,91,217,Cervix Diseases,D002577,22,1.14E-119
1.52E-123,90,208,Osteitis,D010000,9,9.12E-120
3.75E-123,107,395,Kidney Neoplasm,D007680,213,2.25E-119
5.34E-123,110,438,Brain Ischemia,D002545,247,3.20E-119
3.38E-123,92,227,Autoimmune state,D015551,31,2.03E-119
4.02E-123,94,246,Osteopetrosis,D010022,57,2.41E-119
3.38E-123,92,227,CREST Syndrome,D017675,29,2.03E-119
5.62E-123,92,228,Malignant neoplasm of vulva,D014846,32,3.37E-119
1.03E-122,111,455,Barrett Esophagus,D001471,281,6.18E-119
1.74E-122,107,400,Brain Diseases,D001927,231,1.05E-118
1.65E-122,94,249,Chlamydia Infections,D002690,52,9.86E-119
1.55E-122,92,230,Lipoid nephrosis,D009402,32,9.27E-119
1.57E-122,91,221,Granuloma,D006099,21,9.40E-119
1.57E-122,91,221,Cancer of Digestive System,D004067,21,9.40E-119
2.73E-122,106,388,Malnutrition,D044342,211,1.63E-118
5.82E-123,89,202,Infection by Trichuris trichiura,D014257,2,3.49E-119
2.56E-122,96,270,Stable angina,D060050,73,1.53E-118
3.51E-122,93,241,Li-Fraumeni Syndrome,D016864,43,2.10E-118
4.43E-122,91,223,Condylomata Acuminata,D003218,25,2.65E-118
7.34E-122,104,365,Eclampsia,D004461,173,4.39E-118
4.06E-122,90,214,Pulpitis,D011671,16,2.43E-118
9.13E-122,93,243,Cerebral Aneurysm,D002532,50,5.46E-118
6.94E-122,90,215,Multiple Organ Failure,D009102,16,4.15E-118
1.24E-121,91,225,"Chromosome 5, trisomy 5q",C537650,29,7.40E-118
1.64E-121,94,254,"Cholestasis, Extrahepatic",D001651,57,9.84E-118
1.69E-121,89,208,Urban cutaneous leishmaniasis,D016773,9,1.01E-117
5.64E-121,91,228,Cholangitis,D002761,32,3.37E-117
7.60E-121,96,278,Retinal Detachment,D012163,88,4.54E-117
5.72E-121,90,219,Chagas Cardiomyopathy,D002598,19,3.42E-117
5.03E-121,89,210,Ear Inflammation,D010031,10,3.01E-117
9.49E-121,93,248,Silicosis,D012829,51,5.67E-117
1.67E-120,109,444,"Aortic Aneurysm, Abdominal",D017544,258,9.97E-117
1.55E-120,94,259,Duodenal Ulcer,D004381,65,9.26E-117
1.51E-120,93,249,Mycoplasma Infections,D009175,55,8.99E-117
3.76E-121,88,201,West Nile Fever Myelitis,D014901,1,2.25E-117
3.76E-121,88,201,"DIABETES MELLITUS, INSULIN-DEPENDENT, 22 (disorder)",C567284,1,2.25E-117
1.48E-120,89,212,Common Cold,D003139,14,8.83E-117
1.16E-120,88,203,Peroxisomal ACYL-COA oxidase deficiency,C536662,3,6.93E-117
2.52E-120,89,213,Thrombocytopenic purpura,D011696,13,1.51E-116
5.16E-120,100,328,Hematological Disease,D006402,143,3.08E-116
5.06E-120,95,272,Peripheral Vascular Diseases,D016491,74,3.02E-116
6.89E-120,99,317,Malignant Squamous Cell Neoplasm,D018307,132,4.10E-116
4.29E-120,89,214,Pleural Diseases,D010995,16,2.56E-116
4.29E-120,89,214,Aspergillosis,D001228,14,2.56E-116
6.67E-120,91,233,Microscopic Polyarteritis,D055953,41,3.98E-116
6.67E-120,91,233,Spinal Cord Diseases,D013118,38,3.98E-116
8.46E-120,92,243,Stevens-Johnson Syndrome,D013262,46,5.04E-116
7.45E-120,90,224,Acute Chest Syndrome,D056586,27,4.44E-116
9.30E-120,93,253,"Fibromatosis, Aggressive",D018222,57,5.54E-116
1.23E-119,90,225,Microvascular Angina,D017566,28,7.34E-116
2.00E-119,97,297,"Amyotrophic Lateral Sclerosis, Sporadic",C531617,125,1.19E-115
1.23E-119,89,216,Chronic multifocal osteomyelitis,C535456,18,7.32E-116
2.45E-119,110,469,"Kidney Failure, Acute",D058186,280,1.46E-115
1.06E-119,88,207,Pseudomonas Infections,D011552,9,6.29E-116
2.15E-119,92,245,Pneumocystis jiroveci pneumonia,D011020,52,1.28E-115
4.16E-119,118,605,Down Syndrome,D004314,434,2.47E-115
2.07E-119,89,217,Benign Mastocytoma,D034801,19,1.23E-115
2.84E-119,91,236,Idiopathic Membranous Glomerulonephritis,D015433,36,1.69E-115
1.82E-119,88,208,Persistent Polyclonal B-Cell Lymphocytosis,C564707,8,1.08E-115
1.82E-119,88,208,Oliguria,D009846,8,1.08E-115
3.56E-119,93,256,Hepatic methionine adenosyltransferase deficiency,C564683,58,2.11E-115
3.35E-119,90,227,Trigeminal Neuralgia,D014277,28,1.99E-115
3.35E-119,90,227,LEOPARD Syndrome,D044542,28,1.99E-115
5.03E-119,94,267,Van der Woude syndrome,C536528,76,2.99E-115
3.47E-119,89,218,Smallpox,D012899,19,2.06E-115
4.58E-119,91,237,PITUITARY ADENOMA PREDISPOSITION (disorder),C566321,39,2.72E-115
4.58E-119,91,237,HELLP Syndrome,D017359,39,2.72E-115
7.70E-119,94,268,Chordoma,D002817,74,4.57E-115
9.00E-119,90,229,"Polyradiculoneuropathy, Chronic Inflammatory Demyelinating",D020277,32,5.34E-115
1.18E-118,91,239,"Lymphohistiocytosis, Hemophagocytic",D051359,43,7.02E-115
1.47E-118,90,230,AIDS Dementia Complex,D015526,35,8.72E-115
2.11E-118,92,250,Paroxysmal nocturnal hemoglobinuria,D006457,57,1.25E-114
2.39E-118,90,231,"Macular dystrophy, corneal type 1",C537834,36,1.42E-114
5.08E-118,106,421,Renal Insufficiency,D051437,246,3.01E-114
3.88E-118,90,232,Malonic aciduria,C535702,38,2.30E-114
4.91E-118,93,262,Hereditary gingival fibromatosis,C562884,67,2.91E-114
5.18E-118,92,252,Carotid Artery Diseases,D002340,54,3.07E-114
3.79E-118,87,205,Neonatal Early-Onset Sepsis,D000071074,5,2.25E-114
6.52E-118,87,206,Luft Disease,D017240,7,3.86E-114
6.52E-118,87,206,Drug Hypersensitivity Syndrome,D063926,7,3.86E-114
1.91E-117,91,245,X-linked agammaglobulinemia,C537409,48,1.13E-113
1.12E-117,87,207,Avascular Necrosis of Femur Head,D005271,7,6.62E-114
2.62E-117,90,236,LIMB-MAMMARY SYNDROME,C535903,43,1.55E-113
1.91E-117,87,208,Pseudorabies,D011557,9,1.13E-113
1.91E-117,87,208,Molluscum Contagiosum,D008976,8,1.13E-113
6.79E-117,131,907,Amyloidosis,D000686,749,4.02E-113
3.46E-117,88,218,Tick-Borne Encephalitis,D004675,21,2.05E-113
6.70E-117,90,238,Abetalipoproteinemia,D000012,42,3.97E-113
5.74E-117,88,219,Fetal Alcohol Spectrum Disorders,D063647,21,3.40E-113
5.50E-117,87,210,Insulin-dependent diabetes mellitus secretory diarrhea syndrome,C580192,12,3.26E-113
8.48E-117,89,229,Avellino corneal dystrophy,C535474,33,5.02E-113
1.44E-116,101,364,Papilloma,D010212,185,8.48E-113
1.17E-116,91,249,Hantavirus Infections,D018778,52,6.89E-113
9.29E-117,87,211,Warts,D014860,17,5.50E-113
1.44E-116,93,270,Bacteremia,D016470,78,8.53E-113
9.29E-117,87,211,"Macular Edema, Cystoid",D008269,13,5.50E-113
1.72E-116,92,260,Attention Deficit Disorder,D001289,69,1.01E-112
2.22E-116,89,231,Neurocognitive Disorders,D019965,33,1.31E-112
4.52E-117,86,201,"DEAFNESS, AUTOSOMAL RECESSIVE, 24",C567027,1,2.68E-113
7.82E-117,86,202,Spastic cerebral palsy,D002547,2,4.63E-113
2.63E-116,87,213,Aortic Rupture,D001019,16,1.55E-112
7.51E-116,107,454,Epithelioma,D009375,271,4.43E-112
7.54E-116,95,296,Erythema,D004890,108,4.45E-112
7.54E-116,95,296,Urticaria,D014581,106,4.45E-112
3.96E-116,86,205,Collagenous Sprue,D064068,5,2.34E-112
9.22E-116,89,234,LATERAL MENINGOCELE SYNDROME,C537878,41,5.44E-112
9.22E-116,89,234,Hemorrhage,D006470,34,5.44E-112
1.06E-115,90,244,Familial Mediterranean Fever,D010505,50,6.23E-112
6.75E-116,86,206,Schizotypal Personality Disorder,D012569,7,3.99E-112
1.47E-115,89,235,Alcoholic Intoxication,D000435,39,8.69E-112
1.84E-115,88,226,Corneal Ulcer,D003320,29,1.08E-111
1.15E-115,86,207,Poxviridae Infections,D011213,7,6.76E-112
2.35E-115,89,236,Schwartz-Jampel Syndrome,D010009,39,1.38E-111
2.60E-115,90,246,Hemolytic-Uremic Syndrome,D006463,54,1.53E-111
3.75E-115,93,278,Edema,D004487,86,2.21E-111
1.94E-115,86,208,"Neuropathy, Painful",C564945,9,1.14E-111
1.94E-115,86,208,"Encephalomyelitis, Acute Disseminated",D004673,9,1.14E-111
3.34E-115,87,218,Incontinentia Pigmenti Achromians,D010859,25,1.97E-111
3.28E-115,86,209,Pityriasis Rubra Pilaris,D010916,10,1.93E-111
3.28E-115,86,209,Leukemic Infiltration,D017254,10,1.93E-111
1.12E-114,101,378,Addictive Behavior,D016739,196,6.59E-111
7.78E-115,88,229,AIDS related complex,D000386,37,4.58E-111
5.51E-115,86,210,Cerebral abscess,D001922,10,3.24E-111
5.51E-115,86,210,Hypersplenism,D006971,10,3.24E-111
9.39E-115,89,239,keratoacanthoma,D007636,44,5.52E-111
1.39E-114,91,260,"Chromosome 8, trisomy",C537942,63,8.19E-111
1.25E-114,88,230,Milroy Disease,D008209,33,7.35E-111
9.24E-115,86,211,Paraneoplastic Cerebellar Degeneration,D020362,12,5.43E-111
2.27E-114,112,549,"Cardiomyopathy, Dilated",D002311,376,1.33E-110
1.48E-114,89,240,Angioimmunoblastic Lymphadenopathy,D007119,43,8.71E-111
2.55E-114,94,294,"Gastritis, Atrophic",D005757,107,1.50E-110
2.85E-114,98,342,"Respiratory Distress Syndrome, Adult",D012128,156,1.67E-110
1.54E-114,86,212,Leptospirosis,D007922,13,9.07E-111
1.54E-114,86,212,Reproductive tract infection,D060737,12,9.07E-111
8.15E-115,85,202,Eosinophilic gastroenteritis,C535952,2,4.79E-111
8.15E-115,85,202,"Peritonitis, Tuberculous",D014395,2,4.79E-111
5.25E-114,121,724,Huntington Disease,D006816,551,3.08E-110
4.58E-114,97,331,"Hypercholesterolemia, Familial",D006938,143,2.68E-110
5.07E-114,101,383,Dyslipidemias,D050171,195,2.97E-110
1.39E-114,85,203,"Uveitis, Posterior",D015866,3,8.18E-111
4.27E-114,86,214,Herpes zoster disease,D006562,18,2.51E-110
4.27E-114,86,214,Syphilis,D013587,18,2.51E-110
4.27E-114,86,214,Sexually Transmitted Diseases,D012749,17,2.51E-110
4.27E-114,86,214,Invasive Fungal Infections,D000072742,16,2.51E-110
8.69E-114,93,286,Premature Obstetric Labor,D007752,96,5.09E-110
4.02E-114,85,205,Fibrous histiocytoma of tendon sheath,D000070779,5,2.36E-110
7.07E-114,86,215,Schistosomiasis mansoni,D012555,15,4.14E-110
1.30E-113,88,235,Enteritis,D004751,40,7.59E-110
6.80E-114,85,206,Leukocytoclastic vasculitis,C535509,6,3.98E-110
1.40E-113,89,245,Metaplasia,D008679,47,8.21E-110
1.96E-113,100,374,Seminoma,D018239,195,1.15E-109
1.70E-113,91,266,Alcoholic Liver Diseases,D008108,71,9.96E-110
1.17E-113,86,216,"THANATOPHORIC DYSPLASIA, TYPE I (disorder)",C566844,17,6.83E-110
1.92E-113,86,217,Pseudomyxoma Peritonei,D011553,18,1.12E-109
2.70E-113,87,227,Superinfection,D015163,29,1.58E-109
1.92E-113,85,208,Nephrogenic Fibrosing Dermopathy,D054989,8,1.13E-109
3.86E-113,91,268,Coughing,D003371,78,2.26E-109
4.18E-113,92,279,Adenovirus Infections,D000257,83,2.44E-109
3.15E-113,86,218,Neurocysticercosis,D020019,20,1.84E-109
4.76E-113,90,258,Granulomatosis with polyangiitis,D014890,65,2.78E-109
4.33E-113,87,228,5q-syndrome,C535323,32,2.53E-109
4.33E-113,87,228,AIDS-Associated Nephropathy,D016263,30,2.53E-109
4.33E-113,87,228,Infective endocarditis,D004696,30,2.53E-109
5.15E-113,86,219,Helminthiasis,D006373,22,3.01E-109
8.93E-113,85,211,Coronary Occlusion,D054059,12,5.21E-109
1.77E-112,87,231,HTLV-I Infections,D015490,32,1.03E-108
2.21E-112,86,222,Plasma Cell Neoplasm,D054219,26,1.29E-108
2.21E-112,86,222,Borna Disease,D001890,24,1.29E-108
4.85E-113,84,201,ASTHMA AND NASAL POLYPS,C565739,1,2.83E-109
4.85E-113,84,201,Cystic Periventricular Leukomalacia,D007969,1,2.83E-109
8.24E-113,84,202,Lipomatous hemangiopericytoma,C537029,2,4.81E-109
1.40E-112,84,203,Echogenic Bowel,D058535,4,8.15E-109
8.27E-112,125,842,"Liver Cirrhosis, Experimental",D008106,737,4.82E-108
2.36E-112,84,204,"Aplastic anemia, idiopathic",C538494,5,1.38E-108
4.03E-112,85,214,Stenosis,D003251,15,2.35E-108
2.36E-112,84,204,"Tuberculosis, Miliary",D014391,4,1.38E-108
3.97E-112,84,205,Pneumocystis Infections,D016720,7,2.31E-108
9.26E-112,86,225,Paget Disease Extramammary,D010145,27,5.40E-108
6.65E-112,84,206,"Meningitis, Cryptococcal",D016919,7,3.88E-108
6.65E-112,84,206,Waardenburg Anophthalmia Syndrome,C537769,6,3.88E-108
6.65E-112,84,206,Elliptocytosis 4,C566231,6,3.88E-108
1.08E-111,85,216,THROMBOCYTOPENIA 1 (disorder),C564052,17,6.31E-108
1.77E-111,85,217,Paratuberculosis,D010283,22,1.03E-107
2.74E-111,87,237,Airway Obstruction,D000402,41,1.59E-107
1.85E-111,84,208,"Vasculitis, Leukocytoclastic, Cutaneous",D018366,8,1.08E-107
4.28E-111,87,238,Arterial Occlusive Diseases,D001157,38,2.49E-107
3.07E-111,84,209,Burn injury,D002056,9,1.79E-107
4.67E-111,85,219,Periapical Granuloma,D010484,19,2.72E-107
5.09E-111,84,210,Aspiration Pneumonia,D011015,11,2.96E-107
8.39E-111,84,211,Ovarian Diseases,D010049,18,4.88E-107
1.51E-110,86,231,Bacterial Endocarditis,D004697,34,8.78E-107
3.56E-110,98,372,Alopecia,D000505,197,2.06E-106
4.81E-111,83,201,Heartwater Disease,D006357,1,2.80E-107
8.10E-111,83,202,"Autoimmune Lymphoproliferative Syndrome, Type I, Autosomal Recessive",C566615,2,4.71E-107
8.10E-111,83,202,Follicular cyst,D005497,2,4.71E-107
8.10E-111,83,202,Transitory tachypnea of newborn,D059245,2,4.71E-107
8.10E-111,83,202,"Autoimmune Lymphoproliferative Syndrome, Type IB",C566614,2,4.71E-107
1.36E-110,83,203,"Intestinal Diseases, Parasitic",D007411,5,7.91E-107
2.26E-110,84,213,Cryptosporidiosis,D003457,15,1.31E-106
1.36E-110,83,203,Dermatofibrosis lenticularis disseminata,C537415,4,7.91E-107
1.36E-110,83,203,"Autoimmune Lymphoproliferative Syndrome, Type IA",C566613,3,7.91E-107
5.35E-110,97,360,Trisomy,D014314,178,3.10E-106
2.28E-110,83,204,Histiocytic Necrotizing Lymphadenitis,D020042,4,1.32E-106
2.28E-110,83,204,"Severe combined immunodeficiency, atypical",C537590,4,1.32E-106
5.05E-110,85,224,Stomach Diseases,D013272,26,2.93E-106
6.03E-110,84,215,Latent Tuberculosis,D055985,18,3.50E-106
8.05E-110,85,225,Ocular Hypertension,D009798,34,4.67E-106
6.32E-110,83,206,Invasive Candidiasis,D058365,7,3.67E-106
9.79E-110,84,216,Pelizaeus-Merzbacher Disease,D020371,22,5.68E-106
6.32E-110,83,206,Bronchial Diseases,D001982,6,3.67E-106
6.32E-110,83,206,Macular Holes,D012167,6,3.67E-106
1.42E-109,87,246,High-Grade Squamous Intraepithelial Lesions,D065310,55,8.22E-106
1.44E-109,86,236,Myocardial Reperfusion Injury,D015428,37,8.36E-106
2.92E-109,114,643,Retinoblastoma,D012175,472,1.69E-105
1.05E-109,83,207,Dyggve-Melchior-Clausen syndrome,C535726,8,6.07E-106
1.05E-109,83,207,Carbamoyl-Phosphate Synthase I Deficiency Disease,D020165,8,6.07E-106
2.03E-109,85,227,Arteriovenous fistula,D001164,27,1.18E-105
3.18E-109,89,269,Chronic granulomatous disease,D006105,73,1.84E-105
1.73E-109,83,208,IgG Deficiency disorder,D017099,8,1.00E-105
4.24E-109,88,259,Intestinal Diseases,D007410,68,2.45E-105
2.85E-109,83,209,Complex Regional Pain Syndromes,D020918,11,1.65E-105
2.85E-109,83,209,orbit (eye disorders),D009916,10,1.65E-105
2.85E-109,83,209,Berylliosis,D001607,9,1.65E-105
2.85E-109,83,209,Intestinal Perforation,D007416,9,1.65E-105
2.85E-109,83,209,Pigmented villonodular synovitis,D013586,9,1.65E-105
2.85E-109,83,209,Gangrene,D005734,9,1.65E-105
5.08E-109,87,249,Adenomatous Polyps,D018256,58,2.94E-105
5.09E-109,85,229,Salivary Gland Pleomorphic Adenoma,C563250,31,2.94E-105
9.14E-109,93,318,Neurilemmoma,D009442,125,5.28E-105
6.63E-109,84,220,Pulmonary Sclerosing Hemangioma,D047868,23,3.83E-105
6.63E-109,84,220,"Tuberculosis, Meningeal",D014390,22,3.83E-105
1.48E-108,97,371,Melanocytic nevus,D009508,186,8.52E-105
7.66E-109,83,211,Coxsackievirus Infections,D003384,14,4.43E-105
1.51E-108,89,273,Nevus,D009506,81,8.73E-105
1.25E-108,83,212,Erythema Multiforme,D004892,13,7.22E-105
1.70E-108,84,222,Agranulocytosis,D000380,25,9.79E-105
1.97E-108,85,232,Streptococcal pneumonia,D011018,35,1.14E-104
3.61E-108,119,760,Kidney Diseases,D007674,587,2.08E-104
4.63E-109,82,201,Pityriasis Lichenoides et Varioliformis Acuta,D017514,1,2.68E-105
7.74E-109,82,202,"Neutropenia, Severe Congenital, Autosomal Recessive 4",C567260,2,4.47E-105
7.74E-109,82,202,Dursun Syndrome,C567804,2,4.47E-105
3.27E-108,89,275,Actinic keratosis,D055623,81,1.88E-104
2.03E-108,83,213,Diverticulitis,D004238,14,1.17E-104
1.29E-108,82,203,Multifocal choroiditis,C537374,3,7.43E-105
1.29E-108,82,203,"Neutropenia, Severe Congenital, Autosomal Dominant 1",C565969,3,7.43E-105
4.35E-108,90,287,Gastric ulcer,D013276,91,2.50E-104
2.14E-108,82,204,Trichinellosis,D014235,4,1.23E-104
3.54E-108,82,205,Radicular Cyst,D011842,7,2.04E-104
3.54E-108,82,205,Dysgammaglobulinemia,D004406,6,2.04E-104
1.03E-107,89,278,Steroid Sulfatase Deficiency Disease,D016114,84,5.90E-104
8.61E-108,83,216,"Arthritis, Gouty",D015210,20,4.95E-104
5.84E-108,82,206,Boutonneuse Fever,D001907,6,3.36E-104
5.84E-108,82,206,Uterine Diseases,D014591,6,3.36E-104
1.08E-107,84,226,Costello syndrome (disorder),D056685,28,6.19E-104
9.60E-108,82,207,Rickettsia Infections,D012282,8,5.52E-104
9.60E-108,82,207,Vulvar Vestibulitis,D054515,7,5.52E-104
1.80E-107,85,237,Colonic Polyps,D003111,43,1.03E-103
1.38E-107,83,217,Inflammatory disease of mucous membrane,D052016,17,7.96E-104
2.70E-107,90,292,Vesicular Stomatitis,D054243,119,1.55E-103
2.88E-107,92,316,Malignant neoplasm of testis,D013736,150,1.65E-103
2.95E-107,91,304,Pancytopenia,D010198,109,1.69E-103
2.22E-107,83,218,Mumps,D009107,22,1.27E-103
1.57E-107,82,208,"Tuberculosis, Spinal",D014399,8,9.05E-104
1.57E-107,82,208,Splenic Hypoplasia,C563028,8,9.05E-104
2.57E-107,82,209,Cardiopulmonary Arrest,D006323,12,1.48E-103
2.57E-107,82,209,Onchocerciasis,D009855,11,1.48E-103
3.55E-107,83,219,Corneal Diseases,D003316,26,2.04E-103
3.55E-107,83,219,Coronary Aneurysm,D003323,25,2.04E-103
5.85E-107,86,250,Esophagitis,D004941,60,3.36E-103
5.85E-107,86,250,Intestinal Cancer,D007414,53,3.36E-103
4.19E-107,82,210,Hyperoxia,D018496,10,2.40E-103
4.19E-107,82,210,Amaurosis Fugax,D020757,10,2.40E-103
6.80E-107,82,211,Iridocyclitis,D015863,14,3.90E-103
6.80E-107,82,211,Neuritis,D009443,12,3.90E-103
1.53E-106,87,263,Malignant neoplasm of tongue,D014062,67,8.75E-103
1.53E-106,87,263,Complex Partial Status Epilepticus,D013226,65,8.75E-103
1.10E-106,82,212,Filariasis,D005368,16,6.31E-103
1.10E-106,82,212,Oral Mucositis,D013280,13,6.31E-103
1.43E-106,83,222,Complications of Diabetes Mellitus,D048909,22,8.17E-103
1.43E-106,83,222,"CONSTRICTING BANDS, CONGENITAL",C531614,22,8.17E-103
3.61E-106,121,834,Endometriosis,D004715,672,2.06E-102
2.36E-106,85,243,Gout,D006073,64,1.35E-102
7.18E-107,81,202,"Tuberculosis, Female Genital",D014384,2,4.11E-103
1.78E-106,82,213,Soft Tissue Infections,D018461,14,1.02E-102
3.27E-106,91,311,"Sleep Apnea, Obstructive",D020181,123,1.87E-102
1.19E-106,81,203,Catalase deficiency,D020642,3,6.79E-103
3.60E-106,85,244,"Turner Syndrome, Male",D009634,49,2.06E-102
2.86E-106,82,214,Epidermodysplasia Verruciformis,D004819,19,1.64E-102
2.86E-106,82,214,MERRF Syndrome,D017243,17,1.64E-102
1.95E-106,81,204,"Pyloric Stenosis, Infantile Hypertrophic 1",C566730,5,1.12E-102
3.56E-106,83,224,Sclerosis,D012598,24,2.03E-102
1.95E-106,81,204,HTLV Infections,D006800,4,1.12E-102
1.95E-106,81,204,"Chromosome 8, monosomy 8p",C537825,4,1.12E-102
7.62E-106,100,437,Anaplasia,D000708,255,4.35E-102
4.59E-106,82,215,Gardner Syndrome,D005736,22,2.62E-102
5.60E-106,83,225,Bone Marrow Diseases,D001855,34,3.20E-102
7.86E-106,92,326,Aneurysm,D000783,137,4.49E-102
8.79E-106,83,226,Seborrheic keratosis,D017492,26,5.01E-102
8.55E-106,81,207,Congenital laryngeal adductor palsy,C562861,10,4.88E-102
8.55E-106,81,207,Retinal Drusen,D015593,8,4.88E-102
8.55E-106,81,207,"Ectodermal dysplasia, hypohidrotic, with immune deficiency",C536181,8,4.88E-102
1.38E-105,83,227,Prostatic Hypertrophy,D011470,27,7.85E-102
1.39E-105,81,208,Lymphoid interstitial pneumonia,C562489,10,7.93E-102
1.39E-105,81,208,Experimental Autoimmune Encephalomyelitis,D004681,8,7.93E-102
2.15E-105,83,228,Opportunistic Infections,D009894,28,1.22E-101
2.86E-105,85,249,Glucocorticoid Receptor Deficiency,C564221,50,1.63E-101
3.34E-105,83,229,Ichthyosis linearis circumflexa,D056770,31,1.91E-101
2.96E-105,82,219,Varicocele,D014646,20,1.69E-101
6.73E-105,113,678,Diabetic Nephropathy,D003928,510,3.83E-101
4.69E-105,82,220,"Lipomatosis, Multiple",D008067,25,2.67E-101
6.47E-105,85,251,Multiple Chronic Conditions,D000071069,58,3.68E-101
9.10E-105,88,285,"Leukoencephalopathy, Progressive Multifocal",D007968,94,5.18E-101
1.04E-104,87,274,Lymphadenopathy,D000072281,82,5.94E-101
5.87E-105,81,211,"Radiation Injuries, Experimental",D011833,11,3.34E-101
1.17E-104,82,222,Triploidy syndrome,D057885,37,6.63E-101
1.17E-104,82,222,"Lung Diseases, Obstructive",D008173,25,6.63E-101
1.17E-104,82,222,Hepatic Veno-Occlusive Disease,D006504,23,6.63E-101
2.53E-104,93,350,Neoplasm Invasiveness,D009361,159,1.44E-100
2.74E-104,97,406,Diabetic Retinopathy,D003930,226,1.56E-100
1.51E-104,81,213,Poisoning,D011041,15,8.59E-101
1.83E-104,82,223,Deficiency of glucose-6-phosphate dehydrogenase,D005955,27,1.04E-100
6.47E-105,80,202,Marasmus,D011502,2,3.68E-101
6.47E-105,80,202,"Intracranial Arteriovenous Malformation, Ruptured",D002538,2,3.68E-101
6.47E-105,80,202,Intravenous Drug Abuse,D015819,2,3.68E-101
3.18E-104,87,277,Intervertebral Disc Degeneration,D055959,87,1.81E-100
1.06E-104,80,203,"HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2",C537250,3,6.03E-101
3.22E-104,85,255,Brain Infarction,D020520,59,1.83E-100
2.87E-104,82,224,Dermatitis Herpetiformis,D003874,24,1.63E-100
4.79E-104,85,256,Thyroid Nodule,D016606,58,2.72E-100
4.54E-104,83,235,Microcalcification,D002114,39,2.58E-100
6.10E-104,84,246,SVEINSSON CHORIORETINAL ATROPHY,C566236,50,3.46E-100
2.82E-104,80,205,Bronchopulmonary Sequestration,D001998,5,1.60E-100
7.11E-104,85,257,Ovarian Cysts,D010048,68,4.03E-100
7.28E-104,86,268,Acromegaly,D000172,74,4.13E-100
8.95E-104,92,341,Bone Diseases,D001847,153,5.07E-100
6.98E-104,82,226,Papillary adenoma,D000236,30,3.96E-100
4.57E-104,80,206,Myocardial rupture,D006341,6,2.60E-100
7.40E-104,80,207,Lymphangioma,D008202,8,4.20E-100
1.99E-103,90,318,Ureteral obstruction,D014517,126,1.13E-99
1.68E-103,82,228,"Prostate Cancer, Hereditary, 7",C565201,32,9.53E-100
1.68E-103,82,228,Lichen Sclerosus et Atrophicus,D018459,31,9.53E-100
1.68E-103,82,228,Iron deficiency anemia,D018798,31,9.53E-100
1.53E-103,81,218,Esophageal Achalasia,D004931,20,8.66E-100
1.19E-103,80,208,Megalencephaly cutis marmorata telangiectatica congenita,C536142,8,6.77E-100
2.41E-103,81,219,Camurati-Engelmann Syndrome,C538411,22,1.36E-99
2.41E-103,81,219,Adrenal Cancer,D000310,19,1.36E-99
1.92E-103,80,209,"Pancreatitis, Acute Necrotizing",D019283,9,1.09E-99
3.74E-103,83,240,Diabetic Foot,D017719,41,2.11E-99
5.69E-103,91,334,Weight decreased,D015431,152,3.22E-99
3.08E-103,80,210,Fibromatosis,D005350,13,1.74E-99
3.08E-103,80,210,Lymphatic Abnormalities,D044148,11,1.74E-99
3.08E-103,80,210,Infarction,D007238,10,1.74E-99
6.87E-103,84,252,Rheumatic Fever,D012213,55,3.88E-99
6.18E-103,82,231,Sickle Cell Trait,D012805,36,3.49E-99
7.30E-103,85,263,"Liver Cirrhosis, Alcoholic",D008104,68,4.12E-99
4.92E-103,80,211,Dermoid Cyst,D003884,14,2.78E-99
5.93E-103,81,221,"Creutzfeldt-Jakob Disease, Sporadic",C565143,25,3.35E-99
8.83E-103,88,298,Peripheral Arterial Diseases,D058729,118,4.98E-99
8.83E-103,88,298,Von Hippel-Lindau Syndrome,D006623,105,4.98E-99
4.92E-103,80,211,Pharyngitis,D010612,11,2.78E-99
9.93E-103,86,275,Otitis Media,D010033,91,5.60E-99
9.49E-103,82,232,Rheumatic Heart Disease,D012214,36,5.36E-99
1.29E-102,83,243,Muscular Atrophy,D009133,46,7.28E-99
1.56E-102,85,265,"Cicatrix, Hypertrophic",D017439,72,8.81E-99
1.25E-102,80,213,Laryngeal cleft,C537875,16,7.04E-99
2.63E-102,95,394,Hyperlipidemia,D006949,204,1.48E-98
1.94E-102,83,244,Hepatocellular Adenoma,D018248,47,1.09E-98
5.66E-103,79,202,Radiation Syndrome,D011832,2,3.20E-99
2.22E-102,82,234,"Neoplasm Recurrence, Local",D009364,35,1.25E-98
3.39E-102,87,290,Neoplastic Cell Transformation,D002471,94,1.91E-98
3.32E-102,85,267,Pulmonary Edema,D011654,73,1.87E-98
3.39E-102,82,235,Alcoholic Steatohepatitis,D005235,37,1.91E-98
5.73E-102,105,560,Vascular Diseases,D014652,373,3.22E-98
3.13E-102,80,215,Coronary Restenosis,D023903,16,1.76E-98
5.99E-102,89,316,Nerve Degeneration,D009410,138,3.37E-98
4.93E-102,80,216,Congenital hernia of foramen of Bochdalek,D065630,17,2.78E-98
3.88E-102,79,206,"Chromosome 12, 12p trisomy",C538299,7,2.18E-98
3.88E-102,79,206,Angiodysplasia,D016888,6,2.18E-98
9.58E-102,87,293,Teratoma,D013724,104,5.39E-98
1.17E-101,98,445,Cerebral Infarction,D002544,261,6.58E-98
7.76E-102,80,217,Type II Mucolipidosis,D009081,23,4.37E-98
7.76E-102,80,217,Myoma,D009214,17,4.37E-98
1.47E-101,94,386,"Hepatitis, Drug-Induced",D056486,203,8.27E-98
1.19E-101,82,238,Hematuria,D006417,46,6.67E-98
1.19E-101,82,238,Fibromyalgia,D005356,46,6.67E-98
1.19E-101,82,238,gallbladder neoplasm,D005706,39,6.67E-98
1.28E-101,81,228,Hepatic Encephalopathy,D006501,35,7.21E-98
1.22E-101,80,218,Menkes Kinky Hair Syndrome,D007706,23,6.84E-98
1.22E-101,80,218,Bloch Sulzberger syndrome,D007184,20,6.84E-98
9.96E-102,79,208,Arthus Reaction,D001183,8,5.60E-98
9.96E-102,79,208,"Cardiomyopathy, Alcoholic",D002310,8,5.60E-98
2.53E-101,88,308,Malignant neoplasm of larynx,D007822,111,1.42E-97
1.97E-101,81,229,Gastrinoma,D015408,29,1.11E-97
1.90E-101,80,219,Cyclic neutropenia,C536227,22,1.07E-97
3.02E-101,81,230,Chikungunya Fever,D065632,38,1.69E-97
2.97E-101,80,220,Pericardial effusion,D010490,25,1.67E-97
2.53E-101,79,210,"Hydatidiform Mole, Partial",D006828,13,1.42E-97
4.88E-101,88,310,Streptozotocin Diabetes,D003921,110,2.73E-97
4.01E-101,79,211,Manganese Poisoning,D020149,12,2.25E-97
7.04E-101,81,232,Vitamin D Deficiency,D014808,35,3.95E-97
9.10E-101,85,276,Diabetic Neuropathies,D003929,78,5.09E-97
7.17E-101,80,222,African Trypanosomiasis,D014353,29,4.02E-97
7.17E-101,80,222,"Encephalopathy, Toxic",D020258,25,4.02E-97
6.35E-101,79,212,Codependency,D017004,14,3.56E-97
1.11E-100,80,223,Collagen Diseases,D003095,26,6.21E-97
1.37E-100,82,244,Atypical Ductal Breast Hyperplasia,D002285,46,7.66E-97
1.00E-100,79,213,"Heart Failure, Diastolic",D054144,14,5.61E-97
1.52E-100,83,255,Proliferative vitreoretinopathy,D018630,59,8.51E-97
4.81E-101,78,202,Hypertensive Encephalopathy,D020343,2,2.70E-97
4.81E-101,78,202,Cardiac Tamponade,D002305,2,2.70E-97
7.76E-101,78,203,Chilblain lupus 1,C535924,4,4.35E-97
7.76E-101,78,203,Ocular Hypotension,D015814,4,4.35E-97
7.76E-101,78,203,Hyperzincemia and Hypercalprotectinemia,C565988,3,4.35E-97
1.58E-100,79,214,Sacroiliitis,D058566,14,8.82E-97
3.64E-100,94,398,"Anemia, Sickle Cell",D000755,213,2.04E-96
1.25E-100,78,204,"Osteoarthropathy, Primary Hypertrophic",D010004,5,6.98E-97
1.25E-100,78,204,Urinary Schistosomiasis,D012553,4,6.98E-97
2.64E-100,80,225,Angiomyolipoma,D018207,29,1.48E-96
3.04E-100,82,246,Coronary Stenosis,D023921,47,1.70E-96
2.64E-100,80,225,Craniopharyngioma,D003397,25,1.48E-96
5.19E-100,101,511,Age related macular degeneration,D008268,348,2.90E-96
5.73E-100,92,371,Craniosynostosis,D003398,198,3.19E-96
4.06E-100,80,226,Pyelonephritis,D011704,35,2.27E-96
3.87E-100,79,216,Dysgerminoma,D004407,25,2.16E-96
3.87E-100,79,216,Aniridia,D015783,20,2.16E-96
3.87E-100,79,216,Coronary Artery Vasospasm,D003329,19,2.16E-96
6.22E-100,80,227,Acanthosis Nigricans,D000052,31,3.47E-96
6.22E-100,80,227,Central Diabetes Insipidus,D020790,30,3.47E-96
5.09E-100,78,207,Specific granule deficiency,C562873,8,2.84E-96
5.09E-100,78,207,Myofibromatosis,D018224,7,2.84E-96
5.09E-100,78,207,Glycogen Storage Disease Type VI,D006013,7,2.84E-96
9.94E-100,82,249,"Inclusion Body Myopathy, Sporadic",D018979,56,5.53E-96
9.52E-100,80,228,Aortic valve calcification,C562942,29,5.30E-96
9.42E-100,79,218,Traumatic injury,D014947,18,5.25E-96
8.08E-100,78,208,Hepatopulmonary Syndrome,D020065,8,4.50E-96
8.08E-100,78,208,Hemoptysis,D006469,8,4.50E-96
1.45E-99,80,229,"Albinism, Oculocutaneous",D016115,30,8.09E-96
3.05E-99,89,336,Turner Syndrome,D014424,144,1.70E-95
2.21E-99,80,230,"Purpura, Thrombotic Thrombocytopenic",D011697,35,1.23E-95
2.21E-99,80,230,"Arthritis, Reactive",D016918,33,1.23E-95
2.02E-99,78,210,hemangiopericytoma,D006393,11,1.13E-95
2.02E-99,78,210,HIV-Associated Lipodystrophy Syndrome,D039682,10,1.13E-95
2.02E-99,78,210,Pulmonary Blastoma,D018202,10,1.13E-95
3.50E-99,79,221,Multi-infarct dementia,D015161,21,1.94E-95
4.68E-99,82,253,"AURAL ATRESIA, CONGENITAL",C564321,57,2.60E-95
3.18E-99,78,211,"Gaucher Disease, Type 3 (disorder)",D005776,14,1.77E-95
5.09E-99,80,232,Pseudoxanthoma Elasticum,D011561,34,2.82E-95
5.09E-99,80,232,Escherichia coli Infections,D004927,34,2.82E-95
5.09E-99,80,232,Paranoid Schizophrenia,D012563,32,2.82E-95
5.39E-99,79,222,Pemphigus,D010392,30,2.99E-95
6.86E-99,82,254,Dry Eye Syndromes,D015352,57,3.80E-95
5.00E-99,78,212,Paraneoplastic Syndromes,D010257,14,2.78E-95
7.69E-99,80,233,"Hyperparathyroidism, Secondary",D006962,35,4.26E-95
9.41E-99,81,244,Friedreich Ataxia,D005621,49,5.21E-95
9.41E-99,81,244,Breast Diseases,D001941,45,5.21E-95
8.29E-99,79,223,Leg Ulcer,D007871,25,4.60E-95
8.29E-99,79,223,"Microangiopathy, Diabetic",D003925,23,4.60E-95
1.21E-98,85,290,Lipodystrophy,D008060,101,6.72E-95
2.48E-99,77,201,"Charcot-Marie-Tooth disease, axonal, Type 2G",C539595,1,1.38E-95
2.48E-99,77,201,Jankovic Rivera syndrome,C537563,1,1.38E-95
2.48E-99,77,201,Mercurial Neuroanesthenia,D020262,1,1.38E-95
2.48E-99,77,201,Presentey Anomaly,C564893,1,1.38E-95
2.48E-99,77,201,"Thyrotropin-Releasing Hormone Resistance, Generalized",C566049,1,1.38E-95
3.98E-99,77,202,Community-Acquired Infections,D017714,2,2.21E-95
6.36E-99,77,203,MASP2 Deficiency,C565360,3,3.53E-95
6.36E-99,77,203,Complement Factor I (C3 inactivator) deficiency,C572568,3,3.53E-95
6.36E-99,77,203,Malpuech facial clefting syndrome,C535704,3,3.53E-95
6.36E-99,77,203,Coccidioidomycosis,D003047,3,3.53E-95
2.07E-98,81,246,Febrile Convulsions,D003294,59,1.14E-94
1.01E-98,77,204,Bile duct adenoma,D002759,5,5.62E-95
3.89E-98,98,480,Impaired glucose tolerance,D018149,300,2.15E-94
2.62E-98,80,236,Strawberry nevus of skin,D018324,39,1.45E-94
1.61E-98,77,205,Malignant neoplasm of appendix,D001063,5,8.93E-95
2.96E-98,78,216,Chromosome 11p11.2 Deletion Syndrome,C538356,21,1.64E-94
2.96E-98,78,216,Nodular Goiter,D006044,18,1.64E-94
4.50E-98,81,248,Heart valve disease,D006349,53,2.49E-94
2.56E-98,77,206,Myelolipoma,D018209,6,1.41E-94
2.56E-98,77,206,Hepatorenal Syndrome,D006530,6,1.41E-94
2.56E-98,77,206,Aseptic Meningitis,D008582,6,1.41E-94
6.56E-98,82,260,Paroxysmal kinesigenic choreoathetosis,C537180,71,3.62E-94
5.88E-98,80,238,Endometriosis of uterus,D062788,42,3.25E-94
6.62E-98,81,249,Sinusitis,D012852,52,3.66E-94
6.62E-98,81,249,Progeria,D011371,51,3.66E-94
4.04E-98,77,207,Postherpetic neuralgia,D051474,10,2.23E-94
8.28E-98,83,272,Cardiac Hypertrophy,D006332,74,4.57E-94
1.45E-97,105,613,Congenital chromosomal disease,D025063,440,8.02E-94
7.09E-98,78,218,Fleck corneal dystrophy,C563256,18,3.91E-94
1.04E-97,79,229,Keratosis,D007642,35,5.74E-94
1.86E-97,91,378,Pulmonary Emphysema,D011656,194,1.03E-93
1.00E-97,77,209,"Angina Pectoris, Variant",D000788,11,5.52E-94
1.00E-97,77,209,"Nevus, Blue",D018329,10,5.52E-94
1.00E-97,77,209,Musculoskeletal Diseases,D009140,10,5.52E-94
1.00E-97,77,209,"Scleroderma, Limited",D045745,10,5.52E-94
1.57E-97,79,230,Lymphatic Diseases,D008206,34,8.67E-94
1.57E-97,77,210,ALZHEIMER DISEASE 5,C566578,12,8.65E-94
2.37E-97,79,231,Disease due to Parvoviridae,D010322,37,1.31E-93
2.88E-97,80,242,Leukocyte adhesion deficiency type 1,C535887,44,1.59E-93
7.32E-97,86,315,Reticulocyte count (procedure),D017701,167,4.02E-93
6.46E-97,81,255,Hereditary pancreatitis,C537262,59,3.55E-93
9.98E-97,97,478,Diarrhea,D003967,302,5.48E-93
6.02E-97,78,223,Elastosis perforans serpiginosa,C536202,23,3.31E-93
6.02E-97,78,223,Acute Lung Injury,D055371,23,3.31E-93
5.94E-97,77,213,Reoviridae Infections,D012088,15,3.27E-93
8.04E-97,79,234,Japanese Encephalitis,D004672,38,4.41E-93
3.19E-97,76,202,Hereditary Angioedema Type I,D056829,2,1.76E-93
3.19E-97,76,202,Transient hypertension of pregnancy,D046110,2,1.76E-93
3.19E-97,76,202,Hepatic venoocclusive disease with immunodeficiency,C537257,2,1.76E-93
3.19E-97,76,202,Metaphyseal anadysplasia,C537351,2,1.76E-93
3.19E-97,76,202,Oculopalatoskeletal syndrome,C537738,2,1.76E-93
3.19E-97,76,202,Carnevale syndrome,C535586,2,1.76E-93
1.64E-96,88,344,Keloid,D007627,160,8.97E-93
1.20E-96,79,235,Transient Cerebral Ischemia,D002546,40,6.60E-93
5.07E-97,76,203,Complement Factor H Deficiency,C562875,3,2.79E-93
5.07E-97,76,203,Pyoderma,D011711,3,2.79E-93
5.07E-97,76,203,Communication impairment,D003147,3,2.79E-93
2.55E-96,103,590,Osteoporosis,D010024,410,1.39E-92
8.01E-97,76,204,Dianzani autoimmune lymphoproliferative syndrome,C535950,5,4.40E-93
8.01E-97,76,204,Postpartum Thyroiditis,D050032,5,4.40E-93
8.01E-97,76,204,Patau syndrome,D000073839,5,4.40E-93
2.73E-96,99,517,Ataxia Telangiectasia,D001260,340,1.49E-92
2.00E-96,80,247,"ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 1",C565062,58,1.10E-92
8.01E-97,76,204,Nelson Syndrome,D009347,4,4.40E-93
8.01E-97,76,204,Rheumatoid Vasculitis,D056653,4,4.40E-93
8.01E-97,76,204,Fetal Hypoxia,D005311,4,4.40E-93
8.01E-97,76,204,Trisomy 22,C536799,4,4.40E-93
1.42E-96,77,215,Morphine Dependence,D009021,15,7.81E-93
2.11E-96,78,226,Albuminuria,D000419,27,1.16E-92
2.20E-96,77,216,Carpal Tunnel Syndrome,D002349,24,1.20E-92
3.42E-96,86,320,Hypertriglyceridemia,D015228,139,1.87E-92
1.26E-96,76,205,Bursitis,D002062,5,6.93E-93
2.94E-96,80,248,"Respiratory Distress Syndrome, Newborn",D012127,52,1.61E-92
3.50E-96,82,271,Pregnancy Complications,D011248,82,1.91E-92
3.50E-96,82,271,Peptic Ulcer,D010437,75,1.91E-92
3.19E-96,78,227,Refractory anaemia with excess blasts,D000754,29,1.75E-92
1.99E-96,76,206,Glycogen storage disease type Ia,C538655,7,1.09E-92
1.99E-96,76,206,Sinus histiocytosis,D015618,7,1.09E-92
4.10E-96,81,260,"Niemann-Pick Disease, Type C",D052556,66,2.24E-92
3.38E-96,77,217,"Signs and Symptoms, Respiratory",D012818,22,1.85E-92
3.38E-96,77,217,Adenosis of Breast,D005348,19,1.85E-92
7.35E-96,91,392,Pituitary Diseases,D010900,216,4.01E-92
4.82E-96,78,228,"Stickler syndrome, type 1",C537492,32,2.63E-92
7.02E-96,84,297,Polycystic Kidney Diseases,D007690,110,3.83E-92
3.12E-96,76,207,Post-Traumatic Myelopathy,D013119,7,1.71E-92
5.19E-96,77,218,Diabetic Ketoacidosis,D016883,18,2.83E-92
5.19E-96,77,218,Peyronie Disease,D010411,18,2.83E-92
4.88E-96,76,208,Denys-Drash Syndrome,D030321,9,2.66E-92
4.88E-96,76,208,Hyperargininemia,D020162,8,2.66E-92
9.14E-96,80,251,"Bulbo-Spinal Atrophy, X-Linked",D055534,55,4.99E-92
8.71E-96,79,240,Oral Submucous Fibrosis,D009914,41,4.76E-92
7.94E-96,77,219,pathologic fistula,D005402,20,4.33E-92
1.55E-95,86,325,Adrenoleukodystrophy,D000326,136,8.47E-92
1.33E-95,80,252,Atrophic,D001284,53,7.25E-92
1.21E-95,77,220,Cervical dysplasia,D002578,24,6.61E-92
1.63E-95,78,231,Autosomal Recessive Polycystic Kidney Disease,D017044,34,8.89E-92
1.93E-95,80,253,Hyperuricemia,D033461,64,1.05E-91
1.18E-95,76,210,Priapism,D011317,10,6.45E-92
1.85E-95,77,221,Indian childhood cirrhosis,C562580,24,1.01E-91
2.44E-95,78,232,Conjunctivitis,D003231,40,1.33E-91
2.81E-95,77,222,Hepatitis E,D016751,33,1.52E-91
4.04E-95,80,255,Malocclusion,D008310,64,2.19E-91
4.04E-95,80,255,"Leukoplakia, Oral",D007972,62,2.19E-91
2.84E-95,76,212,Active Hyperemia,D006940,12,1.54E-91
5.07E-95,81,267,"Condition, Preneoplastic",D011230,85,2.75E-91
4.26E-95,77,223,Overlap syndrome,D000074079,27,2.31E-91
6.00E-95,79,245,Dentatorubral-Pallidoluysian Atrophy,D020191,54,3.25E-91
2.49E-95,75,202,Vaginal Hemorrhage,D014592,3,1.35E-91
2.49E-95,75,202,Borrelia Infections,D001899,3,1.35E-91
6.44E-95,77,224,"Ventricular Dysfunction, Left",D018487,27,3.48E-91
8.42E-95,80,257,Pterygium,D011625,61,4.56E-91
2.49E-95,75,202,"Panniculitis, Nodular Nonsuppurative",D010201,2,1.35E-91
2.49E-95,75,202,Staphylococcal Pneumonia,D011023,2,1.35E-91
2.49E-95,75,202,Duodenal Diseases,D004378,2,1.35E-91
2.49E-95,75,202,Newcastle Disease,D009521,2,1.35E-91
1.58E-95,75,201,"Ehlers-Danlos Syndrome, Type VIII",C562626,1,8.60E-92
1.58E-95,75,201,"Macular Degeneration, Age-Related, 10",C566935,1,8.60E-92
1.58E-95,75,201,Complement Component C1s Deficiency,C565170,1,8.60E-92
1.58E-95,75,201,Acne Conglobata,D000069316,1,8.60E-92
1.58E-95,75,201,"Complement Component 4, Partial Deficiency Of",C565168,1,8.60E-92
1.58E-95,75,201,Laryngeal Edema,D007819,1,8.60E-92
1.58E-95,75,201,"Granuloma, Foreign-Body",D015745,1,8.60E-92
1.58E-95,75,201,Hemophilus influenza infection,D006192,1,8.60E-92
1.58E-95,75,201,Bordetella Infections,D001885,1,8.60E-92
6.74E-95,76,214,Atypical Endometrial Hyperplasia,D004714,16,3.65E-91
3.92E-95,75,203,Periostitis,D010522,3,2.13E-91
3.92E-95,75,203,RNA Virus Infections,D012327,3,2.13E-91
3.92E-95,75,203,"Bone Demineralization, Pathologic",D018488,3,2.13E-91
3.92E-95,75,203,Light Fixation Seizure Syndrome,C566367,3,2.13E-91
1.70E-94,95,468,Anoxia,D000860,277,9.18E-91
6.15E-95,75,204,Zoonoses,D015047,6,3.33E-91
6.15E-95,75,204,Adamantinoma,D050398,5,3.33E-91
6.15E-95,75,204,Oxalosis,D006959,5,3.33E-91
6.15E-95,75,204,Hyperemesis Gravidarum,D006939,4,3.33E-91
6.15E-95,75,204,Giant Cell Granuloma,D006101,4,3.33E-91
6.15E-95,75,204,Mesoblastic Nephroma,D018201,4,3.33E-91
6.15E-95,75,204,Parapsoriasis en Plaques,D010267,4,3.33E-91
6.15E-95,75,204,Pleuropneumonia,D011001,4,3.33E-91
6.15E-95,75,204,Maffucci Syndrome,D004687,4,3.33E-91
1.46E-94,77,226,Subfertility,D007246,35,7.91E-91
1.46E-94,77,226,Leukoaraiosis,D049292,34,7.91E-91
9.62E-95,75,205,Buruli Ulcer,D054312,7,5.21E-91
1.77E-94,78,237,Right Ventricular Hypertrophy,D017380,43,9.55E-91
9.62E-95,75,205,Chiari malformation type II,D001139,6,5.21E-91
1.59E-94,76,216,Peri-Implantitis,D057873,16,8.57E-91
3.20E-94,91,407,Overweight,D050177,221,1.72E-90
2.20E-94,77,227,Juvenile polyposis syndrome,C537702,27,1.19E-90
1.50E-94,75,206,Spondylitis,D013166,6,8.12E-91
1.50E-94,75,206,Avitaminosis,D001361,6,8.12E-91
1.50E-94,75,206,Felty Syndrome,D005258,6,8.12E-91
2.42E-94,76,217,Cerebral Vasospasm,D020301,19,1.31E-90
2.42E-94,76,217,Saethre-Chotzen Syndrome,D000168,18,1.31E-90
2.34E-94,75,207,Waisman syndrome,C537179,9,1.26E-90
2.34E-94,75,207,Immunoproliferative Small Intestinal Disease,D007161,8,1.26E-90
2.34E-94,75,207,Capillary Leak Syndrome,D019559,8,1.26E-90
2.34E-94,75,207,Treatment related secondary malignancy,D016609,7,1.26E-90
2.34E-94,75,207,Vasogenic Cerebral Edema,D001929,7,1.26E-90
5.70E-94,79,251,Fibroadenoma,D018226,58,3.07E-90
5.66E-94,78,240,Intracranial Hemorrhages,D020300,45,3.05E-90
3.63E-94,75,208,Fowlpox,D005586,10,1.96E-90
3.63E-94,75,208,Leukostasis,D018921,9,1.96E-90
7.34E-94,77,230,Intestinal Polyps,D007417,39,3.95E-90
5.62E-94,75,209,Progesterone Resistance,C564871,11,3.03E-90
5.62E-94,75,209,Poliomyelitis,D011051,10,3.03E-90
5.62E-94,75,209,Rotator cuff syndrome,D000070636,10,3.03E-90
5.62E-94,75,209,Anterior myocardial infarction,D056988,9,3.03E-90
5.62E-94,75,209,"Tuberculosis, Central Nervous System",D020306,9,3.03E-90
8.50E-94,76,220,Smith-Magenis syndrome,D058496,26,4.58E-90
1.09E-93,77,231,Blood Platelet Disorders,D001791,34,5.88E-90
1.22E-93,78,242,"Hypertension, Renovascular",D006978,44,6.54E-90
8.67E-94,75,210,Eosinophilia-Myalgia Syndrome,D016603,10,4.66E-90
1.62E-93,77,232,"CATARACT, ANTERIOR POLAR",C538282,38,8.72E-90
1.34E-93,75,211,Cholera Infantum,D005767,12,7.17E-90
1.34E-93,75,211,Heterochromia iridis,C538115,11,7.17E-90
1.34E-93,75,211,"Cerebral Amyloid Angiopathy, Hereditary",D028243,11,7.17E-90
1.34E-93,75,211,Childhood Ependymoma,C531673,11,7.17E-90
1.94E-93,76,222,PEELING SKIN SYNDROME,C564818,28,1.04E-89
2.47E-93,79,255,Multiple Endocrine Neoplasia Type 2a,D018813,55,1.32E-89
2.98E-93,82,291,"Obesity, Morbid",D009767,103,1.59E-89
2.05E-93,75,212,Intestinal Volvulus,D045822,16,1.10E-89
2.05E-93,75,212,Cherubism,D002636,13,1.10E-89
2.92E-93,76,223,Keratosis Follicularis,D007644,25,1.57E-89
3.14E-93,75,213,Meconium Aspiration Syndrome,D008471,16,1.68E-89
3.14E-93,75,213,Malignant neoplasm tonsil,D014067,14,1.68E-89
1.88E-93,74,202,Blood Sedimentation,D001799,4,1.01E-89
3.14E-93,75,213,Urinary Bladder Diseases,D001745,13,1.68E-89
3.14E-93,75,213,Cystathionine beta-Synthase Deficiency Disease,D006712,13,1.68E-89
4.39E-93,76,224,Angiofibroma,D018322,26,2.35E-89
1.88E-93,74,202,Claustrophobia,D010698,3,1.01E-89
5.94E-93,80,269,Insulin Resistance,D007333,71,3.17E-89
9.37E-93,109,765,Amyotrophic Lateral Sclerosis,D000690,606,4.99E-89
7.92E-93,88,375,Left Ventricular Hypertrophy,D017379,183,4.22E-89
9.42E-93,96,504,Nephroblastoma,D009396,320,5.02E-89
7.81E-93,82,294,Hereditary Nonpolyposis Colorectal Cancer,D003123,108,4.16E-89
1.88E-93,74,202,Persistent Vegetative State,D018458,2,1.01E-89
1.88E-93,74,202,"Crossed Polydactyly, Type I",C566783,2,1.01E-89
1.88E-93,74,202,Intracranial Arteriosclerosis,D002537,2,1.01E-89
1.88E-93,74,202,Singleton Merten syndrome,C537343,2,1.01E-89
1.88E-93,74,202,Cerebrovascular Insufficiency,D002561,2,1.01E-89
1.88E-93,74,202,NAVAJO NEUROHEPATOPATHY,C538344,2,1.01E-89
1.20E-93,74,201,"Infant, Very Low Birth Weight",D019102,1,6.47E-90
1.20E-93,74,201,Nodular Elastoidosis,D005148,1,6.47E-90
1.20E-93,74,201,"Macular Degeneration, Age-Related, 9",C566958,1,6.47E-90
1.20E-93,74,201,"COMPLEMENT COMPONENT 3 DEFICIENCY, AUTOSOMAL RECESSIVE",C565169,1,6.47E-90
1.20E-93,74,201,C9 Deficiency,C565165,1,6.47E-90
1.20E-93,74,201,Annular Erythema,C562461,1,6.47E-90
2.94E-93,74,203,DOYNE HONEYCOMB RETINAL DYSTROPHY,C535602,4,1.58E-89
7.97E-93,78,247,"Subfertility, Male",D007248,56,4.25E-89
2.94E-93,74,203,Retinal Artery Occlusion,D015356,3,1.58E-89
2.94E-93,74,203,"Drusen, Radial, Autosomal Dominant",C565088,3,1.58E-89
4.58E-93,74,204,Trichiasis,D058457,5,2.45E-89
4.58E-93,74,204,Hereditary Sensory and Autonomic Neuropathy Type Ie,C580162,4,2.45E-89
4.58E-93,74,204,Nutrition Disorders,D009748,4,2.45E-89
4.58E-93,74,204,Duodenitis,D004382,4,2.45E-89
4.58E-93,74,204,Adnexal Diseases,D000291,4,2.45E-89
4.58E-93,74,204,Hemoglobin SC Disease,D006450,4,2.45E-89
7.12E-93,74,205,Isovaleryl-CoA dehydrogenase deficiency,C538167,7,3.80E-89
1.11E-92,75,216,Bare lymphocyte syndrome 2,C537079,21,5.92E-89
7.12E-93,74,205,Myelitis,D009187,6,3.80E-89
7.12E-93,74,205,"PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS",C564461,5,3.80E-89
7.12E-93,74,205,Tension Headache,D018781,5,3.80E-89
7.12E-93,74,205,Malignant neoplasm of cecum,D002430,5,3.80E-89
7.12E-93,74,205,Spinal Cord Ischemia,D020760,5,3.80E-89
7.12E-93,74,205,Sunburn,D013471,5,3.80E-89
7.12E-93,74,205,CD59 Deficiency,C567355,5,3.80E-89
1.47E-92,76,227,Prostatic Diseases,D011469,32,7.81E-89
1.69E-92,75,217,Adrenal Gland Hyperfunction,D000308,20,8.97E-89
1.10E-92,74,206,Central Neurocytoma,D018306,6,5.87E-89
1.10E-92,74,206,Vascular ring,D000073872,6,5.87E-89
4.07E-92,109,775,Impaired cognition,D060825,613,2.16E-88
3.17E-92,81,286,Sciatic Neuropathy,D020426,90,1.68E-88
1.70E-92,74,207,Erysipelas,D004886,8,9.06E-89
3.79E-92,82,299,Premature Birth,D047928,116,2.01E-88
1.70E-92,74,207,Bone Resorption,D001862,7,9.06E-89
2.55E-92,75,218,Intestinal Pseudo-Obstruction,D007418,21,1.36E-88
2.55E-92,75,218,Infantile neuronal ceroid lipofuscinosis,D009472,19,1.36E-88
3.58E-92,77,240,Purpura,D011693,40,1.90E-88
2.62E-92,74,208,AROMATASE EXCESS SYNDROME,C000591739,9,1.39E-88
2.62E-92,74,208,Pathological Dilatation,D004108,8,1.39E-88
3.85E-92,75,219,Acute Kidney Tubular Necrosis,D007683,19,2.05E-88
6.06E-92,81,288,Hypercalcemia,D006934,93,3.21E-88
6.39E-92,80,276,Acute Confusional Senile Dementia,D000544,81,3.39E-88
4.03E-92,74,209,"Epilepsy, Tonic-Clonic, Symptomatic",D004830,10,2.14E-88
4.03E-92,74,209,Vascular System Injuries,D057772,9,2.14E-88
4.03E-92,74,209,Yersinia infections,D015009,9,2.14E-88
5.80E-92,75,220,Osteophyte,D054850,22,3.08E-88
8.92E-92,80,277,"Dementia, Vascular",D015140,79,4.73E-88
6.18E-92,74,210,"Chromosome 10, monosomy 10q",C538289,11,3.28E-88
1.02E-91,78,254,Retinopathy of Prematurity,D012178,60,5.42E-88
6.18E-92,74,210,"Colitis, Ischemic",D017091,10,3.28E-88
8.71E-92,75,221,"alpha-1-Antitrypsin Deficiency, Autosomal Recessive",C566273,23,4.62E-88
1.33E-91,83,316,Motor Neuron Disease,D016472,127,7.05E-88
1.31E-91,82,303,Lymphatic Metastasis,D008207,113,6.93E-88
8.71E-92,75,221,Retinal Vein Occlusion,D012170,22,4.62E-88
9.44E-92,74,211,"Amyloid Neuropathies, Familial",D028227,12,4.99E-88
9.44E-92,74,211,"Stroke, Lacunar",D059409,12,4.99E-88
2.06E-91,87,373,Myxoid cyst,D045888,195,1.09E-87
1.55E-91,76,233,Ovarian Hyperstimulation Syndrome,D016471,33,8.17E-88
1.44E-91,74,212,Arteriosclerosis Obliterans,D001162,12,7.60E-88
1.44E-91,74,212,Homocysteinemia,C566403,12,7.60E-88
1.44E-91,74,212,Takotsubo Cardiomyopathy,D054549,12,7.60E-88
1.44E-91,74,212,Viral meningitis,D008587,12,7.60E-88
2.28E-91,76,234,"AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED",C567782,41,1.20E-87
4.13E-91,95,505,Retinal Diseases,D012164,328,2.17E-87
2.19E-91,74,213,Congenital heart block,C535758,15,1.15E-87
2.19E-91,74,213,Focal Nodular Hyperplasia,D020518,15,1.15E-87
4.07E-91,85,347,Prostatic Intraepithelial Neoplasias,D019048,165,2.14E-87
2.19E-91,74,213,Copper-Overload Cirrhosis,C566858,13,1.15E-87
2.19E-91,74,213,"Peroxisome Biogenesis Disorder, Complementation Group D",C566388,13,1.15E-87
2.91E-91,75,224,ST segment elevation myocardial infarction,D000072657,26,1.53E-87
3.34E-91,76,235,"Depression, Neurotic",D003866,38,1.76E-87
1.39E-91,73,202,"Myopathy, Actin, Congenital, with Excess of Thin Myofilaments",C563529,3,7.32E-88
1.39E-91,73,202,Chudley-Mccullough syndrome,C535459,3,7.32E-88
3.32E-91,74,214,Congenital bilateral aplasia of vas deferens,C535984,17,1.75E-87
3.32E-91,74,214,"Histiocytoma, Benign Fibrous",D018219,17,1.75E-87
3.32E-91,74,214,Non-ST Elevated Myocardial Infarction,D000072658,15,1.75E-87
3.32E-91,74,214,BREAST CANCER 3,C565336,14,1.75E-87
4.34E-91,75,225,"Nephritis, Tubulointerstitial",D009395,33,2.28E-87
1.39E-91,73,202,"Chromosome 6, monosomy 6q",C537807,2,7.32E-88
1.39E-91,73,202,"T-Lymphocytopenia, Idiopathic CD4-Positive",D018344,2,7.32E-88
8.92E-92,73,201,"Polyglandular Deficiency Syndrome, Persian-Jewish Type",C538275,1,4.73E-88
8.92E-92,73,201,Baller-Gerold syndrome,C536788,1,4.73E-88
8.92E-92,73,201,"Macular Degeneration, Age-Related, 7",C565718,1,4.73E-88
8.92E-92,73,201,Oral Manifestations,D009912,1,4.73E-88
8.92E-92,73,201,Tenosynovitis,D013717,1,4.73E-88
8.92E-92,73,201,"MACULAR DEGENERATION, AGE-RELATED, 4 (disorder)",C565196,1,4.73E-88
8.92E-92,73,201,Bovine Anaplasmosis,D000712,1,4.73E-88
8.92E-92,73,201,Diverticulum,D004240,1,4.73E-88
4.34E-91,75,225,Intestinal Obstruction,D007415,27,2.28E-87
2.15E-91,73,203,Atheroma,D058226,3,1.13E-87
2.15E-91,73,203,"Shock, Cardiogenic",D012770,3,1.13E-87
2.15E-91,73,203,Conus Medullaris Syndrome,D013117,3,1.13E-87
2.15E-91,73,203,Prurigo,D011536,3,1.13E-87
6.95E-91,77,248,NONAKA MYOPATHY,C536816,50,3.65E-87
5.02E-91,74,215,Bone Cysts,D001845,16,2.64E-87
6.44E-91,75,226,Tendinopathy,D052256,28,3.38E-87
6.44E-91,75,226,Renal hypertension,D006977,28,3.38E-87
3.32E-91,73,204,Periapical Diseases,D010483,4,1.75E-87
3.32E-91,73,204,Granuloma Annulare,D016460,4,1.75E-87
3.32E-91,73,204,Nephrogenic Syndrome of Inappropriate Antidiuresis,C564491,4,1.75E-87
5.12E-91,73,205,Langer-Giedion Syndrome,D015826,7,2.69E-87
7.59E-91,74,216,ANOPHTHALMIA AND PULMONARY HYPOPLASIA,C537768,18,3.98E-87
7.59E-91,74,216,Cerebral Small Vessel Diseases,D059345,17,3.98E-87
5.12E-91,73,205,"Ophthalmia, Sympathetic",D009879,6,2.69E-87
1.04E-90,76,238,Cardiovascular Abnormalities,D018376,45,5.46E-87
5.12E-91,73,205,Trichomonas Infections,D014245,5,2.69E-87
1.48E-90,82,311,Hyperthyroidism,D006980,114,7.74E-87
7.86E-91,73,206,Dyssomnias,D020920,11,4.12E-87
1.43E-90,77,250,Cavernous Hemangioma of Brain,D020786,57,7.50E-87
1.43E-90,77,250,Amnesia,D000647,56,7.50E-87
7.86E-91,73,206,"Lymphoproliferative Syndrome, X-Linked, 2",C564469,8,4.12E-87
7.86E-91,73,206,Urethral Obstruction,D014524,7,4.12E-87
1.14E-90,74,217,"Aneurysm, Dissecting",D000784,18,5.98E-87
1.71E-90,78,262,Creutzfeldt-Jakob disease,D007562,75,8.94E-87
1.14E-90,74,217,Low Back Pain,D017116,17,5.98E-87
1.52E-90,76,239,Antiphospholipid Syndrome,D016736,44,7.93E-87
1.21E-90,73,207,Esophageal Diseases,D004935,8,6.31E-87
2.41E-90,78,263,Prion Diseases,D017096,73,1.26E-86
1.72E-90,74,218,Hypertrophy,D006984,18,8.98E-87
1.72E-90,74,218,Siderosis,D012806,18,8.98E-87
2.08E-90,75,229,alpha 1-Antitrypsin Deficiency,D019896,34,1.09E-86
3.67E-90,89,415,Trichohepatoenteric Syndrome,C565627,242,1.92E-86
2.93E-90,77,252,Congenital arteriovenous malformation,D001165,57,1.53E-86
2.93E-90,77,252,Necrosis,D009336,55,1.53E-86
2.57E-90,74,219,Dysequilibrium syndrome,C535731,24,1.34E-86
1.84E-90,73,208,Idiopathic Hypoparathyroidism,D007011,9,9.64E-87
4.71E-90,84,342,Hereditary hemochromatosis,D006432,152,2.46E-86
3.85E-90,74,220,Hepatic Form of Wilson Disease,D006527,24,2.01E-86
4.28E-90,73,210,Osteitis Fibrosa Disseminata,D005357,12,2.23E-86
6.62E-90,75,232,"Dysautonomia, Familial",D004402,40,3.45E-86
5.74E-90,74,221,Norrie disease,C537849,22,3.00E-86
6.62E-90,75,232,Sweet Syndrome,D016463,35,3.45E-86
1.07E-89,84,345,"Epilepsy, Temporal Lobe",D004833,160,5.54E-86
1.42E-89,114,941,Coronary heart disease,D003327,797,7.36E-86
6.49E-90,73,211,Multiple congenital anomalies,D000015,15,3.38E-86
6.49E-90,73,211,Pyle metaphyseal dysplasia,C536252,14,3.38E-86
9.61E-90,76,244,Nephrosis,D009401,49,5.00E-86
6.49E-90,73,211,"Cystadenoma, Serous",D018293,11,3.38E-86
8.54E-90,74,222,Intermittent Claudication,D007383,24,4.45E-86
8.54E-90,74,222,Pregnancy in Diabetics,D011254,22,4.45E-86
1.55E-89,82,319,Familial multiple trichoepitheliomata,C536611,136,8.05E-86
1.41E-89,75,234,Hernia,D006547,41,7.34E-86
1.27E-89,74,223,Sarcopenia,D055948,26,6.59E-86
1.27E-89,74,223,Chronic Lung Injury,D055370,23,6.59E-86
1.27E-89,74,223,Asphyxia Neonatorum,D001238,23,6.59E-86
1.27E-89,74,223,Coronary Thrombosis,D003328,23,6.59E-86
1.48E-89,73,213,3-Methylglutaconic aciduria type 2,D056889,16,7.69E-86
9.90E-90,72,202,Glossitis,D005928,3,5.15E-86
9.90E-90,72,202,Sciatica,D012585,3,5.15E-86
3.00E-89,75,236,Moyamoya disease 1,C536991,41,1.55E-85
2.23E-89,73,214,Growth hormone excess,C531600,15,1.16E-85
2.23E-89,73,214,SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME,C535780,15,1.16E-85
2.78E-89,74,225,Asbestosis,D001195,26,1.44E-85
4.83E-89,92,476,Heart Diseases,D006331,292,2.50E-85
9.90E-90,72,202,"Schizophrenia, Disorganized",D012562,2,5.15E-86
9.90E-90,72,202,Osteoma cutis,C562735,2,5.15E-86
9.90E-90,72,202,Pituitary Apoplexy,D010899,2,5.15E-86
6.42E-90,72,201,Clonal Evolution,D060965,1,3.35E-86
6.42E-90,72,201,PARIETAL FORAMINA 1,C566827,1,3.35E-86
6.42E-90,72,201,Tympanosclerosis,D063371,1,3.35E-86
6.42E-90,72,201,Parietal Foramina With Cleidocranial Dysplasia,C566825,1,3.35E-86
6.42E-90,72,201,"Vasculitis, Central Nervous System",D020293,1,3.35E-86
6.42E-90,72,201,"Amelogenesis Imperfecta, Type IV",C566293,1,3.35E-86
6.42E-90,72,201,Familial hypophosphatemia,D007015,1,3.35E-86
6.42E-90,72,201,"Microphthalmia, Posterior, With Retinitis Pigmentosa, Foveoschisis, And Optic Disc Drusen",C567024,1,3.35E-86
6.42E-90,72,201,NANOPHTHALMOS 2 (disorder),C563700,1,3.35E-86
1.52E-89,72,203,Starvation,D013217,3,7.90E-86
1.52E-89,72,203,Acampomelic Campomelic Dysplasia,D055036,3,7.90E-86
4.36E-89,75,237,Epiretinal Membrane,D019773,40,2.25E-85
3.35E-89,73,215,Smoldering myeloma,D000075122,16,1.74E-85
4.10E-89,74,226,"MICROPHTHALMIA, SYNDROMIC 7",C537466,29,2.12E-85
2.33E-89,72,204,"Peroxisome Biogenesis Disorder, Complementation Group H",C566626,5,1.21E-85
2.33E-89,72,204,Pneumoperitoneum,D011027,4,1.21E-85
6.04E-89,74,227,"Hyalinosis, Segmental Glomerular",D005923,28,3.13E-85
3.57E-89,72,205,Chromosome 17 trisomy,C538044,6,1.85E-85
9.13E-89,75,239,Moyamoya Disease,D009072,46,4.71E-85
1.39E-88,86,384,Gastroesophageal reflux disease,D005764,219,7.16E-85
8.88E-89,74,228,Bowen's Disease,D001913,30,4.59E-85
8.88E-89,74,228,Bone necrosis,D010020,29,4.59E-85
5.45E-89,72,206,"Macular Degeneration, Age-Related, 1",C566411,7,2.82E-85
8.88E-89,74,228,Hallopeau-Siemens Disease,D016108,28,4.59E-85
5.45E-89,72,206,Infantile myofibromatosis,C562978,6,2.82E-85
1.32E-88,75,240,Laryngeal Diseases,D007818,47,6.79E-85
8.29E-89,72,207,Barakat syndrome,C537907,10,4.29E-85
1.32E-88,75,240,Multiple Endocrine Neoplasia,D009377,44,6.79E-85
8.29E-89,72,207,Hallermann's Syndrome,D006210,9,4.29E-85
1.12E-88,73,218,"Bone Cysts, Aneurysmal",D017824,20,5.79E-85
1.12E-88,73,218,Pathological accumulation of air in tissues,D004646,19,5.79E-85
8.29E-89,72,207,Wasting Syndrome,D019282,8,4.29E-85
8.29E-89,72,207,Digestive System Disorders,D004066,8,4.29E-85
8.29E-89,72,207,Chondromalacia,D002357,8,4.29E-85
1.77E-88,80,301,Myocardial Failure,D006333,103,9.12E-85
1.84E-88,78,276,Intraepithelial Neoplasia,D002278,82,9.50E-85
1.26E-88,72,208,Testicular Hydrocele,D006848,12,6.49E-85
1.26E-88,72,208,Transfusion-Related Acute Lung Injury,D000073617,11,6.49E-85
1.67E-88,73,219,Polyarteritis Nodosa,D010488,25,8.60E-85
1.90E-88,74,230,Isochromosomes,D018404,37,9.80E-85
1.26E-88,72,208,Osteochondritis Dissecans,D010008,10,6.49E-85
1.67E-88,73,219,Protein Misfolding Disorders,D057165,21,8.60E-85
1.26E-88,72,208,Sialuria,D029461,9,6.49E-85
1.26E-88,72,208,Anuria,D001002,8,6.49E-85
1.26E-88,72,208,Chorea Acanthocytosis Syndrome,D054546,8,6.49E-85
2.48E-88,73,220,"Hemangioma, Cavernous",D006392,22,1.28E-84
1.90E-88,72,209,Germinoma,D018237,10,9.80E-85
4.15E-88,79,291,Rett Syndrome,D015518,107,2.13E-84
2.88E-88,72,210,"Skin Diseases, Bacterial",D017192,13,1.48E-84
2.88E-88,72,210,Epithelioid hemangioendothelioma,D018323,12,1.48E-84
4.05E-88,74,232,Bladder neck obstruction,D001748,34,2.08E-84
2.88E-88,72,210,Secondary Parkinson Disease,D010302,10,1.48E-84
5.85E-88,80,305,Ependymoma,D004806,110,3.00E-84
5.62E-88,75,244,"Osteoporosis, Postmenopausal",D015663,46,2.88E-84
4.33E-88,72,211,Cellulitis,D002481,14,2.23E-84
6.74E-88,76,256,Hamartoma,D006222,65,3.45E-84
4.33E-88,72,211,Tonsillitis,D014069,13,2.23E-84
5.43E-88,73,222,Placental Insufficiency,D010927,25,2.78E-84
4.33E-88,72,211,Juvenile hemochromatosis,C537247,12,2.23E-84
1.12E-87,96,565,Metabolic Diseases,D008659,383,5.73E-84
9.87E-88,77,269,Iron Overload,D019190,78,5.05E-84
8.02E-88,73,223,Gestational trophoblastic disease,D031901,29,4.10E-84
6.51E-88,72,212,Ileus,D045823,13,3.33E-84
9.76E-88,72,213,"Heart Failure, Systolic",D054143,15,4.99E-84
1.18E-87,73,224,Autoimmune Lymphoproliferative Syndrome,D056735,26,6.02E-84
1.18E-87,73,224,Scrub Typhus,D012612,26,6.02E-84
2.86E-87,109,856,Neurodegenerative Disorders,D019636,689,1.46E-83
3.01E-87,83,352,Aplasia Cutis Congenita,D004476,161,1.53E-83
6.87E-88,71,202,Mandibular Diseases,D008336,2,3.52E-84
6.87E-88,71,202,"Chorea, Senile",D002819,2,3.52E-84
6.87E-88,71,202,Vascular Hemostatic Disorders,D020141,2,3.52E-84
6.87E-88,71,202,"Cirrhosis, Familial",C566123,2,3.52E-84
6.87E-88,71,202,Inappropriate ADH Syndrome,D007177,2,3.52E-84
6.87E-88,71,202,Tinea Versicolor,D014010,2,3.52E-84
4.49E-88,71,201,"Aphasia, Mixed",D001037,1,2.31E-84
4.49E-88,71,201,"Hematoma, Epidural, Spinal",D046748,1,2.31E-84
4.49E-88,71,201,Necrotizing Ulcerative Gingivitis,D005892,1,2.31E-84
4.49E-88,71,201,"Thrombophilia, Familial, Due To Decreased Release Of Tissue Plasminogen Activator",C567341,1,2.31E-84
4.49E-88,71,201,Back Pain without Radiation,D001416,1,2.31E-84
4.49E-88,71,201,Choreoathetosis And Congenital Hypothyroidism,C567034,1,2.31E-84
4.49E-88,71,201,"Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative",C565533,1,2.31E-84
4.49E-88,71,201,Thrombophilia due to Thrombomodulin Defect,C566057,1,2.31E-84
4.49E-88,71,201,"Subdural Hematoma, Traumatic",D006408,1,2.31E-84
4.49E-88,71,201,Embolus,D004617,1,2.31E-84
4.49E-88,71,201,Hydroxyprolinemia,C562669,1,2.31E-84
1.05E-87,71,203,Hereditary Diffuse Leukoencephalopathy with Spheroids,C580150,4,5.36E-84
1.05E-87,71,203,Calcium Pyrophosphate Dihydrate Deposition,D002805,4,5.36E-84
1.05E-87,71,203,Sclerosing lymphocytic lobulitis,C537524,3,5.36E-84
1.05E-87,71,203,Endemic Tyrolean Infantile Cirrhosis,C566132,3,5.36E-84
1.05E-87,71,203,Chromosome 18q syndrome,C536580,3,5.36E-84
1.05E-87,71,203,ZAP70 deficiency,C536722,3,5.36E-84
1.05E-87,71,203,"Chromosome 18, trisomy 18q",C538308,3,5.36E-84
1.05E-87,71,203,INFLAMMATORY BOWEL DISEASE 5,C565234,3,5.36E-84
1.60E-87,71,204,"Empyema, Pleural",D016724,6,8.13E-84
3.30E-87,75,249,Osteoarthritis of hip,D015207,54,1.68E-83
3.24E-87,72,216,Meningomyelocele,D008591,20,1.65E-83
3.24E-87,72,216,Piebaldism,D016116,17,1.65E-83
3.24E-87,72,216,Primary Progressive Aphasia (disorder),D018888,16,1.65E-83
2.42E-87,71,205,Serum Sickness,D012713,6,1.23E-83
2.42E-87,71,205,Ectopic Pregnancy,D011271,6,1.23E-83
2.42E-87,71,205,Urinary Retention,D016055,5,1.23E-83
3.67E-87,71,206,Prodromal Symptoms,D062706,9,1.87E-83
3.67E-87,71,206,Liver Abscess,D008100,7,1.87E-83
1.00E-86,76,264,Malignant Fibrous Histiocytoma,D051677,67,5.09E-83
7.13E-87,72,218,Idiopathic Nephrotic Syndrome,C535761,18,3.63E-83
5.54E-87,71,207,Histiocytoma,D051642,7,2.82E-83
5.54E-87,71,207,Asthenia,D001247,7,2.82E-83
1.10E-86,74,241,Hyperparathyroidism,D006961,42,5.58E-83
1.31E-86,77,277,Drug toxicity,D064420,82,6.65E-83
8.34E-87,71,208,Meleda Disease,D007645,12,4.24E-83
1.15E-86,73,230,Tubular Aggregate Myopathy,D020914,32,5.83E-83
1.05E-86,72,219,Nephrosclerosis,D009400,20,5.35E-83
8.34E-87,71,208,Lentivirus Infections,D016180,9,4.24E-83
8.34E-87,71,208,Wernicke Encephalopathy,D014899,8,4.24E-83
8.34E-87,71,208,Histiocytoid hemangioma,D006391,8,4.24E-83
1.57E-86,74,242,Pancreatic Diseases,D010182,51,7.98E-83
1.57E-86,74,242,Cystadenoma,D003537,45,7.98E-83
1.25E-86,71,209,"FUNDUS DYSTROPHY, PSEUDOINFLAMMATORY, OF SORSBY",C564992,10,6.36E-83
1.25E-86,71,209,Bisphosphonate-associated osteonecrosis,D059266,9,6.36E-83
2.24E-86,74,243,Fabry Disease,D000795,46,1.14E-82
2.77E-86,78,292,Multiple Endocrine Neoplasia Type 1,D018761,97,1.40E-82
2.29E-86,72,221,Cholesteatoma,D002781,22,1.16E-82
2.29E-86,72,221,Aortic Diseases,D001018,22,1.16E-82
1.88E-86,71,210,Jaw Keratocyst,D009807,10,9.53E-83
3.74E-86,78,293,Ischemia,D007511,99,1.89E-82
4.62E-86,77,281,"Myocardial Diseases, Secondary",D009202,85,2.34E-82
2.81E-86,71,211,Pineal Gland Neoplasm,D010871,14,1.42E-82
5.15E-86,75,257,Marinesco-Sjogren syndrome,D013132,67,2.60E-82
4.92E-86,72,223,"Hypophosphatemic Rickets, X-Linked Dominant",D053098,28,2.49E-82
8.42E-86,84,380,Visual seizure,D012640,195,4.25E-82
7.20E-86,75,258,FRIEDREICH ATAXIA 1,C565561,62,3.63E-82
7.20E-86,75,258,Gestational Diabetes,D016640,61,3.63E-82
9.77E-86,82,351,Nephrotic Syndrome,D009404,169,4.93E-82
7.24E-86,73,235,Anthrax disease,D000881,38,3.65E-82
7.20E-86,72,224,Dysautonomia,D054969,32,3.63E-82
6.24E-86,71,213,Cannabis Abuse,D002189,15,3.15E-82
6.24E-86,71,213,Body Temperature Changes,D001832,14,3.15E-82
6.24E-86,71,213,Intravascular hemolysis,D006461,13,3.15E-82
1.01E-85,75,259,Migraine with Aura,D020325,65,5.07E-82
3.05E-86,70,201,"Plasma Cell Granuloma, Pulmonary",D016726,2,1.54E-82
1.40E-85,75,260,Uremia,D014511,63,7.07E-82
4.63E-86,70,202,Pemphigoid Gestationis,D006559,2,2.34E-82
4.63E-86,70,202,Conversion disorder,D003291,2,2.34E-82
4.63E-86,70,202,Proteus-Like Syndrome (disorder),D016715,2,2.34E-82
4.63E-86,70,202,Swine Vesicular Disease,D013555,2,2.34E-82
3.05E-86,70,201,"Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant",C567411,1,1.54E-82
3.05E-86,70,201,Erythrokeratodermia with ataxia,C535738,1,1.54E-82
3.05E-86,70,201,"Keratoderma, Palmoplantar, Norrbotten Recessive Type",C565454,1,1.54E-82
3.05E-86,70,201,Band Heterotopia of Brain,C563950,1,1.54E-82
2.16E-85,77,286,"PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE",D020734,90,1.09E-81
7.01E-86,70,203,Halo nevus,D055882,3,3.54E-82
7.01E-86,70,203,"Nevus, Intradermal",D018330,3,3.54E-82
2.14E-85,73,238,Hemangioblastoma,D018325,38,1.08E-81
2.72E-85,75,262,Cerebral Hemorrhage,D002543,64,1.37E-81
2.22E-85,72,227,High altitude pulmonary edema,C535833,29,1.12E-81
1.06E-85,70,204,Pallidopontonigral degeneration,C563003,4,5.33E-82
2.03E-85,71,216,ABLEPHARON-MACROSTOMIA SYNDROME,C535557,17,1.02E-81
2.03E-85,71,216,Papillon-Lefevre Disease,D010214,16,1.02E-81
3.50E-85,76,275,Venous Thrombosis,D020246,85,1.76E-81
1.59E-85,70,205,Postural Orthostatic Tachycardia Syndrome,D054972,6,8.03E-82
1.59E-85,70,205,Embryo Disintegration,D020964,6,8.03E-82
1.59E-85,70,205,Neointima Formation,D058426,5,8.03E-82
1.59E-85,70,205,"Gastritis, Hypertrophic",D005758,5,8.03E-82
3.62E-85,74,251,Kidney Calculi,D007669,57,1.82E-81
2.99E-85,71,217,Amyloid angiopathy,C538248,18,1.50E-81
5.09E-85,74,252,Conn Syndrome,D006929,57,2.56E-81
5.09E-85,74,252,Ameloblastoma,D000564,56,2.56E-81
5.37E-85,70,208,Todd Paralysis,D010243,9,2.70E-81
5.37E-85,70,208,CCHS WITH HIRSCHSPRUNG DISEASE,C536209,9,2.70E-81
5.37E-85,70,208,Prehypertension,D058246,8,2.70E-81
9.47E-85,71,220,"Charcot-Marie-Tooth Disease, Type Ia (disorder)",D002607,26,4.75E-81
9.47E-85,71,220,Hereditary hemorrhagic telangiectasia,D013683,22,4.75E-81
8.01E-85,70,209,Hypoproteinemia,D007019,12,4.02E-81
8.01E-85,70,209,Pyogenic granuloma,D017789,10,4.02E-81
8.01E-85,70,209,Behavioral tic,D020323,10,4.02E-81
1.40E-84,74,255,Progressive supranuclear palsy,D013494,62,7.00E-81
1.40E-84,74,255,Mitral Valve Prolapse Syndrome,D008945,62,7.00E-81
1.19E-84,70,210,Hypophosphatasia,D007014,16,5.98E-81
1.90E-84,75,268,Prediabetes syndrome,D011236,73,9.53E-81
1.19E-84,70,210,Lysinuric Protein Intolerance,C562687,12,5.98E-81
1.19E-84,70,210,Hereditary Autoinflammatory Diseases,D056660,10,5.98E-81
1.77E-84,70,211,"SPHEROCYTOSIS, TYPE 1 (disorder)",C567159,13,8.87E-81
1.77E-84,70,211,Tic disorder,D013981,12,8.87E-81
1.77E-84,70,211,Relapsing Fever,D012061,11,8.87E-81
3.53E-84,73,246,Drug Resistant Epilepsy,D000069279,55,1.76E-80
3.78E-84,74,258,Shy-Drager Syndrome,D012791,71,1.89E-80
2.94E-84,71,223,Intervertebral disc disorder,C535531,23,1.47E-80
2.62E-84,70,212,Myoepithelioma,D009208,15,1.31E-80
2.62E-84,70,212,Empyema,D004653,14,1.31E-80
2.62E-84,70,212,"HYPERTRICHOSIS, CONGENITAL GENERALIZED",C538388,13,1.31E-80
2.62E-84,70,212,"Reticuloendotheliosis, X-linked",C538362,12,1.31E-80
7.49E-84,80,339,Pulmonary Hypertension,D006976,142,3.73E-80
6.99E-84,73,248,Stereotyped Behavior,D013239,71,3.48E-80
7.29E-84,74,260,Varicosity,D014648,71,3.63E-80
8.38E-84,72,237,Cerebral Amyloid Angiopathy,D016657,42,4.18E-80
3.03E-84,69,202,Ligneous conjunctivitis,C566897,2,1.51E-80
3.03E-84,69,202,"Peeling skin syndrome, acral type",C536316,2,1.51E-80
1.42E-83,81,356,Proteinuria,D011507,169,7.08E-80
4.55E-84,69,203,Troyer syndrome,C536858,4,2.27E-80
2.01E-84,69,201,"HYPERPIGMENTATION, FAMILIAL PROGRESSIVE",C564163,1,1.01E-80
2.01E-84,69,201,Idiopathic Hypercatabolic Hypoproteinemia,D011504,1,1.01E-80
2.01E-84,69,201,Weaver-Like Syndrome,C562443,1,1.01E-80
2.01E-84,69,201,Skin Mastocytoma,D054705,1,1.01E-80
2.01E-84,69,201,"Upper Extremity Deformities, Congenital",D038062,1,1.01E-80
2.01E-84,69,201,"Melanosis, Universal",C563594,1,1.01E-80
2.01E-84,69,201,Nasopharyngitis,D009304,1,1.01E-80
1.37E-83,73,250,Beckwith-Wiedemann Syndrome,D001506,57,6.84E-80
1.29E-83,71,227,"Parkinson Disease, Familial, Type 1",C566823,31,6.44E-80
1.23E-83,70,216,Familial benign pemphigus,D016506,20,6.15E-80
6.82E-84,69,204,Esophageal and Gastric Varices,D004932,4,3.40E-80
6.82E-84,69,204,Allanson Pantzar McLeod syndrome,C537048,4,3.40E-80
6.82E-84,69,204,Renal Tubular Dysgenesis With Choanal Atresia And Athelia,C567491,4,3.40E-80
6.82E-84,69,204,"Chromosome 1, monosomy 1p",C535591,4,3.40E-80
1.02E-83,69,205,Flavivirus Infections,D018177,6,5.08E-80
1.02E-83,69,205,Lead Poisoning,D007855,6,5.08E-80
1.86E-83,71,228,Meniere Disease,D008575,31,9.27E-80
3.26E-83,77,303,Aortic Valve Stenosis,D001024,118,1.62E-79
2.68E-83,71,229,Folic Acid Deficiency,D005494,30,1.33E-79
1.52E-83,69,206,Sprains and Strains,D013180,6,7.57E-80
1.52E-83,69,206,Birdshot chorioretinopathy,C537630,6,7.57E-80
3.40E-83,72,241,Peutz-Jeghers Syndrome,D010580,51,1.69E-79
2.64E-83,70,218,Paroxysmal nonkinesigenic dyskinesia,C537181,19,1.31E-79
2.64E-83,70,218,Myomatous neoplasm,D019042,19,1.31E-79
2.26E-83,69,207,Neuropil Threads,D019600,11,1.13E-79
4.35E-83,75,278,Werner Syndrome,D014898,88,2.16E-79
4.35E-83,75,278,Aortic Aneurysm,D001014,86,2.16E-79
2.26E-83,69,207,Epithelioid and spindle cell nevus,D018332,9,1.13E-79
2.26E-83,69,207,Adenomyoma,D018194,7,1.13E-79
5.91E-83,75,279,Fragile X Syndrome,D005600,86,2.93E-79
3.36E-83,69,208,Necrotizing fasciitis,D019115,10,1.67E-79
9.59E-83,92,552,Dementia,D003704,385,4.75E-79
8.14E-83,70,221,Peritoneal Fibrosis,D056627,24,4.04E-79
7.35E-83,69,210,"SYNOVITIS, GRANULOMATOUS, WITH UVEITIS AND CRANIAL NEUROPATHIES (disorder)",C538157,14,3.65E-79
1.47E-82,75,282,Tactile Allodynia,D006930,85,7.25E-79
1.18E-82,70,222,Acquired CJD,C538481,27,5.85E-79
1.77E-82,74,270,Protein Deficiency,D011488,75,8.77E-79
1.08E-82,69,211,Syringomyelia,D013595,13,5.38E-79
1.98E-82,75,283,Weight Gain,D015430,100,9.79E-79
1.98E-82,75,283,Post-Traumatic Stress Disorder,D013313,96,9.79E-79
1.08E-82,69,211,Retinitis,D012173,11,5.38E-79
1.98E-82,75,283,Frontotemporal Lobar Degeneration,D057174,90,9.79E-79
2.42E-82,74,271,Central Serous Chorioretinopathy,D056833,77,1.20E-78
3.08E-82,79,339,Cyst,D003560,155,1.52E-78
2.28E-82,71,235,Dupuytren Contracture,D004387,40,1.13E-78
1.59E-82,69,212,"Depressive Disorder, Treatment-Resistant",D061218,12,7.89E-79
2.34E-82,69,213,Epithelial cyst,D004814,13,1.16E-78
1.28E-82,68,201,Arterivirus Infections,D018174,3,6.37E-79
1.28E-82,68,201,Trimethylaminuria,C536561,2,6.37E-79
3.43E-82,69,214,Choroidal Neovascularization,D020256,15,1.69E-78
6.50E-82,75,287,Cholera,D002771,103,3.20E-78
2.87E-82,68,203,Fahr's syndrome (disorder),C536275,5,1.42E-78
1.92E-82,68,202,Renal Artery Obstruction,D012078,2,9.50E-79
8.23E-82,76,301,Hyperhomocysteinemia,D020138,105,4.05E-78
1.28E-82,68,201,Intrathoracic Goiters,D006045,1,6.37E-79
1.28E-82,68,201,Myelocerebellar Disorder,C563233,1,6.37E-79
1.28E-82,68,201,"Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II",C565531,1,6.37E-79
1.28E-82,68,201,"Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I",C565532,1,6.37E-79
1.28E-82,68,201,Reflex Sympathetic Dystrophy,D012019,1,6.37E-79
9.25E-82,77,315,Disease Exacerbation,D018450,128,4.56E-78
2.87E-82,68,203,Autoimmune Diseases of the Nervous System,D020274,3,1.42E-78
2.87E-82,68,203,"Osteopetrosis, mild autosomal recessive form",C536059,3,1.42E-78
4.27E-82,68,204,"Skin Diseases, Vascular",D017445,5,2.10E-78
4.27E-82,68,204,Pseudopapilledema,C562401,4,2.10E-78
6.33E-82,68,205,COWDEN-LIKE SYNDROME (disorder),C567337,6,3.12E-78
1.52E-81,74,277,Adrenal Cortical Adenoma,D018246,81,7.50E-78
6.33E-82,68,205,Multiple Chemical Sensitivity,D018777,5,3.12E-78
1.06E-81,69,217,Neonatal Systemic lupus erythematosus,C536397,19,5.23E-78
1.81E-81,71,241,Congenital defects,Q000002,51,8.92E-78
1.39E-81,68,207,Altitude Sickness,D000532,7,6.82E-78
2.04E-81,68,208,Chromosome Breaks,D019457,8,1.01E-77
4.96E-81,79,350,insulinoma,D007340,162,2.44E-77
4.32E-81,70,232,ACTH-Secreting Pituitary Adenoma,D049913,33,2.12E-77
6.99E-81,72,257,Diaphragmatic Hernia,D006548,61,3.43E-77
6.97E-81,71,245,Diabetic Cardiomyopathies,D058065,48,3.43E-77
1.03E-80,80,368,Aortic Valve Insufficiency,D001022,187,5.04E-77
6.45E-81,68,211,Fissured tongue,D014063,18,3.17E-77
6.45E-81,68,211,"Dermatitis, Phototoxic",D017484,13,3.17E-77
6.45E-81,68,211,"LEUKOENCEPHALOPATHY, BRAIN CALCIFICATIONS, AND CYSTS",C000598644,11,3.17E-77
2.30E-80,84,436,"Pancreatitis, Chronic",D050500,256,1.13E-76
1.38E-80,69,224,Apathy,D057565,25,6.77E-77
1.37E-80,68,213,Tricuspid Valve Insufficiency,D014262,14,6.73E-77
1.37E-80,68,213,ALZHEIMER DISEASE 2,C536595,13,6.73E-77
2.43E-80,70,237,Language Disorders,D007806,48,1.19E-76
1.18E-80,67,202,Histiocytosis with joint contractures and sensorineural deafness,C538322,3,5.81E-77
4.92E-80,77,330,Dental caries,D003731,161,2.40E-76
1.75E-80,67,203,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B (disorder)",C537989,5,8.60E-77
2.90E-80,68,215,Reactive hypoglycemia,D007003,15,1.42E-76
1.18E-80,67,202,"Granuloma, Respiratory Tract",D015769,2,5.81E-77
1.18E-80,67,202,MACROCEPHALY/AUTISM SYNDROME,C565342,2,5.81E-77
7.98E-81,67,201,"Atypical Mycobacteriosis, Familial, X-Linked 2",C567068,1,3.92E-77
7.98E-81,67,201,"INFLAMMATORY BOWEL DISEASE 28, AUTOSOMAL RECESSIVE",C567728,1,3.92E-77
7.98E-81,67,201,"Infections, Bunyavirus",D002044,1,3.92E-77
7.98E-81,67,201,"Varicella, Severe Recurrent",C563458,1,3.92E-77
1.75E-80,67,203,Jansen type metaphyseal chondrodysplasia,C537564,3,8.60E-77
1.75E-80,67,203,Erythroplasia,D004919,3,8.60E-77
1.75E-80,67,203,"Chondrodysplasia, blomstrand type",C537914,3,8.60E-77
7.23E-80,79,361,Bronchopulmonary Dysplasia,D001997,173,3.53E-76
3.82E-80,67,205,Leg Length Inequality,D007870,7,1.87E-76
3.82E-80,67,205,"Cutis laxa, x-linked",C537860,6,1.87E-76
3.82E-80,67,205,Postoperative Complications,D011183,5,1.87E-76
3.82E-80,67,205,Ataxic cerebral palsy,C562856,5,1.87E-76
8.12E-80,69,229,Harlequin Fetus,D017490,31,3.97E-76
5.61E-80,67,206,Cardiovirus Infections,D018188,8,2.75E-76
1.37E-79,77,334,"Ovarian Failure, Premature",D016649,152,6.69E-76
1.60E-79,72,267,Machado-Joseph Disease,D017827,71,7.80E-76
8.23E-80,67,207,Hookworm Infections,D006725,8,4.02E-76
1.83E-79,70,243,"Scoliosis, unspecified",D012600,49,8.92E-76
1.76E-79,67,209,Poikiloderma with Neutropenia,C565820,11,8.59E-76
1.76E-79,67,209,POEMS Syndrome,D016878,9,8.59E-76
1.76E-79,67,209,Quebec platelet disorder,C536260,9,8.59E-76
2.56E-79,67,210,Histiocytosis,D015614,12,1.25E-75
2.56E-79,67,210,Urolithiasis,D052878,12,1.25E-75
5.37E-79,72,271,Chest Pain,D002637,73,2.61E-75
6.37E-79,71,259,Spinocerebellar Ataxia Type 1,D020754,67,3.10E-75
6.78E-79,70,247,Leukoplakia,D007971,52,3.30E-75
1.66E-78,78,359,"Muscular Dystrophy, Duchenne",D020388,175,8.08E-75
4.81E-79,66,201,CORNEAL DYSTROPHY AND PERCEPTIVE DEAFNESS,C535473,3,2.35E-75
1.73E-78,73,288,Atrial Premature Complexes,D018880,94,8.38E-75
2.00E-78,74,302,Tauopathies,D024801,113,9.71E-75
7.09E-79,66,202,Acute Generalized Exanthematous Pustulosis,D056150,3,3.45E-75
7.09E-79,66,202,Psychomotor Agitation,D011595,3,3.45E-75
7.09E-79,66,202,"Arthrogryposis multiplex congenita, distal, X-linked",C535380,2,3.45E-75
7.09E-79,66,202,"CHARCOT-MARIE-TOOTH DISEASE, TYPE 4D",C535716,2,3.45E-75
7.09E-79,66,202,"CD8 Deficiency, Familial",C563824,2,3.45E-75
2.97E-78,71,264,Stereotypic Movement Disorder,D019956,82,1.44E-74
4.81E-79,66,201,"Familial Mediterranean Fever, Autosomal Dominant",C565021,1,2.35E-75
4.81E-79,66,201,Hirschsprung disease type 3,C538121,1,2.35E-75
4.81E-79,66,201,Forney Robinson Pascoe syndrome,C537269,1,2.35E-75
4.81E-79,66,201,Keratitis Fugax Hereditaria,C563650,1,2.35E-75
4.81E-79,66,201,Palindromic rheumatism,C538103,1,2.35E-75
4.81E-79,66,201,T cell immunodeficiency primary,C536780,1,2.35E-75
4.81E-79,66,201,Familial Cold Autoinflammatory Syndrome 2,C567090,1,2.35E-75
4.81E-79,66,201,Cerebrofaciothoracic Dysplasia,C565862,1,2.35E-75
1.04E-78,66,203,Lewy Body Variant of Alzheimer Disease,C565078,3,5.07E-75
3.41E-78,69,240,Skin Abnormalities,D012868,55,1.66E-74
1.53E-78,66,204,Ergotism,D004881,5,7.43E-75
1.53E-78,66,204,Hyperphosphatasemia with bone disease,C537701,4,7.43E-75
4.75E-78,66,207,Chromosome 21 monosomy,C537108,7,2.31E-74
6.90E-78,66,208,"Hyperbilirubinemia, Neonatal",D051556,9,3.35E-74
2.79E-77,73,298,Muscle Rigidity,D009127,111,1.35E-73
5.36E-77,78,374,Congenital contractural arachnodactyly,C536211,188,2.60E-73
5.86E-77,71,274,Manic,D001714,87,2.84E-73
4.33E-77,66,213,Semantic Dementia,D057180,13,2.10E-73
6.32E-77,68,237,Lytic lesion,D010014,39,3.06E-73
6.21E-77,66,214,Alexander Disease,D038261,16,3.01E-73
1.41E-76,73,304,Lewy Body Disease,D020961,120,6.79E-73
1.41E-76,73,304,Memory Loss,D008569,114,6.79E-73
8.88E-77,66,215,Shwachman syndrome,C537330,17,4.30E-73
4.12E-77,65,202,Familial Paget's disease of bone,C538098,2,2.00E-73
4.12E-77,65,202,Compartment syndromes,D003161,2,2.00E-73
1.60E-76,69,252,"Stress, Psychological",D013315,59,7.72E-73
2.82E-77,65,201,"Deafness, Autosomal Recessive 28",C565218,1,1.37E-73
2.82E-77,65,201,Immunodeficiency due to Defect in CD3-Zeta,C565712,1,1.37E-73
6.01E-77,65,203,Epidermolysis Bullosa Pruriginosa,C563192,3,2.91E-73
8.74E-77,65,204,GIANT AXONAL NEUROPATHY 1,D056768,5,4.23E-73
8.74E-77,65,204,Sex Chromosome Aberrations,D012729,5,4.23E-73
8.74E-77,65,204,Struma Ovarii,D013330,4,4.23E-73
1.27E-76,65,205,"Bare Lymphocyte Syndrome, Type I",C565759,6,6.14E-73
1.27E-76,65,205,Cyclical vomiting syndrome (disorder),C536228,5,6.14E-73
1.27E-76,65,205,"Osteoarthritis, Spine",D055013,5,6.14E-73
3.84E-76,65,208,Iron Metabolism Disorders,D019189,9,1.85E-72
1.07E-75,70,271,Spina Bifida,D016135,83,5.17E-72
7.94E-76,65,210,"Color Blindness, Blue",D003117,14,3.84E-72
1.46E-75,66,223,Hereditary pyropoikilocytosis,C563004,32,7.03E-72
3.30E-75,72,302,Neurologic Symptoms,D009461,115,1.59E-71
2.87E-75,66,225,Achondroplasia,D000130,26,1.39E-71
2.32E-75,64,202,"DIABETES MELLITUS, INSULIN-DEPENDENT, 4",C563959,4,1.12E-71
4.71E-75,65,215,"Opitz GBBB Syndrome, X-Linked",C567932,20,2.27E-71
9.42E-75,72,306,"Cleft palate, isolated",D002972,123,4.54E-71
2.32E-75,64,202,Mucocele,D009078,2,1.12E-71
1.05E-74,70,279,Vesico-Ureteral Reflux,D014718,94,5.05E-71
6.68E-75,65,216,Sandhoff Disease,D012497,17,3.22E-71
4.86E-75,64,204,Scarlet Fever,D012541,6,2.34E-71
1.08E-74,69,266,"Hyperlipidemia, Familial Combined",D006950,73,5.22E-71
1.49E-74,75,352,Spinal Muscular Atrophy,D009134,174,7.15E-71
4.86E-75,64,204,Laryngeal papillomatosis,C537876,4,2.34E-71
9.46E-75,65,217,Tooth Loss,D016388,17,4.56E-71
9.46E-75,65,217,Overnutrition,D044343,17,4.56E-71
1.01E-74,64,206,Ceruloplasmin deficiency,C536004,6,4.85E-71
2.85E-74,78,403,Cognition Disorders,D003072,219,1.37E-70
1.45E-74,64,207,Adenofibroma,D000232,7,6.97E-71
2.65E-74,65,220,Epidermolysis Bullosa Simplex,D016110,23,1.28E-70
2.96E-74,64,209,Paramyotonia Congenita (disorder),D020967,13,1.43E-70
3.73E-74,65,221,Hemimegalencephaly,D065705,22,1.79E-70
4.23E-74,64,210,Chondroblastoma,D002804,10,2.03E-70
6.02E-74,64,211,Progressive pseudorheumatoid dysplasia,C535387,14,2.89E-70
1.60E-73,89,623,Polycystic Ovary Syndrome,D011085,465,7.70E-70
1.33E-73,67,249,Cortical Dysplasia,D054220,58,6.40E-70
1.67E-73,73,332,Keratoconus,D007640,157,8.00E-70
1.21E-73,64,213,"CATARACT, MARNER TYPE",C535342,18,5.82E-70
1.83E-73,63,203,"BRACHYDACTYLY, TYPE E1",C566194,4,8.75E-70
1.27E-73,63,202,Acute Cholecystitis,D041881,2,6.09E-70
1.27E-73,63,202,Congenital atransferrinemia,C538259,2,6.09E-70
8.81E-74,63,201,Delayed Hypersensitivity,D006968,1,4.23E-70
8.81E-74,63,201,Polyradiculitis,D011128,1,4.23E-70
8.81E-74,63,201,Dysalbuminemic Hyperthyroxinemia,C566305,1,4.23E-70
8.81E-74,63,201,Immune Hydrops Fetalis,D015160,1,4.23E-70
8.81E-74,63,201,HIV Seropositivity,D006679,1,4.23E-70
1.83E-73,63,203,Dyssegmental dysplasia,C537998,3,8.75E-70
2.62E-73,63,204,"HEMOCHROMATOSIS, TYPE 4",C537249,4,1.26E-69
3.75E-73,63,205,Rudiger syndrome 1,C536189,8,1.80E-69
3.75E-73,63,205,Pure Autonomic Failure,D054970,6,1.80E-69
7.34E-73,65,230,Split hand foot deformity 1,C574275,36,3.51E-69
5.36E-73,63,206,Cervical Migraine Syndrome,D008881,8,2.57E-69
5.36E-73,63,206,Preterm Premature Rupture of Fetal Membranes,D005322,7,2.57E-69
7.64E-73,63,207,Paronychia Inflammation,D010304,10,3.66E-69
2.13E-72,79,442,Agenesis of corpus callosum,D061085,272,1.02E-68
1.85E-72,64,221,Hyperostosis,D015576,23,8.83E-69
3.68E-72,72,330,Developmental Disabilities,D002658,157,1.76E-68
4.36E-72,76,394,"Plaque, Amyloid",D058225,221,2.09E-68
2.19E-72,63,210,Fracture,D050723,12,1.05E-68
1.38E-71,79,452,Cholestasis,D002779,277,6.57E-68
9.53E-72,64,226,Christ-Siemens-Touraine syndrome,D053358,26,4.54E-68
6.74E-72,62,202,"Anemia, Hypochromic Microcytic, With Iron Overload",C567144,4,3.21E-68
2.38E-71,78,437,Atrial Fibrillation,D001281,261,1.13E-67
6.74E-72,62,202,"Taste Disorder, Secondary, Salt",D013651,2,3.21E-68
6.74E-72,62,202,Multiple gastrointestinal atresias (disorder),C562441,2,3.21E-68
6.74E-72,62,202,"Iron Overload, Autosomal Dominant",C565020,2,3.21E-68
6.74E-72,62,202,RAINE SYNDROME,C535282,2,3.21E-68
6.74E-72,62,202,Osteitis Fibrosa Cystica,D010002,2,3.21E-68
4.71E-72,62,201,"Peroxisome Biogenesis Disorder, Complementation Group 13",C566625,1,2.25E-68
4.71E-72,62,201,Serositis,D012700,1,2.25E-68
4.71E-72,62,201,"Spondylocheirodysplasia, Ehlers-Danlos Syndrome-Like",C567340,1,2.25E-68
4.71E-72,62,201,"ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3",C565799,1,2.25E-68
4.71E-72,62,201,"Zinc Deficiency, Neonatal, due to Low Breast Milk Zinc",C564286,1,2.25E-68
4.71E-72,62,201,OROFACIAL CLEFT 8,C565069,1,2.25E-68
4.71E-72,62,201,"Cleft Lip with or without Cleft Palate, Nonsyndromic, 8",C565070,1,2.25E-68
4.71E-72,62,201,Pica Disease,D010842,1,2.25E-68
4.71E-72,62,201,"HEMOSIDEROSIS, SYSTEMIC, DUE TO ACERULOPLASMINEMIA",C565801,1,2.25E-68
9.62E-72,62,203,"HEMOCHROMATOSIS, TYPE 3",C537248,3,4.58E-68
9.62E-72,62,203,Neonatal hemochromatosis,C536394,3,4.58E-68
6.02E-71,70,312,Heartburn,D006356,144,2.87E-67
1.02E-70,77,427,Dwarfism,D004392,262,4.87E-67
1.46E-70,66,260,Wiskott-Aldrich Syndrome,D014923,63,6.94E-67
1.10E-70,62,210,Mucopolysaccharidosis I,D008059,12,5.22E-67
3.06E-70,80,488,Abnormal behavior,D000066553,328,1.46E-66
1.54E-70,62,211,Myelodysplastic-Myeloproliferative Diseases,D054437,15,7.33E-67
2.16E-70,62,212,"PNEUMOTHORAX, PRIMARY SPONTANEOUS",C566795,13,1.03E-66
4.58E-70,65,251,Dyslexia,D004410,65,2.17E-66
9.31E-70,76,421,Hypothyroidism,D007037,242,4.42E-66
7.84E-70,66,266,Sudden infant death syndrome,D013398,73,3.72E-66
3.47E-70,61,202,Tracheobronchomalacia,D055089,3,1.65E-66
8.18E-70,62,216,Enchondroma,D002812,16,3.88E-66
2.44E-70,61,201,Teebi syndrome,C536951,1,1.16E-66
2.44E-70,61,201,"Dermatitis, Atopic, 2",C565293,1,1.16E-66
2.44E-70,61,201,"Hemorrhagic Fever, Argentinian",D006478,1,1.16E-66
2.44E-70,61,201,Oculomaxillofacial dysostosis,C537736,1,1.16E-66
2.44E-70,61,201,"HEMOCHROMATOSIS, TYPE 2B",C566557,1,1.16E-66
2.45E-69,77,444,Psychotic Disorders,D011618,287,1.16E-65
1.38E-69,61,206,Thoracic Outlet Syndrome,D013901,6,6.56E-66
4.02E-69,72,361,Muscular Dystrophy,D009136,181,1.91E-65
3.04E-69,60,197,Fecal Incontinence,D005242,7,1.44E-65
6.89E-69,66,274,Macroglossia,D008260,83,3.27E-65
8.64E-69,70,333,"Polycystic Kidney, Autosomal Dominant",D016891,143,4.09E-65
9.47E-69,71,349,Deglutition Disorders,D003680,180,4.49E-65
1.08E-68,68,304,Myotonic Dystrophy,D009223,112,5.11E-65
1.44E-68,61,213,"Familial Partial Lipodystrophy, Type 2",D052496,13,6.82E-65
3.96E-68,83,579,nervous system disorder,D009422,398,1.87E-64
3.09E-68,65,266,Pulmonary Embolism,D011655,71,1.46E-64
5.15E-68,74,407,Patent ductus arteriosus,D004374,232,2.43E-64
3.83E-68,61,216,Sick Sinus Syndrome,D012804,18,1.81E-64
8.63E-68,77,464,Peripheral Neuropathy,D010523,286,4.08E-64
2.44E-68,60,203,Myofibroblastoma,D009379,3,1.15E-64
2.44E-68,60,203,Clonorchiasis,D003003,3,1.15E-64
1.23E-68,60,201,"Autoimmune Lymphoproliferative Syndrome, Type IIA",C565833,1,5.81E-65
4.80E-68,60,205,SPLIT-HAND/FOOT MALFORMATION 4,C565344,5,2.27E-64
4.80E-68,60,205,RAPP-HODGKIN SYNDROME,C535289,5,2.27E-64
1.56E-67,66,286,Thrombosis,D013927,90,7.39E-64
1.31E-67,60,208,Dysmenorrhea,D004412,9,6.17E-64
1.82E-67,60,209,Cerebral Cavernous Malformations 3,C566393,11,8.58E-64
4.36E-67,63,249,Xerostomia,D014987,60,2.06E-63
7.47E-67,80,536,Adenomatous Polyposis Coli,D011125,362,3.52E-63
3.50E-67,60,211,Nesidioblastosis,D046768,12,1.65E-63
4.84E-67,60,212,Cardio-facio-cutaneous syndrome,C535579,13,2.28E-63
1.19E-66,64,266,Marfan Syndrome,D008382,69,5.58E-63
1.47E-66,66,295,Tetralogy of Fallot,D013771,113,6.93E-63
1.20E-66,61,227,Phenylketonurias,D010661,28,5.63E-63
8.38E-67,59,202,Malignant neoplasm of retina,D019572,2,3.95E-63
1.17E-66,59,203,"Vohwinkel Syndrome, Variant Form",C565826,3,5.52E-63
5.99E-67,59,201,Wieacker-Wolff syndrome,C536703,1,2.82E-63
5.99E-67,59,201,Hypermanganesemia with Dystonia Polycythemia and Cirrhosis,C548016,1,2.82E-63
5.99E-67,59,201,Androgen Receptor Deficiency,D013734,1,2.82E-63
5.99E-67,59,201,Type I familial incomplete male pseudohermaphroditism,C538435,1,2.82E-63
5.99E-67,59,201,"Spinal Muscular Atrophy, Distal, X-Linked 3",C564506,1,2.82E-63
5.99E-67,59,201,"ERYTHROCYTOSIS, FAMILIAL, 2",C563918,1,2.82E-63
5.99E-67,59,201,"Bulbospinal neuronopathy, X-linked recessive",C537017,1,2.82E-63
5.99E-67,59,201,"Genital Diseases, Male",D005832,1,2.82E-63
5.99E-67,59,201,KALLMANN SYNDROME 5 (disorder),C567220,1,2.82E-63
5.99E-67,59,201,"Maxillonasal dysplasia, Binder type",C536036,1,2.82E-63
4.37E-66,65,285,Pick Disease of the Brain,D020774,97,2.05E-62
3.26E-66,60,218,Familial generalized lipodystrophy,D052497,19,1.53E-62
2.28E-66,59,205,Vitamin D-resistant rickets,D063730,5,1.07E-62
3.16E-66,59,206,Factor XII Deficiency,D005175,8,1.49E-62
3.16E-66,59,206,Pili torti-deafness syndrome,C537633,7,1.49E-62
3.16E-66,59,206,"Histiocytosis, Non-Langerhans-Cell",D015616,6,1.49E-62
3.16E-66,59,206,Osteoglophonic dwarfism,C536050,6,1.49E-62
3.16E-66,59,206,Opticospinal Multiple Sclerosis,C580329,6,1.49E-62
4.39E-66,59,207,Neoplastic Processes,D009385,11,2.06E-62
1.69E-65,75,457,Fetal Growth Retardation,D005317,286,7.92E-62
1.16E-65,59,210,Asymmetric crying face association,C535349,14,5.43E-62
1.16E-65,59,210,Humoral hypercalcemia of malignancy (disorder),C562390,10,5.43E-62
2.31E-65,61,237,Osteosclerosis,D010026,43,1.08E-61
2.79E-65,60,225,Adult Learning Disorders,D007859,28,1.31E-61
2.83E-65,58,201,Achlorhydria,D000126,2,1.33E-61
7.66E-65,59,216,Cartilaginous exostosis,D015831,18,3.58E-61
3.94E-65,58,202,Aromatase deficiency,C537436,3,1.84E-61
3.94E-65,58,202,"Hypophosphatemic Rickets, Autosomal Recessive, 2",C567647,2,1.84E-61
5.46E-65,58,203,Rathke Cleft Cysts,D020863,3,2.56E-61
5.46E-65,58,203,Autosomal recessive hypophosphatemic vitamin D refractory rickets,C562792,3,2.56E-61
1.42E-64,59,218,Alcohol consumption,D000428,32,6.63E-61
2.83E-65,58,201,"Erythrocytosis, Familial, 4",C567086,1,1.33E-61
7.57E-65,58,204,Mydriasis,D015878,5,3.54E-61
7.57E-65,58,204,ADULT SYNDROME,C538052,4,3.54E-61
1.05E-64,58,205,Acrodermatitis enteropathica,C538178,6,4.90E-61
1.05E-64,58,205,Congenital glucose-galactose malabsorption,C562602,5,4.90E-61
1.92E-64,59,219,"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1",C537340,20,8.99E-61
1.44E-64,58,206,Central Nervous System Sensitization,D059333,6,6.75E-61
1.99E-64,58,207,Neurogenic Urinary Bladder,D001750,10,9.30E-61
2.74E-64,58,208,"Cystadenoma, Mucinous",D018291,10,1.28E-60
3.75E-64,58,209,Short Bowel Syndrome,D012778,9,1.75E-60
3.75E-64,58,209,Diabetes mellitus autosomal dominant type II (disorder),C564219,9,1.75E-60
5.14E-64,58,210,Skin callus,D002145,12,2.40E-60
5.14E-64,58,210,Abdominal obesity metabolic syndrome,C535554,11,2.40E-60
1.31E-63,58,213,Multiple System Atrophy,D019578,15,6.10E-60
2.42E-63,58,215,Acquired partial lipodystrophy,C562448,15,1.13E-59
4.09E-63,63,284,Nephrolithiasis,D053040,88,1.91E-59
1.30E-63,57,201,SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION,C564307,2,6.06E-60
1.79E-63,57,202,Alzheimer disease type 1,C536594,2,8.35E-60
1.79E-63,57,202,Li-Fraumeni Syndrome 2,C563755,2,8.35E-60
2.47E-63,57,203,Middle Ear Cholesteatoma,D018424,3,1.15E-59
1.30E-63,57,201,"Glutamine deficiency, congenital",C536832,1,6.06E-60
1.30E-63,57,201,"Conjunctivitis, Acute Hemorrhagic",D003232,1,6.06E-60
1.30E-63,57,201,PEHO-Like Syndrome,C536317,1,6.06E-60
3.40E-63,57,204,Nut Hypersensitivity,D021184,4,1.58E-59
3.40E-63,57,204,"MYOPATHY, CONGENITAL, WITH EXCESS OF MUSCLE SPINDLES",C566896,4,1.58E-59
4.67E-63,57,205,Adiponectin Deficiency,C567258,5,2.17E-59
6.40E-63,57,206,Female Pseudohermaphroditism,D058489,6,2.98E-59
6.40E-63,57,206,"Lipomatosis, Multiple Symmetrical",D008069,6,2.98E-59
6.40E-63,57,206,NADH cytochrome B5 reductase deficiency,C537841,6,2.98E-59
2.29E-62,98,1087,Parkinson Disease,D010300,941,1.06E-58
1.09E-62,58,220,Shared Paranoid Disorder,D012753,20,5.05E-59
8.75E-63,57,207,WHIM syndrome,C536697,7,4.07E-59
2.49E-62,60,249,Bradykinesia,D018476,56,1.16E-58
2.49E-62,60,249,Hyperandrogenism,D017588,53,1.16E-58
1.63E-62,57,209,Cataract microcornea syndrome,C538287,9,7.58E-59
1.63E-62,57,209,Angioid Streaks,D000793,9,7.58E-59
4.05E-62,74,485,Hypertrophic Cardiomyopathy,D002312,302,1.88E-58
2.22E-62,57,210,Lipoatrophic Diabetes Mellitus,D003923,10,1.03E-58
3.01E-62,57,211,Self Mutilation,D012652,16,1.40E-58
4.72E-62,59,238,"Obesity, Visceral",D056128,41,2.19E-58
4.08E-62,57,212,Thanatophoric Dysplasia,D013796,13,1.90E-58
7.47E-62,57,214,Anhidrosis,D007007,22,3.46E-58
2.27E-61,85,746,Autistic Disorder,D001321,603,1.05E-57
7.90E-62,56,202,Headache Disorders,D020773,3,3.66E-58
3.97E-61,72,460,Mental disorders,D001523,295,1.83E-57
7.90E-62,56,202,"Cataract, Zonular Pulverulent 1",C566158,2,3.66E-58
7.90E-62,56,202,"Hypoproteinemia, Hypercatabolic",C565476,2,3.66E-58
7.90E-62,56,202,"CHOANAL ATRESIA, POSTERIOR",C562435,2,3.66E-58
7.90E-62,56,202,Myofascial Pain Syndromes,D009209,2,3.66E-58
7.90E-62,56,202,Eye pain,D058447,2,3.66E-58
1.08E-61,56,203,Radiculopathy,D011843,3,5.01E-58
1.08E-61,56,203,Syringocystadenoma Papilliferum,D000074009,3,5.01E-58
1.08E-61,56,203,Familial Olivopontocerebellar Atrophy,D009849,3,5.01E-58
5.76E-62,56,201,"Cataract, Nuclear Diffuse Nonprogressive",C566157,1,2.67E-58
5.76E-62,56,201,Retinol Deficiency,C536156,1,2.67E-58
5.76E-62,56,201,Enterobacteriaceae Infections,D004756,1,2.67E-58
5.76E-62,56,201,Phosphoglycerate Dehydrogenase Deficiency,C566618,1,2.67E-58
1.48E-61,56,204,Megalanecephaly Polymicrogyria-Polydactyly Hydrocephalus Syndrome,C566381,4,6.84E-58
1.48E-61,56,204,GIANT PIGMENTED HAIRY NEVUS,C536819,4,6.84E-58
2.02E-61,56,205,"HEMIHYPERPLASIA, ISOLATED",C565524,7,9.33E-58
2.02E-61,56,205,"Cataract, Central Saccular, With Sutural Opacities",C565301,5,9.33E-58
2.75E-61,56,206,NOONAN SYNDROME 3,C537847,6,1.27E-57
4.39E-61,57,220,Lipomatosis,D008068,21,2.03E-57
3.73E-61,56,207,BIETTI CRYSTALLINE CORNEORETINAL DYSTROPHY,C535440,8,1.72E-57
5.06E-61,56,208,"Fibromatosis, Gingival",D005351,12,2.34E-57
6.86E-61,56,209,"Cataract, Pulverulent",C563426,9,3.16E-57
4.27E-60,57,228,Gingival Hypertrophy,D005886,46,1.96E-56
3.04E-60,56,214,"DIABETES MELLITUS, PERMANENT NEONATAL",C563425,14,1.40E-56
4.08E-60,56,215,"Dystonia, Diurnal",D004421,17,1.87E-56
2.48E-60,55,201,Familial Hypertrophic Cardiomyopathy Type 4,C566169,2,1.14E-56
7.30E-60,56,217,Epidermolysis Bullosa Acquisita,D016107,18,3.34E-56
1.63E-59,79,636,Cataract,D002386,477,7.46E-56
1.58E-59,69,425,Congenital Heart Defects,D006330,256,7.22E-56
4.59E-60,55,203,Hereditary Sensory Radicular Neuropathy,D009477,4,2.11E-56
3.38E-60,55,202,"Scotoma, Ring",D012607,2,1.55E-56
3.38E-60,55,202,Juvenile Xanthogranuloma,D014972,2,1.55E-56
3.38E-60,55,202,"Atrial Septal Defect, Secundum Type",C566241,2,1.55E-56
3.38E-60,55,202,Phosphoenolpyruvate carboxykinase deficiency,C536654,2,1.55E-56
3.38E-60,55,202,Noonan-Like Syndrome With Loose Anagen Hair,C564342,2,1.55E-56
4.59E-60,55,203,"Hepatitis, Animal",D006520,3,2.11E-56
4.59E-60,55,203,Myofibroma (morphologic abnormality),D047708,3,2.11E-56
4.59E-60,55,203,Metachondromatosis,C562938,3,2.11E-56
4.59E-60,55,203,Root Resorption,D012391,3,2.11E-56
6.24E-60,55,204,"Granular Dystrophy, Corneal",D003317,5,2.85E-56
6.24E-60,55,204,Hypopharyngeal Cancer,D007012,5,2.85E-56
2.48E-60,55,201,"CATARACT, POSTERIOR POLAR, 4 (disorder)",C535344,1,1.14E-56
2.48E-60,55,201,"Cataract, Posterior Polar, 2",C565134,1,1.14E-56
2.48E-60,55,201,Hutchinson's Melanotic Freckle,D018327,1,1.14E-56
2.48E-60,55,201,"CATARACT, CONGENITAL, CERULEAN TYPE, 3",C563819,1,1.14E-56
2.48E-60,55,201,Legionellosis,D007876,1,1.14E-56
2.48E-60,55,201,Aphakia,D001035,1,1.14E-56
2.48E-60,55,201,Neoplasm Seeding,D009366,1,1.14E-56
2.48E-60,55,201,Phosphoenolpyruvate carboxykinase 2 deficiency,C536655,1,1.14E-56
2.48E-60,55,201,"Cataract, Autosomal Dominant, Multiple Types 1",C566909,1,1.14E-56
2.48E-60,55,201,"Cataracts, Congenital, with Sensorineural Deafness, Down Syndrome-Like Facial Appearance, Short Stature, and Mental Retardation",C563390,1,1.14E-56
2.48E-60,55,201,"Cataract, Congenital Zonular, with Sutural Opacities",C563435,1,1.14E-56
2.48E-60,55,201,Noonan Syndrome 4,C548082,1,1.14E-56
2.48E-60,55,201,"Cataract, Congenital, Cerulean Type, 2",C563294,1,1.14E-56
2.48E-60,55,201,Craniofacial Pain,D005157,1,1.14E-56
2.48E-60,55,201,Hashimoto-Pritzker syndrome,C535843,1,1.14E-56
2.48E-60,55,201,Alpha-B Crystallinopathy,C563848,1,1.14E-56
2.48E-60,55,201,"Cataract, Punctate, Progressive Juvenile-Onset",C565131,1,1.14E-56
2.48E-60,55,201,"Cataract, Congenital Nuclear, Autosomal Recessive 2",C565725,1,1.14E-56
2.48E-60,55,201,"Cataract, Zonular Pulverulent 3",C566608,1,1.14E-56
2.48E-60,55,201,"Cataract, Pulverulent, Juvenile-Onset",C565703,1,1.14E-56
2.48E-60,55,201,"Cataract, Cortical, Juvenile-Onset",C566955,1,1.14E-56
2.48E-60,55,201,"Cataract, Autosomal Recessive Congenital 1",C565136,1,1.14E-56
2.48E-60,55,201,"CATARACT, CRYSTALLINE ACULEIFORM",C566162,1,1.14E-56
6.24E-60,55,204,Familial expansile osteolysis,C536335,4,2.85E-56
6.24E-60,55,204,"Cataract, congenital, cerulean type 1",C537955,4,2.85E-56
6.24E-60,55,204,Monckeberg Medial Calcific Sclerosis,D050380,4,2.85E-56
1.14E-59,55,206,Renal Osteodystrophy,D012080,7,5.22E-56
1.14E-59,55,206,Spondylolysis,D013169,7,5.22E-56
1.14E-59,55,206,Erdheim-Chester Disease,D031249,7,5.22E-56
2.21E-59,57,234,Aortic coarctation,D001017,43,1.01E-55
2.08E-59,55,208,Lacrimal Duct Obstruction,D007767,10,9.49E-56
3.76E-59,55,210,Pulmonary Valve Stenosis,D011666,12,1.71E-55
3.76E-59,55,210,"NEVUS, EPIDERMAL (disorder)",C580062,11,1.71E-55
5.04E-59,55,211,Skin Manifestations,D012877,13,2.30E-55
9.24E-59,56,226,Delusions,D003702,31,4.21E-55
9.24E-59,56,226,Activated Protein C Resistance,D020016,28,4.21E-55
9.01E-59,55,213,Cleidocranial Dysplasia,D002973,16,4.11E-55
1.20E-58,55,214,Rare Diseases,D035583,20,5.48E-55
2.10E-58,56,229,Coffin-Siris syndrome,C536436,33,9.53E-55
1.40E-58,54,202,"CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT (disorder)",C567275,3,6.37E-55
1.40E-58,54,202,Craniodiaphyseal dysplasia,C562940,3,6.37E-55
1.89E-58,54,203,Myopathy with Abnormal Lipid Metabolism,C562935,4,8.60E-55
1.40E-58,54,202,"Striatal Degeneration, Autosomal Dominant",C563783,2,6.37E-55
1.40E-58,54,202,Monosomy 7 of Bone Marrow,C565370,2,6.37E-55
1.40E-58,54,202,Dental Calculus,D003728,2,6.37E-55
1.40E-58,54,202,Parotitis,D010309,2,6.37E-55
1.89E-58,54,203,Acanthoma,D049309,3,8.60E-55
1.89E-58,54,203,Linear Verrucous Epidermal Nevus,D054000,3,8.60E-55
1.89E-58,54,203,Eccrine acrospiroma,D018250,3,8.60E-55
1.89E-58,54,203,Pigeon Breeder's Lung,D001716,3,8.60E-55
3.43E-58,54,205,Ankyloglossia,D000072676,9,1.56E-54
1.03E-58,54,201,Tick-Borne Diseases,D017282,1,4.71E-55
1.03E-58,54,201,Carotid Intimal Medial Thickness 1,C563733,1,4.71E-55
2.55E-58,54,204,Thinness,D013851,4,1.16E-54
4.61E-58,54,206,Lymphedema praecox,C562467,6,2.09E-54
6.18E-58,54,207,"MENTAL RETARDATION, X-LINKED, SNYDER-ROBINSON TYPE",C536678,7,2.80E-54
8.27E-58,54,208,Alacrima,C562827,10,3.75E-54
1.11E-57,54,209,SHORT syndrome,C537327,9,5.02E-54
1.47E-57,54,210,Hypochondroplasia (disorder),C562937,13,6.69E-54
1.47E-57,54,210,Strudwick syndrome,C537501,12,6.69E-54
3.39E-57,55,226,Gingival Hyperplasia,D005885,45,1.54E-53
2.30E-57,53,199,APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS,C563969,2,1.04E-53
7.53E-57,53,203,Scimitar Syndrome,D012587,8,3.40E-53
7.53E-57,53,203,Hearing problem,D006311,6,3.40E-53
7.53E-57,53,203,"HEMANGIOMA, CAPILLARY INFANTILE",C535860,4,3.40E-53
7.53E-57,53,203,Oncogene Addiction,D000074723,4,3.40E-53
5.61E-57,53,202,JACKSON-WEISS SYNDROME,C537559,2,2.54E-53
5.61E-57,53,202,Pfeiffer type acrocephalosyndactyly,C538582,2,2.54E-53
5.61E-57,53,202,TYPHUS,D014438,2,2.54E-53
5.61E-57,53,202,Uhl anomaly,C536932,2,2.54E-53
5.61E-57,53,202,Muenke Syndrome,C537369,2,2.54E-53
5.61E-57,53,202,"Bone Diseases, Endocrine",D001849,2,2.54E-53
5.61E-57,53,202,Stomatognathic Diseases,D009057,2,2.54E-53
5.61E-57,53,202,Dermatosis Papulosa Nigra,C562379,2,2.54E-53
5.61E-57,53,202,Pseudarthrosis,D011542,2,2.54E-53
1.01E-56,53,204,"Lacrimal Puncta, Absence of",C566703,6,4.55E-53
7.53E-57,53,203,Lacrimoauriculodentodigital syndrome,C538132,3,3.40E-53
7.53E-57,53,203,Corneal Perforation,D057112,3,3.40E-53
7.53E-57,53,203,Intussusception,D007443,3,3.40E-53
4.18E-57,53,201,Otodental Dysplasia,C563482,1,1.89E-53
4.18E-57,53,201,LEOPARD SYNDROME 2,C537117,1,1.89E-53
4.18E-57,53,201,Bilateral Nasal Obstruction,D015508,1,1.89E-53
4.18E-57,53,201,Phacomatosis pigmentokeratotica,C537893,1,1.89E-53
4.18E-57,53,201,"Adrenal Hypoplasia, Cytomegalic Type",C564543,1,1.89E-53
4.18E-57,53,201,Aplasia of Lacrimal and Salivary Glands,C562407,1,1.89E-53
4.18E-57,53,201,Noonan Syndrome 5,C548083,1,1.89E-53
4.18E-57,53,201,Age-Related Macular Degeneration type 11,C567450,1,1.89E-53
4.18E-57,53,201,METACARPAL 4-5 FUSION,C564100,1,1.89E-53
1.01E-56,53,204,Dacryocystitis,D003607,4,4.55E-53
1.01E-56,53,204,Hepatic Insufficiency,D048550,4,4.55E-53
1.35E-56,53,205,Lymphangiectasis,D008200,5,6.07E-53
1.35E-56,53,205,Proctitis,D011349,5,6.07E-53
1.35E-56,53,205,Heterotopic Ossification,D009999,5,6.07E-53
2.80E-56,55,234,Corneal Neovascularization,D016510,39,1.26E-52
2.42E-56,54,220,Hyperphosphatemia (disorder),D054559,23,1.09E-52
1.80E-56,53,206,Donohue Syndrome,D056731,9,8.10E-53
1.80E-56,53,206,Ramer Ladda syndrome,C535284,8,8.10E-53
3.64E-56,56,249,"Epilepsy, Cryptogenic",D004827,59,1.64E-52
2.40E-56,53,207,Multiple Endocrine Neoplasia Type 2b,D018814,9,1.08E-52
2.40E-56,53,207,"Atrophy, Disuse",D020966,7,1.08E-52
2.40E-56,53,207,Polyostotic fibrous dysplasia,D005359,7,1.08E-52
4.16E-56,54,222,Endemic Cretinism,D003409,22,1.87E-52
4.23E-56,53,209,"Dystonia 3, Torsion, X-Linked",C564048,11,1.90E-52
4.23E-56,53,209,Hypothalamic hamartomas,C537158,9,1.90E-52
4.23E-56,53,209,Lentigo,D007911,9,1.90E-52
4.23E-56,53,209,Bronchomalacia,D055091,9,1.90E-52
1.32E-55,57,269,Maturity onset diabetes mellitus in young,C562772,73,5.91E-52
1.29E-55,55,240,Action Tremor,D014202,51,5.79E-52
1.66E-55,57,270,"Muscular Dystrophy, Facioscapulohumeral",D020391,82,7.42E-52
9.82E-56,53,212,Coffin-Lowry syndrome,D038921,12,4.41E-52
1.57E-55,54,227,TUBEROUS SCLEROSIS 2 (disorder),C566021,27,7.04E-52
2.25E-55,53,215,Blepharospasm,D001764,16,1.00E-51
1.63E-55,52,201,Talipes cavus,D000070589,3,7.33E-52
6.39E-55,56,261,Hematocrit procedure,D006400,92,2.86E-51
2.18E-55,52,202,Unerupted tooth,D014097,3,9.76E-52
5.07E-55,53,218,Port-Wine Stain,D019339,20,2.27E-51
2.18E-55,52,202,Neutral Lipid Storage Disease with Myopathy,C565192,2,9.76E-52
2.18E-55,52,202,"Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia",C565195,2,9.76E-52
2.90E-55,52,203,Fetal Macrosomia,D005320,3,1.30E-51
6.62E-55,53,219,Vascular anomaly,D054079,20,2.96E-51
6.62E-55,53,219,TDP-43 Proteinopathies,D057177,20,2.96E-51
1.63E-55,52,201,CHAR SYNDROME,C566815,1,7.33E-52
1.63E-55,52,201,"Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip-Palate",C564484,1,7.33E-52
1.63E-55,52,201,Ecthyma,D004473,1,7.33E-52
1.63E-55,52,201,Atrial Septal Defect Sinus Venosus,C548009,1,7.33E-52
1.63E-55,52,201,Paratubal Cyst,D010310,1,7.33E-52
1.63E-55,52,201,SCALP-EAR-NIPPLE SYNDROME,C536623,1,7.33E-52
3.86E-55,52,204,Isolated hypoplasia of the right ventricle,C535682,4,1.73E-51
5.13E-55,52,205,THROMBOCYTOPENIA 2 (disorder),C536519,7,2.29E-51
6.80E-55,52,206,"EPILEPSY, PYRIDOXINE-DEPENDENT",C536254,9,3.04E-51
6.80E-55,52,206,Spondylolisthesis,D013168,8,3.04E-51
1.57E-54,52,209,Sotos' syndrome,D058495,10,7.01E-51
2.07E-54,52,210,Aplasia/Hypoplasia of the thumb,C536903,12,9.23E-51
2.72E-54,52,211,Wolf-Hirschhorn Syndrome,D054877,14,1.21E-50
3.57E-54,52,212,"Histiocytoma, Angiomatoid Fibrous",C563181,12,1.59E-50
8.02E-54,52,215,Plagiocephaly,D059041,23,3.57E-50
8.02E-54,52,215,"Plagiocephaly, Nonsynostotic",D049068,23,3.57E-50
8.02E-54,52,215,Anti-Glomerular Basement Membrane Disease,D019867,17,3.57E-50
1.15E-53,53,230,Macrocephaly,D058627,36,5.14E-50
8.20E-54,51,202,"Macular Dystrophy, Butterfly-Shaped Pigmentary, 2",C536309,3,3.65E-50
8.20E-54,51,202,Antley-Bixler Syndrome Phenotype,D054882,2,3.65E-50
8.20E-54,51,202,Butyrylcholinesterase deficiency,C537417,2,3.65E-50
6.18E-54,51,201,Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia,C567466,1,2.76E-50
6.18E-54,51,201,"SCAPHOCEPHALY, MAXILLARY RETRUSION, AND MENTAL RETARDATION",C566511,1,2.76E-50
6.18E-54,51,201,Cutis Gyrata Syndrome of Beare And Stevenson,C565129,1,2.76E-50
6.18E-54,51,201,Vogt Cephalodactyly,C566327,1,2.76E-50
6.18E-54,51,201,"Obesity, Hyperphagia, and Developmental Delay",C563938,1,2.76E-50
4.01E-53,53,235,Arrhythmogenic Right Ventricular Dysplasia,D019571,36,1.79E-49
3.45E-52,76,709,Congenital Abnormality,D000013,549,1.53E-48
1.64E-52,51,213,"Hearing Loss, Mixed Conductive-Sensorineural",D046089,16,7.30E-49
3.60E-52,51,216,Hypotrichosis simplex,C537160,21,1.60E-48
6.16E-52,52,232,Facial asymmetry,D005146,43,2.74E-48
3.92E-52,50,203,Ankyloblepharon filiforme adnatum,C536373,4,1.74E-48
7.79E-52,51,219,Oligomenorrhea,D009839,20,3.46E-48
2.98E-52,50,202,Ventral Hernia,D006555,2,1.32E-48
1.01E-51,51,220,Protein C Deficiency,D020151,26,4.46E-48
5.15E-52,50,204,Uterine Prolapse,D014596,4,2.29E-48
2.26E-52,50,201,Placenta Accreta,D010921,1,1.01E-48
2.26E-52,50,201,"VENOUS MALFORMATIONS, MULTIPLE CUTANEOUS AND MUCOSAL",C563977,1,1.01E-48
2.26E-52,50,201,Blue rubber bleb nevus syndrome,C536240,1,1.01E-48
2.26E-52,50,201,Mitochondrial myopathy with lactic acidosis,C537476,1,1.01E-48
1.67E-51,51,222,von Willebrand Disease,D014842,25,7.39E-48
1.15E-51,50,207,Cat eye syndrome,C535918,7,5.12E-48
1.51E-51,50,208,Fanconi-Bickel Syndrome,D005198,10,6.67E-48
1.51E-51,50,208,Urologic Diseases,D014570,9,6.67E-48
1.51E-51,50,208,Intestinal Atresia,D007409,9,6.67E-48
3.31E-51,50,211,Hemarthrosis,D006395,11,1.47E-47
6.68E-51,52,242,Hypophosphatemia,D017674,49,2.96E-47
9.29E-51,50,215,Ketonuria,D007662,18,4.11E-47
1.20E-50,50,216,Thromboembolism,D013923,17,5.30E-47
1.37E-50,49,203,"Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration",C564603,7,6.06E-47
2.45E-50,51,233,Disseminated Intravascular Coagulation,D004211,38,1.08E-46
1.05E-50,49,202,Bifid Nose With Or Without Anorectal And Renal Anomalies,C567672,2,4.65E-47
1.05E-50,49,202,Cronkhite-Canada Syndrome,D044483,2,4.65E-47
1.37E-50,49,203,22q13.3 Deletion Syndrome,C536801,3,6.06E-47
1.37E-50,49,203,"Osteogenesis Imperfecta, Type VI",C536047,3,6.06E-47
1.37E-50,49,203,Oculopharyngodistal Myopathy,C563508,3,6.06E-47
1.79E-50,49,204,"Maturity-Onset Diabetes of the Young, Type 1",C565101,4,7.90E-47
8.02E-51,49,201,Alzheimer Disease 12,C567022,1,3.55E-47
8.02E-51,49,201,"Cerebellar degeneration, subacute",C535352,1,3.55E-47
3.93E-50,49,207,"Total Hypotrichosis, Mari type",C536973,7,1.74E-46
6.84E-50,50,223,Hemophilia B,D002836,35,3.02E-46
8.06E-50,52,253,Williams Syndrome,D018980,59,3.56E-46
1.41E-49,50,226,Congenital Hyperinsulinism,D044903,26,6.24E-46
1.98E-49,51,242,Epistaxis,D004844,46,8.74E-46
2.61E-49,55,307,Exophthalmos,D005094,130,1.15E-45
5.64E-49,52,262,Venous Thromboembolism,D054556,75,2.49E-45
6.32E-49,49,218,"Angioedemas, Hereditary",D054179,19,2.78E-45
9.31E-49,50,234,Thrombasthenia,D013915,40,4.10E-45
8.07E-49,49,219,Protein S Deficiency,D018455,23,3.55E-45
6.01E-49,48,204,Methylmalonic acidemia with homocystinuria,C537359,6,2.65E-45
4.64E-49,48,203,Poroma,D057091,3,2.04E-45
2.75E-49,48,201,"CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL",C563463,1,1.21E-45
2.75E-49,48,201,"Memory, Episodic",D061212,1,1.21E-45
2.75E-49,48,201,"CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE",C563462,1,1.21E-45
2.75E-49,48,201,"CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LATE-ONSET",C563461,1,1.21E-45
1.67E-48,49,222,Goiter,D006042,23,7.33E-45
2.43E-48,52,269,Thrombophilia,D019851,73,1.07E-44
1.67E-48,48,208,Cerebral Thrombosis,D020767,8,7.35E-45
2.15E-48,48,209,"Thrombophilia, hereditary",C540694,10,9.45E-45
3.54E-48,48,211,Afibrinogenemia,D000347,14,1.56E-44
4.53E-48,48,212,Budd-Chiari Syndrome,D006502,13,1.99E-44
1.20E-47,48,216,Gingival Hemorrhage,D005884,19,5.29E-44
2.16E-47,49,233,Hypoalbuminemia,D034141,41,9.48E-44
1.95E-47,47,204,Hepatoblastoma Caused By Somatic Mutation,C567299,5,8.58E-44
2.51E-47,47,205,Hereditary Factor V Deficiency,D005166,5,1.10E-43
2.51E-47,47,205,Familial neurocardiogenic syncope,C536849,5,1.10E-43
2.51E-47,47,205,"Dysfibrinogenemia, Congenital",C562727,5,1.10E-43
1.18E-46,68,625,"Genetic Diseases, Inborn",D030342,474,5.20E-43
5.29E-47,47,208,Rectovaginal Fistula,D012006,9,2.32E-43
2.20E-46,54,327,Premature Menopause,D008594,138,9.64E-43
2.65E-46,52,293,Hirschsprung Disease,D006627,110,1.16E-42
2.87E-46,47,215,Tracheomalacia,D055090,18,1.26E-42
3.75E-46,46,202,Diabetes-deafness syndrome maternally transmitted (disorder),C536246,2,1.64E-42
4.80E-46,46,203,Sagittal Sinus Thrombophlebitis,D020225,3,2.10E-42
4.80E-46,46,203,Splenic Rupture,D013161,3,2.10E-42
4.80E-46,46,203,Hereditary Factor XIII Deficiency,D005177,3,2.10E-42
4.80E-46,46,203,"Embolism, Paradoxical",D019320,3,2.10E-42
4.80E-46,46,203,"Hypodysfibrinogenemia, Congenital",C565970,3,2.10E-42
4.80E-46,46,203,Mesenteric Vascular Occlusion,D008641,3,2.10E-42
1.59E-45,50,269,Telecanthus,C562941,90,6.93E-42
7.84E-46,46,205,"Abortion, Habitual",D000026,6,3.43E-42
2.92E-46,46,201,Peliosis Hepatis,D010382,1,1.28E-42
2.92E-46,46,201,"NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIB",C567084,1,1.28E-42
1.00E-45,46,206,"Diabetes Mellitus, Transient Neonatal, 1",C563322,9,4.37E-42
7.84E-46,46,205,"Blood Coagulation Disorders, Inherited",D025861,5,3.43E-42
1.27E-45,46,207,Purpura Fulminans,D055665,11,5.57E-42
1.62E-45,46,208,Nose Diseases,D009668,8,7.08E-42
2.61E-45,46,210,Arachnoid Cysts,D016080,15,1.14E-41
7.00E-45,47,229,Thrombotic Microangiopathies,D057049,31,3.06E-41
1.09E-44,53,332,Blood Coagulation Disorders,D001778,157,4.77E-41
1.22E-44,48,247,Cutis Laxa,D003483,55,5.30E-41
1.15E-44,45,202,Hereditary Antithrombin Deficiency,D020152,3,5.03E-41
1.47E-44,45,203,Hypoplasminogenemia,C580017,4,6.39E-41
1.15E-44,45,202,Central Nervous System Vascular Malformations,D020785,2,5.03E-41
1.15E-44,45,202,Postphlebitic Syndrome,D011186,2,5.03E-41
1.15E-44,45,202,ALPHA-2-PLASMIN INHIBITOR DEFICIENCY,C537777,2,5.03E-41
1.15E-44,45,202,Nonocclusive Mesenteric Ischemia,D065666,2,5.03E-41
1.86E-44,45,204,Transient erythroblastopenia of childhood,C536980,4,8.12E-41
2.37E-44,45,205,"Sinus Thrombosis, Intracranial",D012851,6,1.03E-40
3.00E-44,45,206,Premature ventricular contractions,D018879,9,1.31E-40
9.04E-45,45,201,MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY,C535706,1,3.94E-41
3.00E-44,45,206,Frontometaphyseal dysplasia,C538064,6,1.31E-40
3.80E-44,45,207,Activated Partial Thromboplastin Time measurement,D010314,9,1.65E-40
1.82E-44,44,190,"MATURITY-ONSET DIABETES OF THE YOUNG, TYPE IV (disorder)",C563451,2,7.95E-41
4.80E-44,45,208,"Thyroid cancer, follicular",C572845,8,2.09E-40
6.06E-44,45,209,Hereditary Factor XI Deficiency,D005173,9,2.64E-40
5.82E-43,45,219,Bernard-Soulier Syndrome,D001606,22,2.53E-39
3.42E-43,44,202,Porokeratosis,D017499,2,1.49E-39
3.42E-43,44,202,Inherited Factor II deficiency,D007020,2,1.49E-39
6.89E-43,44,205,X-linked agammaglobulinemia with growth hormone deficiency,C537149,8,2.99E-39
6.89E-43,44,205,"Amyloidosis, familial visceral",C538249,5,2.99E-39
2.70E-43,44,201,"Arterial Occlusive Disease, Progressive, with Hypertension, Heart Defects, Bone Fragility, and Brachysyndactyly",C566529,1,1.17E-39
2.70E-43,44,201,"Lymphoproliferative Syndrome, Ebv-Associated, Autosomal, 1",C567815,1,1.17E-39
4.22E-42,44,213,SEBASTIAN SYNDROME,C535507,13,1.83E-38
2.39E-41,44,221,Megacolon,D008531,30,1.03E-37
9.81E-42,43,202,"Epidermolysis Bullosa Dystrophica, Autosomal Recessive, Localisata Variant",C567121,3,4.25E-38
9.81E-42,43,202,"Hydatidiform Mole, Invasive",D002820,3,4.25E-38
9.81E-42,43,202,"Epidermolysis Bullosa Dystrophica Inversa, Autosomal Recessive",C567122,3,4.25E-38
6.75E-41,130,3533,Carcinogenesis,D063646,3427,2.92E-37
9.81E-42,43,202,Epididymitis,D004823,2,4.25E-38
9.81E-42,43,202,Pityriasis Rosea,D017515,2,4.25E-38
9.81E-42,43,202,Polymorphic Reticulosis,D006103,2,4.25E-38
2.43E-41,43,206,Potassium aggravated myotonia,C538353,8,1.05E-37
7.79E-42,43,201,"DEAFNESS, AUTOSOMAL RECESSIVE 39 (disorder)",C564265,1,3.38E-38
7.79E-42,43,201,Thrombophilia Due To Elevated Histidine-Rich Glycoprotein,C567737,1,3.38E-38
7.79E-42,43,201,"Wounds, Penetrating",D014950,1,3.38E-38
5.17E-41,47,274,Low Birth Weights,D007230,86,2.24E-37
2.43E-41,43,206,"VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1",C564741,7,1.05E-37
5.89E-41,43,210,"Pneumonia, Ventilator-Associated",D053717,11,2.55E-37
5.89E-41,43,210,Salaam Seizures,D013036,11,2.55E-37
5.89E-41,43,210,Angioedema,D000799,11,2.55E-37
7.33E-41,43,211,TUBEROUS SCLEROSIS 1 (disorder),C565346,12,3.17E-37
9.11E-41,43,212,Gastroschisis,D020139,14,3.94E-37
4.04E-40,43,219,Menorrhagia,D008595,20,1.74E-36
2.71E-40,42,202,Riboflavin Deficiency,D012257,4,1.17E-36
3.39E-40,42,203,"von Willebrand Disease, Type 2",D056728,4,1.46E-36
4.23E-40,42,204,Congenital atresia of pulmonary valve,D018633,5,1.82E-36
6.55E-40,42,206,"Erythroblastosis, Fetal",D004899,14,2.82E-36
3.39E-40,42,203,Hereditary factor II deficiency disease,C562724,3,1.46E-36
3.39E-40,42,203,Congenital abnormality of respiratory system,D015619,3,1.46E-36
3.39E-40,42,203,"PROPERDIN DEFICIENCY, X-LINKED",C537241,3,1.46E-36
3.39E-40,42,203,Acquired angioedema,C538173,3,1.46E-36
2.71E-40,42,202,Complement Component 4a Deficiency,C565167,2,1.17E-36
5.27E-40,42,205,Deficiency of butyryl-CoA dehydrogenase,C537596,6,2.27E-36
5.27E-40,42,205,Factor X Deficiency,D005171,5,2.27E-36
2.17E-40,42,201,Metaphyseal chondrodysplasia Spahr type,C537353,1,9.38E-37
2.17E-40,42,201,alpha-2-Macroglobulin Deficiency,C566304,1,9.38E-37
2.17E-40,42,201,Metaphyseal Anadysplasia 1,C567545,1,9.38E-37
2.17E-40,42,201,"Spondyloepimetaphyseal Dysplasia, Missouri Type",C566574,1,9.38E-37
6.55E-40,42,206,Congenital porencephaly,D065708,7,2.82E-36
8.14E-40,42,207,"Agammaglobulinemia, non-Bruton type",C538056,7,3.51E-36
1.01E-39,42,208,"WAARDENBURG SYNDROME, TYPE 4A",C536467,8,4.35E-36
2.37E-39,42,212,Vitamin K Deficiency,D014813,14,1.02E-35
3.75E-39,43,230,Pelvic Organ Prolapse,D056887,33,1.61E-35
3.61E-39,42,214,Primary amyloidosis,D000075363,17,1.55E-35
5.56E-39,43,232,"Glomerulonephritis, Membranoproliferative",D015432,34,2.39E-35
8.99E-39,41,203,Impetigo,D007169,5,3.86E-35
8.99E-39,41,203,"Cataract, total congenital with posterior sutural opacities in Heterozygotes",C535338,4,3.86E-35
8.99E-39,41,203,Thrombophlebitis,D013924,3,3.86E-35
7.24E-39,41,202,Dyserythropoietic Anemia with Thrombocytopenia,C564525,2,3.11E-35
1.71E-38,41,206,"CEROID LIPOFUSCINOSIS, NEURONAL, 6",C566627,9,7.32E-35
1.71E-38,41,206,Factor VII Deficiency,D005168,7,7.32E-35
1.71E-38,41,206,"Lactose Intolerance, Adult Type",C562601,7,7.32E-35
5.83E-39,41,201,Rocky Mountain Spotted Fever,D012373,1,2.51E-35
5.83E-39,41,201,"Thrombophilia, X-Linked, Due To Factor Ix Defect",C567581,1,2.51E-35
5.83E-39,41,201,Chromosome 4q- Syndrome,C537639,1,2.51E-35
5.83E-39,41,201,Aromatic amino acid decarboxylase deficiency,C537437,1,2.51E-35
5.83E-39,41,201,Glossalgia,D005926,1,2.51E-35
2.60E-38,41,208,Pressure Ulcer,D003668,8,1.11E-34
1.07E-37,42,231,Vertical Talus,D005413,37,4.58E-34
1.34E-37,41,216,Neonatal Alloimmune Thrombocytopenia,D054098,18,5.74E-34
3.60E-37,41,221,Ostium secundum atrial septal defect,D006344,22,1.54E-33
2.30E-37,40,203,External Carotid Artery Thrombosis,D002341,3,9.82E-34
1.86E-37,40,202,Toxic effect of carbon tetrachloride,D002252,2,7.97E-34
1.86E-37,40,202,Focal Infection,D005490,2,7.97E-34
2.83E-37,40,204,Arteritis,D001167,4,1.21E-33
1.51E-37,40,201,Flea Infestation,D058267,1,6.46E-34
1.51E-37,40,201,Petty Laxova Wiedemann syndrome,C537886,1,6.46E-34
1.51E-37,40,201,Metaphyseal Anadysplasia 2,C567771,1,6.46E-34
1.51E-37,40,201,"Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi",C567863,1,6.46E-34
1.51E-37,40,201,"Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay",C567769,1,6.46E-34
1.51E-37,40,201,Macrodactyly of the foot,C537719,1,6.46E-34
1.51E-37,40,201,Gorlin Chaudhry Moss syndrome,C537290,1,6.46E-34
1.51E-37,40,201,Antibody Deficiency due to Defect in CD19,C566275,1,6.46E-34
5.26E-37,40,207,CONOTRUNCAL HEART MALFORMATIONS (disorder),C535464,7,2.25E-33
6.45E-37,40,208,"Aneurysm, Ruptured",D017542,8,2.75E-33
1.44E-36,40,212,Urinary Stress Incontinence,D014550,13,6.16E-33
1.76E-36,40,213,Mouth Abnormalities,D009056,17,7.51E-33
2.14E-36,40,214,Hemangioendothelioma,D006390,14,9.14E-33
1.00E-35,40,222,Urogenital Abnormalities,D014564,25,4.25E-32
4.62E-36,39,202,POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY,C536329,3,1.97E-32
3.76E-36,39,201,Cranial nerve diseases,D003389,2,1.61E-32
8.48E-36,39,205,"von Willebrand Disease, Type 3",D056729,8,3.60E-32
1.87E-35,42,260,Diastolic blood pressure,D001794,100,7.92E-32
5.66E-36,39,203,Common atrioventricular canal,C535974,3,2.41E-32
5.66E-36,39,203,Agnosia,D000377,3,2.41E-32
5.66E-36,39,203,Pasteurellaceae Infections,D016871,3,2.41E-32
5.66E-36,39,203,"Bernard-Soulier Syndrome, Type B",C565549,3,2.41E-32
5.66E-36,39,203,"Bernard-Soulier Syndrome, Type C",C565550,3,2.41E-32
4.62E-36,39,202,"Craniosynostosis, Philadelphia Type",C563368,2,1.97E-32
4.62E-36,39,202,Cerebral Embolism and Thrombosis,D002542,2,1.97E-32
4.62E-36,39,202,Cholesterol Embolism,D017700,2,1.97E-32
4.62E-36,39,202,Hereditary Angioedema Type III,D056828,2,1.97E-32
4.62E-36,39,202,Monoparesis,D010291,2,1.97E-32
4.62E-36,39,202,High molecular weight kininogen deficiency,C537060,2,1.97E-32
6.94E-36,39,204,Hypotonia-Cystinuria Syndrome,C564710,4,2.95E-32
3.76E-36,39,201,"HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 5 (disorder)",C567123,1,1.61E-32
3.76E-36,39,201,Choroiditis,D002833,1,1.61E-32
3.76E-36,39,201,Atrial Septal Defect with Atrioventricular Conduction Defects,C566238,1,1.61E-32
3.76E-36,39,201,Granulomatous Mastitis,D058890,1,1.61E-32
3.76E-36,39,201,"Graft Occlusion, Vascular",D006083,1,1.61E-32
3.76E-36,39,201,"Heart Rupture, Post-Infarction",D006342,1,1.61E-32
2.28E-35,39,210,"von Willebrand Disease, Type 1",D056725,12,9.69E-32
4.95E-35,39,214,Diastrophic dysplasia,C536170,17,2.10E-31
7.41E-35,38,200,Platelet alpha-Granule Deficiency,D055652,2,3.14E-31
1.34E-34,38,203,"Hallucinations, Auditory",D006212,6,5.67E-31
1.10E-34,38,202,"Gallbladder, Agenesis Of",C562564,3,4.66E-31
9.04E-35,38,201,"Platelet Aggregation, Spontaneous",C566800,2,3.83E-31
9.04E-35,38,201,"Growth retardation, Alopecia, Pseudoanodontia and Optic atrophy",C535642,2,3.83E-31
1.34E-34,38,203,3-Hydroxyacyl-CoA Dehydrogenase Deficiency,C535310,4,5.67E-31
1.99E-34,38,205,LATE-ONSET RETINAL DEGENERATION (disorder),C565309,9,8.38E-31
1.34E-34,38,203,Hyperthyroxinemia,D006981,3,5.67E-31
1.34E-34,38,203,Tricuspid Atresia,D018785,3,5.67E-31
1.10E-34,38,202,"Lung Diseases, Fungal",D008172,2,4.66E-31
1.10E-34,38,202,Hypercapnia,D006935,2,4.66E-31
1.10E-34,38,202,Winchester syndrome (disorder),C536709,2,4.66E-31
1.10E-34,38,202,TORG-WINCHESTER SYNDROME,C536051,2,4.66E-31
1.99E-34,38,205,Multiple fibrofolliculomas,D058249,5,8.38E-31
9.04E-35,38,201,"Chromosome 8, monosomy 8p23 1",C537827,1,3.83E-31
9.04E-35,38,201,Tuberculoma,D014375,1,3.83E-31
9.04E-35,38,201,Intracranial Tuberculoma,D016862,1,3.83E-31
9.04E-35,38,201,"Menstruation, Retrograde",D008599,1,3.83E-31
9.04E-35,38,201,Noncommunicable Diseases,D000073296,1,3.83E-31
9.04E-35,38,201,Hemothorax,D006491,1,3.83E-31
9.04E-35,38,201,"Pancreatic Hypoplasia, Congenital, with Diabetes Mellitus and Congenital Heart Disease",C564011,1,3.83E-31
9.04E-35,38,201,Atrial Septal Defect 4,C566963,1,3.83E-31
9.04E-35,38,201,Atrial septal defect 2,C538263,1,3.83E-31
9.04E-35,38,201,Kasabach-Merritt syndrome,D059885,1,3.83E-31
9.04E-35,38,201,Xanthogranulomatous cholecystitis,C536762,1,3.83E-31
9.04E-35,38,201,"Factor 8 deficiency, acquired",C536392,1,3.83E-31
9.04E-35,38,201,"Atrial Fibrillation, Familial, 6",C567400,1,3.83E-31
9.04E-35,38,201,Yorifuji Okuno syndrome,C536714,1,3.83E-31
5.20E-34,38,210,Legg-Calve-Perthes Disease,D007873,17,2.19E-30
6.28E-34,38,211,Sudden Cardiac Arrest,D016757,18,2.64E-30
9.27E-34,39,230,"Foramen Ovale, Patent",D054092,32,3.90E-30
7.58E-34,38,212,"Amyloidosis, Familial",D028226,14,3.19E-30
2.54E-33,37,202,SMALL PATELLA SYNDROME,C535540,3,1.07E-29
3.72E-33,37,204,"Von Willebrand disease, platelet type",C536458,5,1.56E-29
3.07E-33,37,203,Barber Say syndrome,C537908,3,1.29E-29
2.54E-33,37,202,Prekallikrein deficiency,C562725,2,1.07E-29
2.09E-33,37,201,Idiopathic Multicentric Osteolyses,D010015,1,8.80E-30
2.09E-33,37,201,"Congenital thrombotic disease, due to Protein C deficiency",C535424,1,8.80E-30
2.09E-33,37,201,"Protein C Deficiency, Acquired",C567164,1,8.80E-30
2.09E-33,37,201,"CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 3",C567678,1,8.80E-30
2.09E-33,37,201,"THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE",C567353,1,8.80E-30
2.09E-33,37,201,Preeclampsia Eclampsia 4,C563724,1,8.80E-30
2.09E-33,37,201,"Thrombophilia, Hereditary, Due To Protein C Deficiency, Autosomal Dominant",C567163,1,8.80E-30
2.09E-33,37,201,Maxillary Diseases,D008439,1,8.80E-30
3.05E-32,88,1865,Obesity,D009765,1743,1.28E-28
1.14E-32,37,210,Sturge-Weber Syndrome,D013341,10,4.78E-29
6.75E-32,36,203,Heavy Chain Disease,D006362,4,2.83E-28
6.75E-32,36,203,Hemosiderosis,D006486,3,2.83E-28
1.17E-31,36,206,Hypesthesia,D006987,9,4.90E-28
5.61E-32,36,202,Ankle Injuries,D016512,2,2.35E-28
9.75E-32,36,205,Heart Neoplasm,D006338,5,4.09E-28
1.17E-31,36,206,"Aortic Aneurysm, Thoracoabdominal",D017545,6,4.90E-28
1.40E-31,36,207,Neurocutaneous Syndromes,D020752,8,5.87E-28
4.65E-32,36,201,"Atrioventricular Septal Defect, Partial, with Heterotaxy Syndrome",C565249,1,1.95E-28
1.40E-31,36,207,KUFOR-RAKEB SYNDROME,C537177,7,5.87E-28
2.01E-31,36,209,Trypanosomiasis,D014352,9,8.41E-28
4.37E-31,37,231,Pyruvate Carboxylase Deficiency Disease,D015324,36,1.83E-27
1.35E-30,37,238,Bicuspid aortic valve,C562388,47,5.65E-27
1.36E-30,36,220,Wolff-Parkinson-White Syndrome,D014927,21,5.66E-27
2.04E-30,35,205,Placenta Disorders,D010922,6,8.49E-27
2.04E-30,35,205,"Hyperthyroxinemia, Familial Dysalbuminemic",D050010,6,8.49E-27
1.19E-30,35,202,Spinal Cord Vascular Diseases,D020758,2,4.98E-27
4.71E-30,37,246,"Bone Diseases, Developmental",D001848,53,1.96E-26
9.95E-31,35,201,Hyperkeratotic Cutaneous Capillary-Venous Malformations Associated With Cerebral Capillary Malformations,C566153,1,4.16E-27
9.95E-31,35,201,Lipomatous neoplasm,D018205,1,4.16E-27
9.95E-31,35,201,Cavitary Optic Disc Anomalies,C566924,1,4.16E-27
9.95E-31,35,201,"SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, SKELETAL ABNORMALITIES",C566544,1,4.16E-27
9.95E-31,35,201,"Intracranial Hematoma, Traumatic",D020198,1,4.16E-27
9.95E-31,35,201,"CEREBELLAR ATAXIA, CAYMAN TYPE",C563363,1,4.16E-27
9.95E-31,35,201,Cavernous Malformations of CNS and Retina,C566152,1,4.16E-27
9.95E-31,35,201,"Hematoma, Subdural, Acute",D020199,1,4.16E-27
9.95E-31,35,201,Inflammatory Bowel Disease 19,C567372,1,4.16E-27
4.95E-29,35,224,Fuchs Endothelial Dystrophy,D005642,29,2.06E-25
2.89E-29,34,203,"CORTICAL DYSPLASIA OF TAYLOR, DYSPLASIA ONLY",C564583,3,1.21E-25
2.89E-29,34,203,"Focal Cortical Dysplasia of Taylor, Type IIb",C537067,3,1.21E-25
4.84E-29,34,206,Erythrokeratodermia variabilis,D056266,9,2.02E-25
5.74E-29,34,207,"Pachyonychia Congenita, Jadassohn Lewandowsky Type",D053549,8,2.39E-25
6.79E-29,34,208,Ichthyosis Bullosa of Siemens,D053560,9,2.82E-25
2.04E-29,34,201,Congenital Rubella Syndrome,D012410,1,8.52E-26
2.04E-29,34,201,"Night Blindness, Congenital Stationary, Autosomal Dominant 1",C566474,1,8.52E-26
2.04E-29,34,201,Retinitis Pigmentosa 4,C566706,1,8.52E-26
6.79E-29,34,208,Acantholysis,D000051,8,2.82E-25
8.03E-29,34,209,Symmetrical dyschromatosis of extremities,C535729,12,3.34E-25
1.83E-28,34,214,"Cafe au lait spots, multiple",C537421,17,7.62E-25
9.27E-28,33,206,Focal Dermal Hypoplasia,D005489,7,3.85E-24
4.03E-28,33,201,Arbovirus Infections,D001102,1,1.68E-24
4.03E-28,33,201,"Dehydrated Hereditary Stomatocytosis, Pseudohyperkalemia, and Perinatal Edema",C566369,1,1.68E-24
3.92E-27,33,215,Pathologic Neovascularization,D009389,16,1.63E-23
8.31E-27,34,239,Hemorrhagic Disorders,D006474,55,3.45E-23
6.47E-27,32,200,"Neuronal Intestinal Dysplasia, Type B",C537394,2,2.69E-23
1.05E-26,32,203,Renal tubular necrosis,D007673,3,4.37E-23
8.97E-27,32,202,"3-@METHYLGLUTACONIC ACIDURIA, TYPE I",C562801,2,3.72E-23
8.97E-27,32,202,Lattice corneal dystrophy Type II,C537459,2,3.72E-23
7.62E-27,32,201,Occipital Region Trauma,D006259,1,3.16E-23
2.57E-25,32,224,Atypical Hemolytic Uremic Syndrome,D065766,27,1.07E-21
3.00E-25,31,206,Extensively Drug-Resistant Tuberculosis,D054908,9,1.24E-21
1.89E-25,31,203,Congenital bronchogenic cyst,D001994,3,7.82E-22
1.38E-25,31,201,"Lymphedema, microcephaly and chorioretinopathy syndrome",C537711,1,5.73E-22
1.38E-25,31,201,Macrocephaly mesodermal hamartoma spectrum,C537716,1,5.73E-22
1.38E-25,31,201,Luteoma,D018311,1,5.73E-22
1.38E-25,31,201,Tension Pneumothorax,D011030,1,5.73E-22
1.38E-25,31,201,Suppurative Periapical Periodontitis,D010482,1,5.73E-22
1.38E-25,31,201,Familial multiple trichodiscomas,C536847,1,5.73E-22
1.38E-25,31,201,"Microcephaly with Chorioretinopathy, Autosomal Dominant",C563583,1,5.73E-22
1.37E-24,32,236,Geographic Atrophy,D057092,51,5.68E-21
7.10E-24,31,228,Fibrodysplasia Ossificans Progressiva,D009221,37,2.93E-20
4.36E-24,30,205,Velopharyngeal Insufficiency,D014681,7,1.80E-20
2.40E-24,30,201,Potocki-Lupski syndrome,C538355,2,9.92E-21
4.36E-24,30,205,Megaloblastic anemia due to inborn errors of metabolism,C538556,6,1.80E-20
3.76E-24,30,204,Intrinsic Factor Deficiency,C563242,4,1.55E-20
3.24E-24,30,203,Heparin cofactor II deficiency (disorder),C562865,3,1.34E-20
2.40E-24,30,201,Foodborne Disease,D005517,1,9.92E-21
2.40E-24,30,201,Scurvy,D012614,1,9.92E-21
2.40E-24,30,201,Teratogenesis,D064793,1,9.92E-21
1.39E-23,30,213,Mannose-Binding Protein Deficiency,C563602,14,5.72E-20
5.32E-23,29,203,"HIP DYSPLASIA, BEUKES TYPE",C564185,4,2.19E-19
6.13E-23,29,204,Glycogen Storage Disease Type IIb,D052120,5,2.53E-19
5.32E-23,29,203,Segmental glomerulosclerosis,C538457,3,2.19E-19
5.32E-23,29,203,"Mental Retardation, X-Linked 19",C563141,3,2.19E-19
7.07E-23,29,205,Preexcitation Syndrome,D011226,5,2.91E-19
4.60E-23,29,202,Emanuel syndrome,C535733,2,1.90E-19
3.98E-23,29,201,Abruzzo Erickson syndrome,C535559,1,1.64E-19
3.98E-23,29,201,Reginato Schiapachasse syndrome,C535519,1,1.64E-19
9.57E-22,28,204,"Spinal muscular atrophy, Jerash type",C535715,6,3.94E-18
7.26E-22,28,202,Platelet Glycoprotein IV Deficiency,C564245,3,2.99E-18
9.57E-22,28,204,"Keratoderma, Palmoplantar, Epidermolytic",D053546,4,3.94E-18
7.26E-22,28,202,chromosome 11q duplication syndrome,C538297,2,2.99E-18
6.32E-22,28,201,"Glanzmann Thrombasthenia, Autosomal Dominant",C566061,1,2.60E-18
2.53E-20,33,349,Craniofacial Abnormalities,D019465,177,1.04E-16
1.42E-20,27,204,Perisylvian syndrome,C536658,5,5.86E-17
1.85E-20,27,206,Communicable Diseases,D003141,9,7.60E-17
1.25E-20,27,203,"Epilepsy, Partial, with Variable Foci",C565785,3,5.13E-17
2.39E-20,27,208,TROPICAL CALCIFIC PANCREATITIS,C564276,9,9.84E-17
1.57E-19,26,202,Bohring syndrome,C537419,3,6.45E-16
1.78E-19,26,203,Steatocystoma multiplex,D062685,3,7.32E-16
2.42E-18,25,203,Glomerulopathy with fibronectin deposits,C536826,3,9.94E-15
1.90E-18,25,201,CHROMOSOME 9p DELETION SYNDROME,C538024,1,7.80E-15
1.90E-18,25,201,Marles Greenberg Persaud syndrome,C536022,1,7.80E-15
1.90E-18,25,201,FOCAL SEGMENTAL GLOMERULOSCLEROSIS 2,C565831,1,7.80E-15
1.90E-18,25,201,Anus Prolapse,D012005,1,7.80E-15
1.90E-18,25,201,"Bifid Nose, Autosomal Dominant",C535441,1,7.80E-15
2.85E-17,65,1758,Schizophrenia,D012559,1666,1.17E-13
2.48E-17,24,201,Familial antiphospholipid syndrome,C531622,1,1.02E-13
2.48E-17,24,201,"Bleeding Disorder, East Texas Type",C565275,1,1.02E-13
4.29E-16,23,204,Venous Insufficiency,D014689,6,1.76E-12
5.33E-16,23,206,Pancreatic Pseudocyst,D010192,6,2.18E-12
3.45E-16,23,202,THROMBOPHILIA DUE TO ACTIVATED PROTEIN C RESISTANCE (disorder),C566056,2,1.41E-12
3.09E-16,23,201,"Factor XIII, B Subunit, Deficiency Of",C567688,1,1.26E-12
3.97E-15,53,1340,Hypertensive disease,D006973,1190,1.63E-11
5.50E-15,22,205,Staphylococcal Scalded Skin Syndrome,D013206,7,2.25E-11
6.80E-14,34,611,Major Depressive Disorder,D003865,464,2.78E-10
4.47E-14,21,202,"Mental Retardation, Autosomal Dominant 4",C567240,4,1.83E-10
4.04E-14,21,201,"Ichthyosis with hypotrichosis, autosomal recessive",C536273,1,1.65E-10
4.04E-14,21,201,"Corneal Dystrophy, Congenital Stromal",C566452,1,1.65E-10
6.76E-13,20,206,Immune Complex Diseases,D007105,6,2.76E-09
4.67E-13,20,202,Epidermolysis Bullosa Simplex with Migratory Circinate Erythema,C563730,2,1.91E-09
3.82E-12,20,226,Oculocerebrorenal Syndrome,D009800,33,1.56E-08
4.14E-12,20,227,"Sterility, Postpartum",D007247,27,1.69E-08
4.22E-12,19,201,"Epilepsy, Familial Mesial Temporal Lobe",C566903,1,1.72E-08
2.25E-11,19,221,exudative macular degeneration,D057135,36,9.19E-08
8.77E-11,19,239,Angina Pectoris,D000787,53,3.57E-07
5.46E-11,18,205,Chromosome 2q37 deletion syndrome,C538317,6,2.22E-07
5.92E-11,18,206,Gyrate Atrophy,D015799,7,2.41E-07
3.62E-11,18,200,Facioscapulohumeral muscular dystrophy 1a,C536391,2,1.48E-07
4.64E-11,18,203,"Pancreatitis, Calcific",C566837,3,1.89E-07
4.64E-11,18,203,"WAARDENBURG SYNDROME, TYPE IIE",C536463,3,1.89E-07
4.27E-11,18,202,Left Bundle-Branch Block,D002037,2,1.74E-07
4.27E-11,18,202,Mitochondrial cytopathy,C540770,2,1.74E-07
3.93E-11,18,201,"Mitochondrial DNA Depletion Syndrome, Myopathic Form",C563698,1,1.60E-07
3.93E-11,18,201,Inflammatory Bowel Disease 10,C567021,1,1.60E-07
3.93E-11,18,201,"Glycogen Storage Disease of Heart, Lethal Congenital",C564888,1,1.60E-07
3.93E-11,18,201,Fasciculoventricular Accessory Pathway,D058606,1,1.60E-07
3.93E-11,18,201,"Polyhydramnios, Megalencephaly, And Symptomatic Epilepsy",C567020,1,1.60E-07
3.93E-11,18,201,"Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia",C564509,1,1.60E-07
3.93E-11,18,201,AICARDI-GOUTIERES SYNDROME 5 (disorder),C535608,1,1.60E-07
3.93E-11,18,201,AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency,C563876,1,1.60E-07
3.93E-11,18,201,"Carbohydrate Metabolism, Inborn Errors",D002239,1,1.60E-07
3.93E-11,18,201,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 6 (disorder)",C563436,1,1.60E-07
9.66E-10,28,605,Pain,D010146,447,3.92E-06
8.27E-10,18,242,Sleep Disorders,D012893,44,3.36E-06
4.01E-10,17,203,Hyperproinsulinemia,C562776,3,1.63E-06
7.86E-10,17,212,Vacuolar myopathy,C536522,13,3.19E-06
3.71E-10,17,202,Yunis Varon syndrome,C536719,2,1.51E-06
3.44E-10,17,201,Perioral Dermatitis,D019557,1,1.40E-06
3.44E-10,17,201,Naegeli syndrome,C538331,1,1.40E-06
4.60E-09,17,238,ATRICHIA WITH PAPULAR LESIONS,C565924,40,1.86E-05
3.48E-09,16,204,"EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE (disorder)",C563408,4,1.41E-05
3.48E-09,16,204,Sphingolipidoses,D013106,4,1.41E-05
3.02E-09,16,202,"CHARCOT-MARIE-TOOTH DISEASE, TYPE 4J",C566984,3,1.22E-05
5.66E-09,16,211,Benign symmetrical lipomatosis,C537837,11,2.29E-05
1.45E-08,17,257,Cholecystolithiasis,D041761,70,5.88E-05
2.81E-09,16,201,Carboxypeptidase N Deficiency,C562876,1,1.14E-05
2.81E-09,16,201,"Polymicrogyria, Bilateral Occipital",C567201,1,1.14E-05
2.81E-09,16,201,AMYOTROPHIC LATERAL SCLEROSIS 11,C567244,1,1.14E-05
3.07E-08,24,535,Myopathy,D009135,357,0.000124207
7.51E-08,21,437,Essential Hypertension,D000075222,255,0.000304028
2.25E-07,19,386,Ventricular Septal Defects,D006345,212,0.000908664
2.34E-07,15,241,Basal Cell Nevus Syndrome,D001478,43,0.000945517
4.86E-07,19,406,Hydrocephalus,D006849,236,0.00196529
1.51E-07,14,201,"Kallikrein, Decreased Urinary Activity of",C563653,1,0.000612341
1.51E-07,14,201,Subcorneal pustular dermatosis,D012872,1,0.000612341
1.79E-06,19,443,Fanconi Anemia,D005199,262,0.007228687
1.24E-06,14,239,Hyperlipoproteinemias,D006951,40,0.004986509
3.60E-06,20,509,Orbital separation excessive,D006972,351,0.014506997
3.82E-06,20,511,Anxiety Disorders,D001008,350,0.01538296
3.18E-06,14,259,"Fractures, Multiple",D000069076,71,0.01282551
1.11E-06,13,203,"Inclusion Body Myopathy, Autosomal Recessive",C538329,3,0.004472718
4.71E-06,16,346,Liver Failure,D017093,164,0.01896174
1.05E-06,13,202,Missed abortion,D000030,2,0.00423156
3.32E-06,13,224,Gall Bladder Diseases,D005705,25,0.013377538
9.91E-07,13,201,Maximal Voluntary Ventilation,D008451,1,0.004003041
9.91E-07,13,201,Sebaceous Gland Diseases,D012625,1,0.004003041
1.19E-05,13,252,DiGeorge Syndrome,D004062,59,0.047778531
2.13E-05,19,527,"Alcoholic Intoxication, Chronic",D000437,381,0.085590266
7.30E-06,12,205,ACTIVATED PI3K-DELTA SYNDROME,C585640,5,0.029332895
1.24E-05,12,216,Kashin-Beck Disease,D057767,19,0.049759477
6.95E-06,12,204,Insulin-Like Growth Factor I Deficiency,C563867,4,0.027913708
6.28E-06,12,202,Anisometropia,D015858,3,0.0252674
2.69E-05,19,536,Micrognathism,D008844,374,0.107961762
6.61E-06,12,203,"DIABETES MELLITUS, INSULIN-DEPENDENT, 2",C565100,3,0.026555094
1.95E-05,12,226,Thyroid Hormone Resistance Syndrome,D018382,31,0.078202381
3.38E-05,19,545,Cryptorchidism,D003456,382,0.13525784
6.28E-06,12,202,LETHAL CONGENITAL CONTRACTURE SYNDROME 1,C537194,2,0.0252674
6.28E-06,12,202,Myotubular Myopathy with Abnormal Genital Development,C564561,2,0.0252674
2.04E-05,12,227,Lipid Metabolism Disorders,D052439,28,0.081686669
3.22E-05,13,277,Hypotension,D007022,83,0.129175674
5.97E-06,12,201,"MACROPHTHALMIA, COLOBOMATOUS, WITH MICROCORNEA",C566533,1,0.02405855
5.97E-06,12,201,DNA Virus Infections,D004266,1,0.02405855
5.97E-06,12,201,Sexual Infantilism,D050035,1,0.02405855
5.97E-06,12,201,Froehlich's Syndrome,D007027,1,0.02405855
5.97E-06,12,201,Lethal Arthrogryposis With Anterior Horn Cell Disease,C567502,1,0.02405855
5.97E-06,12,201,Leukonychia totalis,C535889,1,0.02405855
5.97E-06,12,201,NEPHRONOPHTHISIS 4,C564640,1,0.02405855
7.30E-05,13,300,Erectile dysfunction,D007172,109,0.291949773
3.78E-05,11,204,"Leprosy, Multibacillary",D056006,7,0.151089657
3.45E-05,11,202,VACTERL Association With Hydrocephalus,C564751,4,0.138116775
6.08E-05,11,215,Hyperkeratosis lenticularis perstans,C538377,15,0.243437926
7.79E-05,11,221,Neurobehavioral Manifestations,D019954,32,0.311610434
0.000144372,2,2,Arthrogryposis,D001176,287,0.576911584
3.61E-05,11,203,Native American myopathy,C538343,3,0.144477916
8.79E-05,11,224,"CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT",C565145,26,0.351423184
0.000144372,2,2,Congenital clubfoot,D003025,182,0.576911584
0.000144372,2,2,Dyspnea,D004417,176,0.576911584
0.000144372,2,2,Kyphosis deformity of spine,D007738,155,0.576911584
3.30E-05,11,201,Vater Association With Macrocephaly And Ventriculomegaly,C564752,2,0.132130146
0.000144372,2,2,Muscle Hypertonia,D009122,109,0.576911584
0.000144372,2,2,Facial Paresis,D005158,85,0.576911584
0.000144372,2,2,Bell Palsy,D020330,84,0.576911584
0.000120009,11,232,Growth Hormone-Secreting Pituitary Adenoma,D049912,39,0.479677861
0.000144372,2,2,Pallor,D010167,55,0.576911584
0.000144372,2,2,Malignant hyperpyrexia due to anesthesia,D008305,43,0.576911584
0.000144372,2,2,Severe combined immunodeficiency due to adenosine deaminase deficiency,C531816,21,0.576911584
0.000186669,11,244,Hypotrichosis,D007039,53,0.741636892
3.30E-05,11,201,Cerebellar Granule Cell Hypertrophy and Megalencephaly,C563565,1,0.132130146
3.30E-05,11,201,CEREBELLOPARENCHYMAL DISORDER VI,C563564,1,0.132130146
3.30E-05,11,201,"Alopecia, Neurologic Defects, and Endocrinopathy Syndrome",C567425,1,0.132130146
0.000144372,2,2,Achromatopsia 1,C536021,13,0.576911584
0.000238428,11,251,Eating Disorders,D001068,66,0.94560664
0.000144372,2,2,"Hidradenitis suppurativa, familial",C538118,10,0.576911584
0.000245274,10,211,Parakeratosis,D010241,17,0.972510144
0.000218565,10,208,Prenatal Injuries,D049188,11,0.867265379
0.000218565,10,208,Recurrent respiratory papillomatosis,C535297,8,0.867265379
0.000194343,10,205,Bronchiolitis Obliterans Organizing Pneumonia,D018549,6,0.771734533
0.000194343,10,205,Lymph Node Tuberculosis,D014388,6,0.771734533
0.000202152,10,206,Histoplasmosis,D006660,6,0.80234216
0.000394807,10,224,Growth Disorders,D006130,36,1
0.000179483,10,203,Craniofrontonasal dysplasia,C536456,4,0.713443823
0.00050178,11,274,Neuralgia,D009437,86,1
0.000186788,10,204,CAPILLARY MALFORMATION-ARTERIOVENOUS MALFORMATION (disorder),C564254,4,0.74192333
0.000165591,10,201,Mastodynia,D059373,3,0.659715408
0.000438396,10,227,Dislocations,D004204,37,1
0.000172419,10,202,Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia,C565328,3,0.685711002
0.000179483,10,203,Teratoma of testis,C562472,3,0.713443823
0.000172419,10,202,Forebrain Defects,C566067,2,0.685711002
0.000779992,11,289,Anorexia,D000855,101,1
0.000613628,10,237,"Muscular Dystrophy, Oculopharyngeal",D039141,37,1
0.000698295,10,241,Sleep Apnea Syndromes,D012891,51,1
0.000165591,10,201,"Renal Hypodysplasia, Nonsyndromic, 1",C563661,1,0.659715408
0.000165591,10,201,Hantavirus Pulmonary Syndrome,D018804,1,0.659715408
0.000165591,10,201,Vesicoureteral Reflux 2,C567053,1,0.659715408
0.000165591,10,201,"Tuberculosis, Bovine",D014380,1,0.659715408
0.000165591,10,201,Baraitser Brett Piesowicz syndrome,C537905,1,0.659715408
0.000165591,10,201,SPASTIC PARAPLEGIA 23 (disorder),C536859,1,0.659715408
0.001172968,10,258,Gilles de la Tourette syndrome,D005879,84,1
0.001172968,10,258,Situs Inversus,D012857,72,1
0.001522349,11,314,Cleft upper lip,D002971,154,1
0.001829028,16,581,Anxiety,D001007,424,1
0.001473628,10,266,Connective Tissue Diseases,D003240,77,1
0.00102499,9,210,INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE AND FRONTOTEMPORAL DEMENTIA,C563476,14,1
0.000835427,9,204,MYOTILINOPATHY,C563775,7,1
0.001208364,9,215,Glycogen Storage Disease Type I,D005953,18,1
0.000675448,9,198,Amniotic Bands,D000652,4,1
0.001248038,9,216,Xanthomatosis,D014973,17,1
0.000864864,9,205,Lichen planus follicularis,C535892,6,1
0.000806811,9,203,X-linked hypogammaglobulinemia,C562478,4,1
0.001758007,9,227,Gerstmann-Straussler-Scheinker Disease,D016098,31,1
0.000751972,9,201,Gianotti-Crosti Syndrome,D000169,3,1
0.000778998,9,202,Cowpox,D015605,3,1
0.003092202,11,344,Drug abuse,D019966,206,1
0.000806811,9,203,"NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE V",C563443,3,1
0.000778998,9,202,Prosthesis Loosening,D011475,2,1
0.000778998,9,202,Kaufman oculocerebrofacial syndrome,C537013,2,1
0.003361716,9,250,Drug Withdrawal Symptoms,D013375,52,1
0.006059981,15,599,Autism Spectrum Disorders,D000067877,501,1
0.004795792,9,264,Prader-Willi Syndrome,D011218,85,1
0.000751972,9,201,Osteopathia striata cranial sclerosis,C536053,1,1
0.000751972,9,201,Nakajo syndrome,C538334,1,1
0.000751972,9,201,Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma,C566600,1,1
0.000751972,9,201,"Methylmalonic Aciduria, CblD Type, Variant 2",C564743,1,1
0.000751972,9,201,"DIABETES MELLITUS, NONINSULIN-DEPENDENT, 2 (disorder)",C563323,1,1
0.000751972,9,201,Necrobiosis Lipoidica Diabeticorum,D009335,1,1
0.00709805,13,495,Hepatomegaly,D006529,346,1
0.004594928,8,215,"Hypotension, Orthostatic",D007024,24,1
0.004224886,8,212,"Depression, Postpartum",D019052,15,1
0.003991265,8,210,Triglyceride storage disease with ichthyosis,C536560,12,1
0.004106793,8,211,Lower Urinary Tract Symptoms,D059411,12,1
0.004468916,8,214,"Nuchal bleb, familial",C537852,14,1
0.007548758,8,234,Dizziness,D004244,49,1
0.011376093,12,468,Mood Disorders,D019964,299,1
0.008320426,8,238,Vertigo,D014717,50,1
0.008320426,8,238,Endocardial Cushion Defects,D004694,47,1
0.003154944,8,202,Gillespie syndrome,C536370,3,1
0.003251278,8,203,Ulnar-mammary syndrome,C536937,3,1
0.003154944,8,202,PARKINSON DISEASE 12,C564486,2,1
0.003154944,8,202,"Myelitis, Transverse",D009188,2,1
0.003154944,8,202,Deciduoma,D033301,2,1
0.014252067,8,262,MAJOR AFFECTIVE DISORDER 2,C564108,88,1
0.017339001,10,381,Osteogenesis Imperfecta,D010013,198,1
0.016123459,8,268,Ichthyoses,D007057,83,1
0.01781388,8,273,Anorexia Nervosa,D000856,86,1
0.02084037,9,336,Respiratory Insufficiency,D012131,164,1
0.023946208,1,2,Finding of Mean Corpuscular Hemoglobin,D004909,315,1
0.024091541,10,402,Myopia,D009216,244,1
0.003060847,8,201,Pseudodementia,D005162,1,1
0.003060847,8,201,Huntington Disease-Like Syndrome,C580174,1,1
0.028556024,12,534,Curvature of spine,D013121,379,1
0.023946208,1,2,Icterus,D007565,141,1
0.027502053,10,411,Deafness,D003638,257,1
0.014820076,7,213,"Disruptive, Impulse Control, and Conduct Disorders",D007174,18,1
0.016629327,7,218,Pathological fracture,D005598,25,1
0.027516157,9,353,Hypospadias,D007021,177,1
0.012840034,7,207,Central Precocious Puberty,C562787,10,1
0.015887812,7,216,Hypernatremia,D006955,18,1
0.017395047,7,220,Hypobetalipoproteinemias,D006995,22,1
0.013804601,7,210,Violence,D014754,11,1
0.011630757,7,203,Bruxism,D002012,7,1
0.017395047,7,220,Adult Rickets,D010018,21,1
0.017787102,7,221,Tangier Disease,D013631,22,1
0.011925001,7,204,"NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE",C536404,7,1
0.019417726,7,225,"Lymphangioma, Cystic",D018191,28,1
0.033019166,10,424,hearing impairment,D034381,274,1
0.023946208,1,2,Hyperpigmentation,D017495,49,1
0.021599836,7,230,"Truncus Arteriosus, Persistent",D014339,33,1
0.022518568,7,232,Malabsorption Syndrome,D008286,38,1
0.029192756,8,300,Nicotine Dependence,D014029,113,1
0.012840034,7,207,"DIARRHEA 5, WITH TUFTING ENTEROPATHY, CONGENITAL",C567703,7,1
0.011630757,7,203,"FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED",C579991,5,1
0.023946904,7,235,Hypokalemia,D007008,37,1
0.011925001,7,204,Somatostatinoma,D013005,5,1
0.026464174,7,240,Muscular fasciculation,D005207,47,1
0.029156585,7,245,Amphetamine-Related Disorders,D019969,69,1
0.028058301,7,243,Tardive Dyskinesia,D000071057,47,1
0.011925001,7,204,Kwashiorkor,D007732,4,1
0.011925001,7,204,"Acidosis, Respiratory",D000142,4,1
0.011925001,7,204,Deficiency of pyruvate kinase,C564858,4,1
0.035704476,1,3,"Mental Retardation, X-Linked",D038901,98,1
0.023946208,1,2,PITUITARY DWARFISM I,C537404,19,1
0.023946208,1,2,Vitamin A Deficiency,D014802,18,1
0.011341809,7,202,Empty Sella Syndrome,D004652,3,1
0.011341809,7,202,"MENTAL RETARDATION, X-LINKED 78",C564489,3,1
0.011341809,7,202,"MENTAL RETARDATION, X-LINKED 91 (disorder)",C564482,3,1
0.011341809,7,202,"POPLITEAL PTERYGIUM SYNDROME, LETHAL TYPE",C564874,3,1
0.011630757,7,203,"MENTAL RETARDATION, X-LINKED 52",C564502,3,1
0.011630757,7,203,"Mental Retardation, X-Linked, Znf711-Related",C567583,3,1
0.03635982,7,257,Congenital pectus carinatum,D066166,75,1
0.037008613,7,258,Klinefelter Syndrome,D007713,73,1
0.03635982,7,257,"Anemia, Diamond-Blackfan",D029503,63,1
0.037008613,7,258,Idiopathic hypogonadotropic hypogonadism,C562785,61,1
0.023946208,1,2,Kearns-Sayre syndrome,D007625,10,1
0.011341809,7,202,"MENTAL RETARDATION, X-LINKED 77",C564511,2,1
0.011341809,7,202,"MENTAL RETARDATION, X-LINKED 23",C563144,2,1
0.011341809,7,202,"MENTAL RETARDATION, X-LINKED 42",C564524,2,1
0.011341809,7,202,"MENTAL RETARDATION, X-LINKED 53",C564533,2,1
0.011341809,7,202,"MENTAL RETARDATION, X-LINKED 89",C564036,2,1
0.011341809,7,202,"MENTAL RETARDATION, X-LINKED 14",C537454,2,1
0.011341809,7,202,"Mental Retardation, X-Linked 92",C564483,2,1
0.011341809,7,202,"MENTAL RETARDATION, X-LINKED 81",C564515,2,1
0.011341809,7,202,Mesomelia-synostoses syndrome,C537348,2,1
0.011341809,7,202,"MENTAL RETARDATION, X-LINKED 2 (disorder)",C563135,2,1
0.011341809,7,202,Primary cortisol resistance,C535280,2,1
0.011341809,7,202,"MENTAL RETARDATION, X-LINKED 95",C567470,2,1
0.011341809,7,202,"MENTAL RETARDATION, X-LINKED 73",C564528,2,1
0.011341809,7,202,"Gaze Palsy, Familial Horizontal, with Progressive Scoliosis",C564593,2,1
0.011341809,7,202,"MENTAL RETARDATION, X-LINKED 20",C563142,2,1
0.011341809,7,202,"MENTAL RETARDATION, X-LINKED 50",C564713,2,1
0.011341809,7,202,Trichotillomania,D014256,2,1
0.011341809,7,202,"MENTAL RETARDATION, X-LINKED 82",C564496,2,1
0.011341809,7,202,"MENTAL RETARDATION, X-LINKED 84",C564501,2,1
0.05550794,8,342,Narcolepsy,D009290,208,1
0.043561691,6,212,Exfoliation Syndrome,D017889,19,1
0.049602558,6,219,Fetal Death,D005313,26,1
0.044394781,6,213,Hemiplegia,D006429,17,1
0.042738506,6,211,Malignant Carcinoid Syndrome,D008303,15,1
0.058092878,6,228,RENAL ADYSPLASIA,C563261,41,1
0.041121758,6,209,Dysferlinopathy,C537995,13,1
0.054218359,6,224,Lipoidosis,D008064,31,1
0.044394781,6,213,"Hyperkeratosis, Epidermolytic",D017488,16,1
0.043561691,6,212,Hyperlipoproteinemia Type I,D008072,15,1
0.011058106,7,201,Neurogenic arthropathy,D001177,1,1
0.011058106,7,201,Erysipelothrix infection,D004889,1,1
0.011058106,7,201,Left Ventricular Function,D016277,1,1
0.011058106,7,201,"Deafness, Cochlear, with Myopia and Intellectual Impairment",C565645,1,1
0.011058106,7,201,Leukocyte Disorders,D007960,1,1
0.047826645,6,217,Hypoalphalipoproteinemias,D052456,19,1
0.043561691,6,212,X-linked hydrocephalus syndrome,C536078,14,1
0.042738506,6,211,Junctional Epidermolysis Bullosa,D016109,13,1
0.055171801,6,225,Ectropion,D004483,29,1
0.063164239,6,233,Endocrine System Diseases,D004700,48,1
0.041925204,6,210,"Hypothermia, Accidental",D007035,12,1
0.044394781,6,213,"Dyskinesia, Medication-Induced",D004409,14,1
0.043561691,6,212,Familial hypobetalipoproteinemia,C566267,13,1
0.046953712,6,216,Hyperlipoproteinemia Type III,D006952,16,1
0.059086846,6,229,Nail abnormality,D009264,34,1
0.04609077,6,215,Female Urogenital Diseases,D052776,15,1
0.0452378,6,214,Thymus Hyperplasia,D013952,14,1
0.064208981,6,234,Opiate Addiction,D009293,45,1
0.063164239,6,233,Chronic pain,D059350,42,1
0.061105231,6,231,Pituitary dwarfism,D004393,36,1
0.023946208,1,2,Eosinophilic myositis (disorder),C535895,3,1
0.066328943,6,236,Restless Legs Syndrome,D012148,45,1
0.066328943,6,236,Hemoglobinopathies,D006453,40,1
0.066328943,6,236,Tooth Abnormalities,D014071,39,1
0.038006,6,205,Subcortical Band Heterotopia,D054221,7,1
0.040328143,6,208,Adult-onset citrullinemia type 2,C538053,8,1
0.038770293,6,206,Patchy alopecia,C531609,7,1
0.078713738,6,247,Knee joint valgus deformity,D056304,66,1
0.078713738,6,247,Heroin Dependence,D006556,59,1
0.038006,6,205,Opsoclonus-Myoclonus Syndrome,D053578,6,1
0.036506528,6,203,As If Personality,D010554,5,1
0.079900243,6,248,"Hyperparathyroidism, Primary",D049950,49,1
0.087229766,6,254,Cushing Syndrome,D003480,63,1
0.038006,6,205,Circadian Rhythm Disorders,D021081,5,1
0.038006,6,205,Epiglottitis,D004826,5,1
0.038006,6,205,Multiple pterygium syndrome,C537377,5,1
0.096232828,6,261,"Hip Dislocation, Congenital",D006618,81,1
0.036506528,6,203,"Leukoplakia, Hairy",D017733,4,1
0.037251423,6,204,ENDPLATE ACETYLCHOLINESTERASE DEFICIENCY (disorder),C566415,4,1
0.037251423,6,204,Glut1 Deficiency Syndrome,C536830,4,1
0.037251423,6,204,Anti-N-Methyl-D-Aspartate Receptor Encephalitis,D060426,4,1
0.105714637,6,268,"Muscular Dystrophies, Limb-Girdle",D049288,84,1
0.109922302,6,271,Oligospermia,D009845,95,1
0.035771283,6,202,"Basal ganglia disease, biotin-responsive",C537658,3,1
0.035771283,6,202,17-Hydroxysteroid Dehydrogenase Deficiency,C537805,3,1
0.035771283,6,202,Prinzmetal's variant angina,C536421,3,1
0.035771283,6,202,Obsessive-Compulsive Personality,D003193,3,1
0.035771283,6,202,Lyme Neuroborreliosis,D020852,3,1
0.036506528,6,203,Spina Bifida Cystica,D016137,3,1
0.036506528,6,203,Carnitine-Acylcarnitine Translocase Deficiency,C562812,3,1
0.036506528,6,203,Intracranial Hypotension,D019585,3,1
0.12305173,6,280,Class III malocclusion,D008313,104,1
0.070140289,1,6,Mixed Connective Tissue Disease,D008947,13,1
0.148189616,6,296,Platelet Count measurement,D010976,162,1
0.032926117,6,198,"Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked",C564467,2,1
0.118617697,5,215,Astigmatism,D001251,43,1
0.035771283,6,202,Haemophilus influenzae Meningitis Type B,D008583,2,1
0.035771283,6,202,"ICHTHYOSIS, LEUKOCYTE VACUOLES, ALOPECIA, AND SCLEROSING CHOLANGITIS",C564365,2,1
0.158176173,6,302,Hypogonadotropic hypogonadism,D007006,116,1
0.047321794,1,4,Balo's Concentric Sclerosis,D002549,3,1
0.130742994,5,222,Gingival Overgrowth,D019214,43,1
0.122025548,5,217,Esotropia,D004948,33,1
0.105452892,5,207,Ophthalmoparesis,D009886,18,1
0.139735276,5,227,Refractive Errors,D012030,44,1
0.186175408,6,318,Contracture,D003286,151,1
0.12374658,5,218,Ectopia Lentis,D004479,26,1
0.11194087,5,211,Mucopolysaccharidosis IV,D009085,18,1
0.130742994,5,222,Antisocial Personality Disorder,D000987,30,1
0.156580969,5,236,Hip Dislocation,D006617,60,1
0.127222483,5,220,Hallux Valgus,D006215,27,1
0.141565823,5,228,Ptosis,D011391,39,1
0.141565823,5,228,Amelogenesis Imperfecta,D000567,39,1
0.125478917,5,219,Spasmodic torticollis,D014103,25,1
0.137915315,5,226,Hip joint varus deformity - observation,D060905,34,1
0.120315896,5,216,Retinal Dysplasia,D015792,21,1
0.120315896,5,216,Etat Marbre,D009069,21,1
0.116931024,5,214,Stillbirth,D050497,19,1
0.168256139,5,242,Waist Circumference,D055105,73,1
0.158502883,5,237,MAJOR AFFECTIVE DISORDER 7,C567529,56,1
0.136106024,5,225,Absence of septum pellucidum,C535562,31,1
0.158502883,5,237,MAJOR AFFECTIVE DISORDER 8,C567530,55,1
0.158502883,5,237,MAJOR AFFECTIVE DISORDER 9,C567531,55,1
0.150874359,5,233,Dental Enamel Hypoplasia,D003744,45,1
0.152766617,5,234,NEUROTICISM,D000075384,47,1
0.122025548,5,217,Pena-Shokeir syndrome type I,C536647,21,1
0.125478917,5,219,Astrocytosis,D005911,23,1
0.141565823,5,228,Genu varum,D056305,35,1
0.10705695,5,208,"Carney Complex, Type 1",D056733,14,1
0.128977201,5,221,ANONYCHIA,C536377,25,1
0.176225512,5,246,Forced expiratory volume function,D005541,83,1
0.137915315,5,226,Anhedonia,D059445,31,1
0.137915315,5,226,Epidermolysis Bullosa,D004820,31,1
0.105452892,5,207,Sensory hearing loss,D006319,13,1
0.125478917,5,219,Dentinogenesis Imperfecta,D003811,22,1
0.156580969,5,236,Hoarseness,D006685,49,1
0.148992168,5,232,Bulimia Nervosa,D052018,40,1
0.152766617,5,234,Mitral Valve Insufficiency,D008944,44,1
0.118617697,5,215,Choroid Plexus Papilloma,D020288,18,1
0.118617697,5,215,Cholesteryl Ester Transfer Protein Deficiency,C564591,18,1
0.100713345,5,204,Breech Presentation,D001946,11,1
0.10705695,5,208,Hyperacusis,D012001,13,1
0.143406872,5,229,Polyuria,D011141,33,1
0.115255949,5,213,Scleroatonic muscular dystrophy,C537521,16,1
0.139735276,5,227,Childhood Ataxia with Central Nervous System Hypomyelinization,D056784,30,1
0.120315896,5,216,Alcohol Withdrawal Delirium,D000430,18,1
0.105452892,5,207,Poikiloderma of Kindler,C536321,12,1
0.128977201,5,221,Diabetes Insipidus,D003919,22,1
0.116931024,5,214,Endomyocardial Fibrosis,D004719,16,1
0.11194087,5,211,Neurogenic Inflammation,D020078,14,1
0.115255949,5,213,Metatarsal Valgus,D000070591,15,1
0.120315896,5,216,"Psychoses, Substance-Induced",D011605,17,1
0.130742994,5,222,Hyperprolactinemia,D006966,22,1
0.10705695,5,208,Lenticulostriate Disorders,D001480,12,1
0.110301004,5,210,Platybasia,D010985,13,1
0.110301004,5,210,ARTERIAL TORTUOSITY SYNDROME,C565942,13,1
0.118617697,5,215,Adrenocorticotropic hormone (ACTH) deficiency (disorder),C535668,16,1
0.118617697,5,215,Zollinger-Ellison syndrome,D015043,16,1
0.125478917,5,219,Pseudoachondroplasia,C535819,19,1
0.176225512,5,246,MAJOR AFFECTIVE DISORDER 4,C567073,66,1
0.176225512,5,246,MAJOR AFFECTIVE DISORDER 6,C567075,66,1
0.087161799,5,195,"Thrombotic thrombocytopenic purpura, acquired",C536901,7,1
0.178240218,5,247,MAJOR AFFECTIVE DISORDER 1,C565111,68,1
0.116931024,5,214,Acrodysostosis,C538179,15,1
0.116931024,5,214,"Cutis Laxa, Autosomal Recessive, Type I",C562628,15,1
0.11194087,5,211,Allergy to peanuts,D021183,13,1
0.105452892,5,207,Paraparesis,D020335,11,1
0.120315896,5,216,Muscle eye brain disease,D058494,16,1
0.115255949,5,213,Agoraphobia,D000379,14,1
0.10705695,5,208,Bladder Diverticulum,C562406,11,1
0.10705695,5,208,Glossoptosis,D065710,11,1
0.174219654,5,245,"Anus, Imperforate",D001006,56,1
0.170234871,5,243,Holoprosencephaly,D016142,50,1
0.103860898,5,206,Gigantism,D005877,10,1
0.103860898,5,206,Congenital torticollis,C535425,10,1
0.11194087,5,211,Supravalvular aortic stenosis,D021921,12,1
0.100713345,5,204,Retinoschisis,D041441,9,1
0.105452892,5,207,Miyoshi myopathy,C537480,10,1
0.174219654,5,245,Hyperbilirubinemia,D006932,51,1
0.113592541,5,212,Bethlem myopathy,C535436,12,1
0.113592541,5,212,Osteogenesis imperfecta type IV (disorder),C536045,12,1
0.110301004,5,210,Frontotemporal Dementia With Motor Neuron Disease,C566288,11,1
0.172222741,5,244,"Myasthenic Syndromes, Congenital",D020294,47,1
0.190508749,5,253,Lordosis,D008141,71,1
0.10705695,5,208,"Hernia, Femoral",D006550,10,1
0.10705695,5,208,Corneal Scar,D065306,10,1
0.231439291,6,342,Photophobia,D020795,176,1
0.11194087,5,211,Osteogenesis imperfecta type III (disorder),C536044,11,1
0.11194087,5,211,Cobblestone Lissencephaly,D054222,11,1
0.103860898,5,206,Autosomal Dominant Nocturnal Frontal Lobe Epilepsy,C579932,9,1
0.103860898,5,206,Polymorphous corneal dystrophy,C562745,9,1
0.180263674,5,248,Common Migraine,D020326,53,1
0.108673009,5,209,Analgesic Overuse Headache,D051271,10,1
0.184336444,5,250,Congenital aneurysm of ascending aorta,C562834,55,1
0.105452892,5,207,"Spondyloepiphyseal dysplasia, congenita",C535788,9,1
0.105452892,5,207,Visceral Pain,D059265,9,1
0.100713345,5,204,Laryngostenosis,D007829,8,1
0.100713345,5,204,Lipoblastoma,D062689,8,1
0.10705695,5,208,Cor pulmonale,D011660,9,1
0.205191405,5,260,Syndactyly,D013576,77,1
0.103860898,5,206,"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B",C535899,8,1
0.103860898,5,206,"SHORT STATURE, IDIOPATHIC, X-LINKED",C564479,8,1
0.105452892,5,207,"Osteogenesis imperfecta, dominant perinatal lethal",C536042,8,1
0.105452892,5,207,"RETINAL NONATTACHMENT, NONSYNDROMIC CONGENITAL",C565633,8,1
0.100713345,5,204,Peritonsillar Abscess,D000039,7,1
0.102281029,5,205,Cicatrization,D002921,7,1
0.102281029,5,205,Ureterocele,D014518,7,1
0.23118979,5,272,Neonatal Hypotonia,D009123,104,1
0.103860898,5,206,Alcohol Withdrawal Seizures,D020270,7,1
0.103860898,5,206,"Leukocyte Adhesion Deficiency, Type III",C567555,7,1
0.097614769,5,202,Alkaptonuria,D000474,6,1
0.035045655,6,201,Burnett Schwartz Berberian syndrome,C537412,1,1
0.035045655,6,201,Ramon Syndrome,C535285,1,1
0.035045655,6,201,"Amyotrophic Lateral Sclerosis, Chmp2B-Related",C563708,1,1
0.035045655,6,201,Manz syndrome,C535709,1,1
0.035045655,6,201,"Insulin Receptor, Defect in",C562709,1,1
0.035045655,6,201,"Leydig Cell Adenoma, Somatic, with Male-Limited Precocious Puberty",C567168,1,1
0.035045655,6,201,"Hypomagnesemia 4, Renal",C567127,1,1
0.035045655,6,201,Chancroids,D002602,1,1
0.035045655,6,201,Inflammatory Bowel Disease 14,C567383,1,1
0.035045655,6,201,Sebocystomatosis,C580471,1,1
0.035045655,6,201,"Leydig Cell Hypoplasia, Type II",C562567,1,1
0.035045655,6,201,"Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans",C562710,1,1
0.035045655,6,201,"Myopia, susceptibility to",C536105,1,1
0.035045655,6,201,Paragonimiasis,D010237,1,1
0.035045655,6,201,"Cerebellar Ataxia, Deafness, and Narcolepsy",C565825,1,1
0.035045655,6,201,Meier Blumberg Imahorn syndrome,C536148,1,1
0.035045655,6,201,"Hypomagnesemia 5, Renal, with Ocular Involvement",C565423,1,1
0.035045655,6,201,Ehlers-Danlos syndrome type 5,C536197,1,1
0.035045655,6,201,"Vascular Malformation, Primary Intraosseous",C564648,1,1
0.035045655,6,201,"Hyperinsulinemic Hypoglycemia, Familial, 5",C566494,1,1
0.105452892,5,207,Geleophysic dysplasia,C535662,7,1
0.105452892,5,207,Oral Dyskinesia,D020820,7,1
0.105452892,5,207,Transposition of Great Vessels,D014188,7,1
0.105452892,5,207,Pyloric Atresia,C562561,7,1
0.099157906,5,203,"Periventricular Heterotopia, X-Linked",D054091,6,1
0.099157906,5,203,"Corneal Dystrophy, Band-Shaped",C562399,6,1
0.100713345,5,204,Calvarial hyperostosis,C537963,6,1
0.100713345,5,204,Chandler syndrome,D057129,6,1
0.100713345,5,204,CORNEAL ENDOTHELIAL DYSTROPHY 2,C536439,6,1
0.100713345,5,204,Laryngismus,D007826,6,1
0.102281029,5,205,Pulmonary Valve Insufficiency,D011665,6,1
0.102281029,5,205,"Ehlers-Danlos Syndrome, Type IV",D004535,6,1
0.102281029,5,205,Skin Wrinkling,D015595,6,1
0.102281029,5,205,"Lipid Metabolism, Inborn Errors",D008052,6,1
0.102281029,5,205,Eichsfeld type congenital muscular dystrophy,C535683,6,1
0.102281029,5,205,Epidermolysis bullosa with pyloric atresia,C535377,6,1
0.408043106,31,2445,Intellectual Disability,D008607,2319,1
0.103860898,5,206,"DYSTONIA, DOPA-RESPONSIVE, WITH OR WITHOUT HYPERPHENYLALANINEMIA, AUTOSOMAL RECESSIVE (disorder)",C537537,6,1
0.103860898,5,206,Alpha-Sarcoglycanopathies,D058088,6,1
0.103860898,5,206,Epidermolysis bullosa inversa dystrophica,C535958,6,1
0.103860898,5,206,Neonatal Abstinence Syndrome,D009357,6,1
0.103860898,5,206,Ehlers-Danlos syndrome type 1,C536194,6,1
0.242295709,5,277,Cocaine-Related Disorders,D019970,88,1
0.251282911,5,281,Obsessive-Compulsive Disorder,D009771,99,1
0.099157906,5,203,Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy,C563990,5,1
0.099157906,5,203,Keratitis-Ichthyosis-Deafness Syndrome,C580224,5,1
0.100713345,5,204,Familial Tremor,D020329,5,1
0.100713345,5,204,"Corneal Dystrophy, Juvenile Epithelial of Meesmann",D053559,5,1
0.100713345,5,204,RIPPLING MUSCLE DISEASE 1,C535686,5,1
0.100713345,5,204,"MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY",C536090,5,1
0.100713345,5,204,Ectopia lentis isolated,C536184,5,1
0.100713345,5,204,Oculomotor Nerve Paralysis,D015840,5,1
0.102281029,5,205,"EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE",C567527,5,1
0.102281029,5,205,Severe autosomal recessive muscular dystrophy of childhood - North African type (disorder),C535900,5,1
0.102281029,5,205,"Collagenopathy, type 2 alpha 1",C535964,5,1
0.102281029,5,205,Adult junctional epidermolysis bullosa (disorder),C562639,5,1
0.102281029,5,205,Amelogenesis imperfecta local hypoplastic form,C538240,5,1
0.102281029,5,205,Tricuspid Valve Prolapse,D014263,5,1
0.093059722,5,199,Epithelial Recurrent Erosion Dystrophy,C565155,4,1
0.332298103,6,391,Body mass index,D015992,310,1
0.283353518,5,295,Hypodontia,D000848,112,1
0.097614769,5,202,"Epilepsy, Opercular",D017034,4,1
0.097614769,5,202,Larsen syndrome,C580241,4,1
0.097614769,5,202,"Memory, Short-Term",D008570,4,1
0.097614769,5,202,Congenital absence of parathyroid gland,C563238,4,1
0.292664702,5,299,Delayed Puberty,D011628,120,1
0.099157906,5,203,Lipoid Proteinosis of Urbach and Wiethe,D008065,4,1
0.099157906,5,203,"Chylothorax, congenital",C535461,4,1
0.099157906,5,203,Scheuermann's Disease,D012544,4,1
0.099157906,5,203,Organothiophosphonate Poisoning,D062025,4,1
0.099157906,5,203,Psychomotor Performance,D011597,4,1
0.099157906,5,203,Fibromuscular Dysplasia,C537929,4,1
0.099157906,5,203,"Amelogenesis Imperfecta, Type III",C562880,4,1
0.099157906,5,203,Microspherophakia,C563255,4,1
0.099157906,5,203,"Dentin dysplasia, type 1",C538215,4,1
0.100713345,5,204,Bedwetting,D053206,4,1
0.100713345,5,204,"Myasthenic Syndrome, Congenital, with Facial Dysmorphism, associated with Acetylcholine Receptor Deficiency",C563829,4,1
0.100713345,5,204,"Fingerprints, Absence of",C565010,4,1
0.100713345,5,204,"Hypothyroidism, Congenital, Nongoitrous, 4",C000603735,4,1
0.100713345,5,204,Retinal Hemorrhage,D012166,4,1
0.100713345,5,204,Subungual exostoses,C535723,4,1
0.100713345,5,204,Ehlers-Danlos syndrome type 2,C536195,4,1
0.100713345,5,204,"Isolated Growth Hormone Deficiency, Type II",C562704,4,1
0.100713345,5,204,"Corneal Dystrophy, Subepithelial Mucinous",C567547,4,1
0.363814847,7,483,Muscle Weakness,D018908,310,1
0.090085526,5,197,"Deafness, Autosomal Dominant 13",C566612,3,1
0.344662027,5,321,"Breast Cancer, Familial",C562840,133,1
0.097614769,5,202,Pulmonary Arterial Remodeling,D066253,3,1
0.097614769,5,202,Thoracic Diseases,D013896,3,1
0.097614769,5,202,Kniest dysplasia,C537207,3,1
0.097614769,5,202,Melorheostosis,D008557,3,1
0.097614769,5,202,"Hyperinsulinemic hypoglycemia, familial, 6",C538375,3,1
0.097614769,5,202,Neuromuscular Junction Diseases,D020511,3,1
0.097614769,5,202,Fibrochondrogenesis,C562524,3,1
0.099157906,5,203,"Myasthenic Syndrome, Congenital, Fast-Channel",C563832,3,1
0.099157906,5,203,Self-Healing Collodion Baby,C565473,3,1
0.099157906,5,203,Uncombable hair syndrome,C536939,3,1
0.099157906,5,203,Weil Disease,D014895,3,1
0.099157906,5,203,Harlequin type ichthyosis,C538424,3,1
0.099157906,5,203,Vascular calcification,D061205,3,1
0.099157906,5,203,"Cutis laxa, recessive",C536225,3,1
0.099157906,5,203,BASAL LAMINAR DRUSEN (disorder),C563034,3,1
0.099157906,5,203,"Cutis Laxa, Autosomal Dominant",C562627,3,1
0.099157906,5,203,Achondrogenesis,C579878,3,1
0.099157906,5,203,"Parkinson Disease 6, Autosomal Recessive Early-Onset",C565276,3,1
0.099157906,5,203,Pulmonary Atresia with Intact Ventricular Septum,C562832,3,1
0.099157906,5,203,Hyaloideoretinal degeneration of Wagner,C536075,3,1
0.099157906,5,203,"EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE",C562625,3,1
0.099157906,5,203,Pierre Robin syndrome with fetal chondrodysplasia,C535776,3,1
0.099157906,5,203,Tennis Elbow,D013716,3,1
0.099157906,5,203,"Osteogenesis Imperfecta, Type V",C567042,3,1
0.099157906,5,203,Nocturia,D053158,3,1
0.099157906,5,203,"ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 5 (disorder)",C565776,3,1
0.099157906,5,203,Joint Instability,D007593,3,1
0.099157906,5,203,"Neuropathy, Hereditary Sensory And Autonomic, Type IIB",C567738,3,1
0.099157906,5,203,"Pain, Intractable",D010148,3,1
0.099157906,5,203,Feeding behaviors,D005247,3,1
0.099157906,5,203,"Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux",C564296,3,1
0.099157906,5,203,"Connective tissue nevus, NOS",C562737,3,1
0.099157906,5,203,"Epidermolysis bullosa, pretibial",C535494,3,1
0.099157906,5,203,Fasciitis,D005208,3,1
0.099157906,5,203,"Neuropathy, Hereditary Sensory, X-Linked",C564090,3,1
0.099157906,5,203,"Hematuria, Benign Familial",C562476,3,1
0.099157906,5,203,Lipodermatosclerosis,C537026,3,1
0.099157906,5,203,"Neuropathy, Hereditary Sensory, Atypical",C564946,3,1
0.099157906,5,203,Retrograde amnesia,D000648,3,1
0.276574057,4,221,Cognition,D003071,44,1
0.260616567,4,215,Paranoia,D010259,29,1
0.276574057,4,221,Bulimia,D002032,28,1
0.34163716,4,245,Precocious Puberty,C538542,62,1
0.30621277,4,232,Nail Diseases,D009260,39,1
0.31980276,4,237,Idiopathic generalized epilepsy,C562694,46,1
0.26591611,4,217,Pelger-Huet Anomaly,D010381,23,1
0.273902621,4,220,Spina Bifida Occulta,D016136,25,1
0.330709562,4,241,Tachycardia,D013610,49,1
0.30350207,4,231,"EAR, PATELLA, SHORT STATURE SYNDROME",C538012,35,1
0.093059722,5,199,"Microcoria, congenital",C537550,2,1
0.355312065,4,250,Cakut,C566906,65,1
0.26591611,4,217,"Pseudohypoparathyroidism, Type Ia",D011547,22,1
0.30350207,4,231,Ventricular Fibrillation,D014693,34,1
0.260616567,4,215,"Asthma, Occupational",D059366,20,1
0.094565623,5,200,Chromosome 18p deletion syndrome,C538309,2,1
0.322527004,4,238,Hypopituitarism,D007018,41,1
0.250082926,4,211,Rift Valley Fever,D012295,17,1
0.368988073,4,255,Hypopigmentation disorder,D017496,68,1
0.34163716,4,245,Pituitary-dependent Cushing's disease,D047748,49,1
0.322527004,4,238,Cholestasis of pregnancy,C535932,39,1
0.096083989,5,201,Brittle Bone Disorder,C565842,2,1
0.333439872,4,242,Turcot syndrome (disorder),C536928,43,1
0.097614769,5,202,Marfan Syndrome type 2,C535911,2,1
0.097614769,5,202,"Ehlers-Danlos syndrome, cardiac valvular form",C536200,2,1
0.097614769,5,202,"Alport syndrome, dominant type",C536586,2,1
0.097614769,5,202,Letterer-Siwe Disease,C538636,2,1
0.097614769,5,202,Keratoconus 1,C563649,2,1
0.097614769,5,202,Bruck syndrome 2,C537407,2,1
0.097614769,5,202,"Cardiac valvular dysplasia, X-linked",C535576,2,1
0.097614769,5,202,Hemorrhagic hereditary nephritis,D009394,2,1
0.097614769,5,202,Intervertebral Disk Displacement,D007405,2,1
0.097614769,5,202,"Alport syndrome, recessive type",C536587,2,1
0.097614769,5,202,Bruck syndrome 1,C537406,2,1
0.097614769,5,202,"Limb-girdle muscular dystrophy, type 2E",C535902,2,1
0.097614769,5,202,Geroderma osteodysplastica,C537799,2,1
0.097614769,5,202,Hypochondrogenesis,C563007,2,1
0.097614769,5,202,"ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 2",C563409,2,1
0.097614769,5,202,"Cutis Laxa, Autosomal Recessive, Type IIB",C567855,2,1
0.097614769,5,202,Megaepiphyseal dwarfism,C536140,2,1
0.097614769,5,202,"Short Stature, Idiopathic, Autosomal",C565805,2,1
0.097614769,5,202,"Larsen syndrome, dominant type",C537873,2,1
0.097614769,5,202,"Spondylometaphyseal dysplasia, 'corner fracture' type",C535793,2,1
0.097614769,5,202,Oculomelic amyoplasia,C537737,2,1
0.097614769,5,202,"Isolated Growth Hormone Deficiency, Type IB",C567564,2,1
0.097614769,5,202,"Ehlers-Danlos syndrome, type 3 (disorder)",C536196,2,1
0.097614769,5,202,Beta-sarcoglycanopathy,C535435,2,1
0.097614769,5,202,Perniola Krajewska Carnevale syndrome,C536660,2,1
0.097614769,5,202,Epidermolysis Bullosa Simplex With Pyloric Atresia,C567408,2,1
0.097614769,5,202,"STICKLER SYNDROME, TYPE II (disorder)",C537493,2,1
0.247464119,4,210,Myoclonic dystonia,C536096,15,1
0.37172194,4,256,Kallmann Syndrome,D017436,63,1
0.368988073,4,255,Addison Disease,D000224,60,1
0.271235709,4,219,Oculo-dento-digital syndrome,C563160,19,1
0.260616567,4,215,Heart murmur,D006337,16,1
0.404434206,4,268,Panic Disorder,D016584,80,1
0.239645427,4,207,"Affective Disorders, Psychotic",D000341,12,1
0.434147451,4,279,Xeroderma Pigmentosum,D014983,89,1
0.242245201,4,208,Prenatal Exposure Delayed Effects,D011297,11,1
0.242245201,4,208,Pemphigus and fogo selvagem,C535551,11,1
0.244851488,4,209,Ataxia with vitamin E deficiency,C535393,11,1
0.460806791,4,289,Microstomia,D008865,102,1
0.239645427,4,207,"Gambling, Pathological",D005715,10,1
0.479214225,4,296,Polyhydramnios,D006831,118,1
0.242245201,4,208,"MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 3 (disorder)",C563933,10,1
0.244851488,4,209,Lecithin Acyltransferase Deficiency,D007863,10,1
0.492214861,4,301,Cholelithiasis,D002769,119,1
0.244851488,4,209,Hyperlipoproteinemia Type IV,D006953,9,1
0.242245201,4,208,Neuroleptic Malignant Syndrome,D009459,8,1
0.229314843,4,203,Stuttering,D013342,7,1
0.234466093,4,205,Rumination Disorders,D019959,7,1
0.226750174,4,202,"Schizophrenia, Catatonic",D012560,6,1
0.602194595,4,346,Ciliopathies,D000072661,165,1
0.234466093,4,205,anaphylaxis,D000707,6,1
0.234466093,4,205,"PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC",C563422,6,1
0.234466093,4,205,Retinal Neovascularization,D015861,6,1
0.234466093,4,205,Chylomicron retention disease,C535460,6,1
0.237052335,4,206,Arcus Senilis,D001112,6,1
0.229314843,4,203,Slipped Capital Femoral Epiphyses,D060048,5,1
0.231886873,4,204,Expressed Emotion,D019260,5,1
0.231886873,4,204,Sea-Blue Histiocyte Syndrome,D012618,5,1
0.231886873,4,204,Hypertriglyceridemic Waist,D064250,5,1
0.231886873,4,204,Hyperkeratosis of the palms and soles and esophageal papillomas,C538682,5,1
0.774879244,5,534,Retinitis Pigmentosa,D012174,375,1
0.234466093,4,205,HMG CoA lyase deficiency,C538324,5,1
0.508107391,3,224,Ascites,D001201,42,1
0.531708787,3,232,Congenital neurologic anomalies,D009421,50,1
0.096083989,5,201,Palmoplantar Keratoderma with Deafness,C536152,1,1
0.096083989,5,201,"OTOPALATODIGITAL SYNDROME, TYPE II",C538089,1,1
0.096083989,5,201,Pericardial constriction with growth failure,C538604,1,1
0.096083989,5,201,Growth Hormone Deficiency With Pituitary Anomalies,C567632,1,1
0.096083989,5,201,Auditory Perceptual Disorders,D001308,1,1
0.096083989,5,201,Inosine Triphosphatase Deficiency,C564127,1,1
0.096083989,5,201,Kuskokwim disease,C538124,1,1
0.096083989,5,201,Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails,C562638,1,1
0.096083989,5,201,"Epiphyseal dysplasia, multiple, 1",C535501,1,1
0.096083989,5,201,Incisional hernia,D000069290,1,1
0.096083989,5,201,Fairbank disease,C536393,1,1
0.096083989,5,201,Masseter Muscle Spasm,D014313,1,1
0.096083989,5,201,Spondyloperipheral dysplasia short ulna,C535799,1,1
0.096083989,5,201,"AORTIC ANEURYSM, FAMILIAL ABDOMINAL 1",C565230,1,1
0.096083989,5,201,Malignant Atrophic Papulosis,D054853,1,1
0.096083989,5,201,"CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 2",C565176,1,1
0.096083989,5,201,Vertebral Artery Dissection,D020217,1,1
0.096083989,5,201,"Stickler syndrome, type 3",C537494,1,1
0.096083989,5,201,RETINITIS PIGMENTOSA 41 (disorder),C567422,1,1
0.096083989,5,201,Otopalatodigital Spectrum Disorder,C567577,1,1
0.096083989,5,201,Synostosis of Talus and Calcaneus with Short Stature,C566089,1,1
0.096083989,5,201,"Osteogenesis imperfecta, type 1A",C536041,1,1
0.096083989,5,201,Congenital myasthenic syndrome ib,C536089,1,1
0.096083989,5,201,Acholinesterasemia,C566750,1,1
0.096083989,5,201,"MYASTHENIA, FAMILIAL INFANTILE, 1",C565289,1,1
0.096083989,5,201,"ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS",C566528,1,1
0.096083989,5,201,"DIABETES MELLITUS, TRANSIENT NEONATAL, 2 (disorder)",C563672,1,1
0.096083989,5,201,Vitreoretinopathy with Phalangeal Epiphyseal Dysplasia,C565179,1,1
0.096083989,5,201,"Acrogeria, gottron type",C538187,1,1
0.096083989,5,201,Microcephalic Osteodysplastic Primordial Dwarfism with Tooth Abnormalities,C565898,1,1
0.096083989,5,201,"Mental Retardation, X-Linked, With Panhypopituitarism",C567485,1,1
0.096083989,5,201,"DEAFNESS, AUTOSOMAL RECESSIVE 49",C565717,1,1
0.096083989,5,201,"Hypocholinesterasemia, Fluoride-Resistant, Japanese Type",C566751,1,1
0.096083989,5,201,"Stickler Syndrome, Type I, Nonsyndromic Ocular",C563709,1,1
0.096083989,5,201,"TOENAIL DYSTROPHY, ISOLATED",C564384,1,1
0.096083989,5,201,EDS VIIB,C565061,1,1
0.096083989,5,201,Marshall syndrome,C536025,1,1
0.096083989,5,201,Kowarski syndrome,C537505,1,1
0.096083989,5,201,"Nephrotic Syndrome, Congenital, With Ocular Abnormalities And Congenital Myasthenic Syndrome",C537185,1,1
0.096083989,5,201,Achondrogenesis type 2,C536017,1,1
0.096083989,5,201,Laryngoonychocutaneous syndrome,C537032,1,1
0.096083989,5,201,Narcotic Dependence,D009294,1,1
0.096083989,5,201,"Prolactin Deficiency, Isolated",C562708,1,1
0.096083989,5,201,CONE-ROD DYSTROPHY 12 (disorder),C567206,1,1
0.096083989,5,201,Encephaloclastic Proliferative Vasculopathy,C565593,1,1
0.096083989,5,201,"Syncope, Effort",D013575,1,1
0.096083989,5,201,Corneal edema,D015715,1,1
0.096083989,5,201,"Epilepsy, Nocturnal Frontal Lobe, Type 3",C565334,1,1
0.096083989,5,201,OI-EDS Combined Syndrome,C565178,1,1
0.096083989,5,201,"Pancreatic cancer, adult",C535836,1,1
0.096083989,5,201,"Platyspondylic Lethal Skeletal Dysplasia, Torrance Type",C563627,1,1
0.096083989,5,201,"Myasthenic syndrome, congenital, postsynaptic slow-channel",C536091,1,1
0.096083989,5,201,"Epilepsy, Nocturnal Frontal Lobe, Type 4",C563679,1,1
0.096083989,5,201,"SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE",C564794,1,1
0.096083989,5,201,Asymptomatic Infections,D058345,1,1
0.096083989,5,201,"Atelosteogenesis, type 1",C535396,1,1
0.096083989,5,201,"CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 3 (disorder)",C563788,1,1
0.096083989,5,201,"Factor Xiii, A Subunit, Deficiency Of",C567691,1,1
0.096083989,5,201,"CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 6",C567675,1,1
0.096083989,5,201,"Ichthyosis, Nonlamellar and Nonerythrodermic, Congenital, Autosomal Recessive",C565749,1,1
0.096083989,5,201,"Catatonia, Malignant",D002389,1,1
0.096083989,5,201,Phimosis,D010688,1,1
0.096083989,5,201,Epidermolysis Bullosa Simplex Superficialis,C564368,1,1
0.096083989,5,201,"Hearing Loss, Bilateral",D006312,1,1
0.096083989,5,201,Verloes Bourguignon syndrome,C536538,1,1
0.096083989,5,201,GEMSS syndrome,C537679,1,1
0.096083989,5,201,"ARTHROGRYPOSIS, DISTAL, TYPE 10",C566069,1,1
0.096083989,5,201,Arthrogryposis-like hand anomaly and sensorineural deafness,C535386,1,1
0.096083989,5,201,Bull's eye macular dystrophy,C562746,1,1
0.096083989,5,201,Fitzsimmons-Guilbert syndrome,C537938,1,1
0.096083989,5,201,"EPIPHYSEAL DYSPLASIA, MULTIPLE, 5",C535505,1,1
0.096083989,5,201,"Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency",C564317,1,1
0.096083989,5,201,"CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 4",C567677,1,1
0.096083989,5,201,"Osteogenesis imperfecta, type 5",C536046,1,1
0.096083989,5,201,"Czech dysplasia, metatarsal type",C535766,1,1
0.096083989,5,201,Epidermolysis Bullosa Dystrophica With Subcorneal Cleavage,C567272,1,1
0.096083989,5,201,"Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency",C567709,1,1
0.096083989,5,201,"NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 2",C566869,1,1
0.096083989,5,201,Infectious Canine Hepatitis,D006522,1,1
0.096083989,5,201,Panhypopituitarism - X-linked,C538613,1,1
0.096083989,5,201,"DEAFNESS, AUTOSOMAL RECESSIVE 77 (disorder)",C567543,1,1
0.096083989,5,201,Brain Small Vessel Disease With Axenfeld-Rieger Anomaly,C564372,1,1
0.096083989,5,201,"ARTHROGRYPOSIS, DISTAL, TYPE 4 (disorder)",C563791,1,1
0.096083989,5,201,"Genetic Diseases, X-Linked",D040181,1,1
0.096083989,5,201,"Upper Extremity Deep Vein Thrombosis, Primary",D056824,1,1
0.096083989,5,201,Terminal Osseous Dysplasia and Pigmentary Defects,C564554,1,1
0.096083989,5,201,"Epidermolysis bullosa simplex, Ogna type",C535962,1,1
0.096083989,5,201,Osteoarthritis with Mild Chondrodysplasia,C565740,1,1
0.096083989,5,201,Lens Subluxation,D007906,1,1
0.096083989,5,201,"Heterotopia, Periventricular Nodular, with Frontometaphyseal Dysplasia",C564725,1,1
0.096083989,5,201,Osteogenesis Imperfecta Type VII,C565200,1,1
0.096083989,5,201,"Osteogenesis imperfecta, type 7",C536048,1,1
0.096083989,5,201,Stiff Skin Syndrome,C566112,1,1
0.096083989,5,201,"ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 1 (disorder)",C566254,1,1
0.096083989,5,201,"Tooth Agenesis, Selective, 6",C567755,1,1
0.096083989,5,201,Submandibular Gland Diseases,D013364,1,1
0.096083989,5,201,Hypopituitarism and septooptic 'dysplasia',C531815,1,1
0.096083989,5,201,"Osteogenesis imperfecta, type VIII",C536049,1,1
0.096083989,5,201,"Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness",C565046,1,1
0.096083989,5,201,"Myosclerosis, Autosomal Recessive",C564968,1,1
0.096083989,5,201,Transient bullous dermolysis of the newborn,C536979,1,1
0.096083989,5,201,"MENTAL RETARDATION, EPILEPTIC SEIZURES, HYPOGONADISM AND HYPOGENITALISM, MICROCEPHALY, AND OBESITY (disorder)",C537451,1,1
0.096083989,5,201,"RHEGMATOGENOUS RETINAL DETACHMENT, AUTOSOMAL DOMINANT",C563710,1,1
0.096083989,5,201,"Knuckle pads, leuconychia and sensorineural deafness",C537210,1,1
0.096083989,5,201,"Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related",C563869,1,1
0.096083989,5,201,"Epilepsy, Nocturnal Frontal Lobe, Type 1",C563930,1,1
0.096083989,5,201,Marfanoid hypermobility syndrome,C531742,1,1
0.096083989,5,201,Scleredema Adultorum,D012592,1,1
0.096083989,5,201,"MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 9 (disorder)",C567393,1,1
0.096083989,5,201,Pituitary Dwarfism Type 3,C563172,1,1
0.096083989,5,201,CAMPOMELIC DYSPLASIA WITH AUTOSOMAL SEX REVERSAL,C564282,1,1
0.096083989,5,201,Cortical Congenital Hyperostosis,D006958,1,1
0.096083989,5,201,Boomerang dysplasia,C536573,1,1
0.096083989,5,201,Congenital hypertrichosis lanuginosa,C538389,1,1
0.096083989,5,201,Frontootopalatodigital Osteodysplasia,C567578,1,1
0.096083989,5,201,"DEAFNESS, AUTOSOMAL DOMINANT 3A (disorder)",C567277,1,1
0.096083989,5,201,"Hypoglycemia, leucine-induced",C537150,1,1
0.096083989,5,201,Familial vascular leukoencephalopathy,C531642,1,1
0.096083989,5,201,"Plantar Lipomatosis, Unusual Facies, and Developmental Delay",C566559,1,1
0.096083989,5,201,"Multiple Pterygium Syndrome, Autosomal Dominant",C566739,1,1
0.096083989,5,201,Congenital idiopathic intestinal pseudoobstruction,C535532,1,1
0.096083989,5,201,"Mental Retardation, X-Linked, with Isolated Growth Hormone Deficiency",C564712,1,1
0.096083989,5,201,Kyphomelic dysplasia,C538128,1,1
0.096083989,5,201,"Skeletal Defects, Genital Hypoplasia, And Mental Retardation",C567306,1,1
0.096083989,5,201,"DEAFNESS, AUTOSOMAL RECESSIVE 42 (disorder)",C566460,1,1
0.096083989,5,201,"EPIPHYSEAL DYSPLASIA, MULTIPLE, 3",C535503,1,1
0.096083989,5,201,"Heterotopia, Periventricular, Ehlers-Danlos Variant",C564492,1,1
0.096083989,5,201,Hernia of abdominal cavity,D046449,1,1
0.096083989,5,201,Endocrine-Cerebroosteodysplasia,C567210,1,1
0.096083989,5,201,Penttinen-Aula syndrome,C536653,1,1
0.096083989,5,201,Feminization,D005262,1,1
0.096083989,5,201,"Dominant dystrophic epidermolysis bullosa, albopapular type (disorder)",C535956,1,1
0.096083989,5,201,"Filaminopathy, autosomal dominant",C537932,1,1
0.096083989,5,201,Glycoprotein IA Deficiency,C566000,1,1
0.096083989,5,201,Familial mesangial sclerosis,C537346,1,1
0.096083989,5,201,Boerhaave syndrome,C536571,1,1
0.096083989,5,201,"Arthrogryposis, distal, type 2E",C535384,1,1
0.096083989,5,201,Atelosteogenesis Type 3,C579928,1,1
0.096083989,5,201,Atrial Septal Defect 6,C567764,1,1
0.096083989,5,201,"Spondylometaphyseal dysplasia, Algerian type",C535794,1,1
0.096083989,5,201,"Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps",C567088,1,1
0.646840175,3,275,Hydronephrosis,D006869,105,1
0.51703053,3,227,FRAGILE X TREMOR/ATAXIA SYNDROME,C564105,40,1
0.226750174,4,202,Weill-Marchesani-Like Syndrome,C567710,4,1
0.226750174,4,202,Arteriolosclerosis,D050379,4,1
0.78863634,3,345,Body Height,D001827,265,1
0.668249277,3,284,Pervasive Development Disorder,D002659,112,1
0.641952987,3,273,Polyneuropathy,D011115,92,1
0.229314843,4,203,Neck Pain,D019547,4,1
0.677457547,3,288,"Hernia, Inguinal",D006552,115,1
0.582412835,3,250,Nausea,D009325,57,1
0.546136251,3,237,Amenorrhea,D000568,44,1
0.574204044,3,247,Nijmegen Breakage Syndrome,D049932,53,1
0.231886873,4,204,"THYROID HORMONE RESISTANCE, GENERALIZED, AUTOSOMAL DOMINANT",C567934,4,1
0.231886873,4,204,"Thyroid Hormone Resistance, Generalized, Autosomal Recessive",C567936,4,1
0.231886873,4,204,Adolescent Obesity,D063766,4,1
0.231886873,4,204,Emotional Disturbances,D000342,4,1
0.231886873,4,204,ICHTHYOSIS EXFOLIATIVA,C563978,4,1
0.231886873,4,204,"Peroxisome Biogenesis Disorder, Complementation Group G",C566406,4,1
0.231886873,4,204,Carnitine palmitoyl transferase 1A deficiency,C535588,4,1
0.231886873,4,204,Familial hyperchylomicronemia syndrome,C538489,4,1
0.231886873,4,204,Epidermolysis bullosa simplex with mottled pigmentation,C535959,4,1
0.231886873,4,204,Ichthyosis Vulgaris,D016112,4,1
0.546136251,3,237,Panhypopituitarism,C580003,43,1
0.710311171,3,303,Myoclonus,D009207,136,1
0.563105598,3,243,Hypercalciuria,D053565,48,1
0.619381004,3,264,"Cardiomyopathy, Hypertrophic, Familial",D024741,71,1
0.644402459,3,274,Premature aging syndrome,D019588,82,1
0.65647329,3,279,Leigh Disease,D007888,89,1
0.546136251,3,237,"Skin Diseases, Genetic",D012873,41,1
0.508107391,3,224,Cataplexy,D002385,31,1
0.675173187,3,287,Borderline Personality Disorder,D001883,99,1
0.51406566,3,226,Rickets,D012279,32,1
0.496079334,3,220,Cartilage-hair hypoplasia,C535916,26,1
0.502111695,3,222,"Pain, Postoperative",D010149,27,1
0.486963798,3,217,Hiatal Hernia,D006551,24,1
0.809035643,3,358,Constipation,D003248,192,1
0.810534255,3,359,Brachydactyly,D059327,192,1
0.490011104,3,218,Heart Block,D006327,23,1
0.505114175,3,223,Hypersomnia,D006970,25,1
0.490011104,3,218,Hunger,D006815,22,1
0.483907839,3,216,Tooth Attrition,D019217,21,1
0.820750224,3,366,Ataxia,D001259,188,1
0.480843338,3,215,Conduct Disorder,D019955,20,1
0.986729869,3,655,Cerebellar Ataxia,D002524,503,1
0.824983825,3,369,Vomiting,D014839,180,1
0.483907839,3,216,Mucopolysaccharidosis Type IIIA,D009084,20,1
0.884877806,3,420,"Infant, Small for Gestational Age",D007236,258,1
0.224193037,4,201,FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1B,C563557,3,1
0.999377111,1,598,Nystagmus,D009759,462,1
0.226750174,4,202,"Weill-Marchesani Syndrome, Autosomal Dominant",D056846,3,1
0.226750174,4,202,Knobloch syndrome,C537209,3,1
0.477770406,3,214,Thyrotoxicosis,D013971,17,1
0.229314843,4,203,Musculoskeletal Pain,D059352,3,1
0.229314843,4,203,"Hdl Deficiency, Type 2",C538394,3,1
0.229314843,4,203,LIPOPROTEIN GLOMERULOPATHY,C567089,3,1
0.229314843,4,203,Cardiotoxicity,D066126,3,1
0.229314843,4,203,"Hypobetalipoproteinemia, Familial, 2",C565732,3,1
0.853998421,2,280,Intelligence,D007360,173,1
0.474689158,3,213,Rokitansky Kuster Hauser syndrome,C537371,16,1
0.998279708,1,517,Strabismus,D013285,384,1
0.465396696,3,210,Globoid cell leukodystrophy,D007965,15,1
0.468502183,3,211,T-Lymphocytopenia,C536783,15,1
0.981603265,2,484,Optic Atrophy,D009896,327,1
0.867292817,2,290,Smoking Behaviors,D012907,165,1
0.462283373,3,209,"Phobia, Social",D000072861,14,1
0.465396696,3,210,child abuse behavior,D002649,14,1
0.99653807,1,461,Blepharoptosis,D001763,315,1
0.471599711,3,212,Cancer Pain,D000072716,14,1
0.945567365,2,380,Microcephaly,D008831,221,1
0.474689158,3,213,Niemann-Pick Diseases,D009542,14,1
0.932678049,2,359,Microphthalmos,D008850,200,1
0.477770406,3,214,Waxy flexibility,D002375,14,1
0.468502183,3,211,Familial Exudative Vitreoretinopathy,C580083,13,1
0.474689158,3,213,Brachydactyly type A3,C537090,13,1
0.802984589,2,248,Bone Density,D015519,85,1
0.992786263,1,402,Low Vision,D015354,243,1
0.871060124,2,293,Dystonia Disorders,D020821,121,1
0.99152272,1,389,Visual Impairment,D014786,233,1
0.92331104,2,346,"Acidosis, Lactic",D000140,158,1
0.858108635,2,283,Polymicrogyria,D065706,102,1
0.462283373,3,209,Dysthymic Disorder,D019263,11,1
0.826993563,2,262,Retinal Degeneration,D012162,84,1
0.878302613,2,299,Lethargy,D053609,107,1
0.985375318,1,345,Neurodevelopmental Disorders,D065886,183,1
0.786036308,2,239,Arachnodactyly,D054119,62,1
0.825369467,2,261,Conduction disorder of the heart,D000075224,76,1
0.826993563,2,262,Lysosomal Storage Diseases,D016464,73,1
0.981728021,1,327,Retinal Dystrophies,D058499,162,1
0.828604128,2,263,Bloom Syndrome,D001816,72,1
0.818736011,2,257,Inborn Errors of Metabolism,D008661,67,1
0.968543596,1,283,Platelet mean volume determination (procedure),D063847,145,1
0.982393358,1,330,Azoospermia,D053713,153,1
0.787980575,2,240,Urinary Incontinence,D014549,54,1
0.815335796,2,255,"Optic Atrophy, Hereditary, Leber",D029242,61,1
0.456033729,3,207,PARIETAL FORAMINA,C566826,9,1
0.791822731,2,242,Heart Septal Defects,D006343,53,1
0.981037672,1,324,Polydactyly,D017689,139,1
0.799324026,2,246,Bardet-Biedl Syndrome,D020788,55,1
0.804792661,2,249,Nephrocalcinosis,D009397,55,1
0.786036308,2,239,Bradycardia,D001919,49,1
0.786036308,2,239,"Amaurosis congenita of Leber, type 1",C536600,48,1
0.974494563,1,300,Cardiac Arrhythmia,D001145,123,1
0.769913991,2,231,Congenital absence of germinal epithelium of testes,D054331,43,1
0.976315437,1,306,Hyperammonemia,D022124,118,1
0.791822731,2,242,"Tachycardia, Ventricular",D017180,47,1
0.782100955,2,237,"Mental Retardation, X-Linked 1",C567906,44,1
0.452897666,3,206,Bladder Exstrophy,D001746,8,1
0.793720799,2,243,Congenital adrenal hyperplasia,D000312,46,1
0.226750174,4,202,"Erythrokeratoderma, Reticular",C563781,2,1
0.226750174,4,202,Cardiac Death,D003643,2,1
0.226750174,4,202,"Macrothrombocytopenia-Stomatocytosis, Mediterranean",C537345,2,1
0.226750174,4,202,Psychological Trauma,D000067073,2,1
0.226750174,4,202,"Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis",C564367,2,1
0.226750174,4,202,Peptic Ulcer Hemorrhage,D010438,2,1
0.226750174,4,202,"Epidermolytic Hyperkeratosis, Late-Onset",C566187,2,1
0.226750174,4,202,"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)",C566968,2,1
0.226750174,4,202,"Muscular Dystrophy, Animal",D009137,2,1
0.226750174,4,202,Post-Concussion Syndrome,D038223,2,1
0.226750174,4,202,Blepharophimosis syndrome Ohdo type,C536232,2,1
0.226750174,4,202,Lipase deficiency combined,C535904,2,1
0.226750174,4,202,"SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE",C536787,2,1
0.226750174,4,202,Mutilating keratoderma,C536457,2,1
0.226750174,4,202,"THYROID HORMONE RESISTANCE, SELECTIVE PITUITARY",C564154,2,1
0.778102586,2,235,Hyponatremia,D007010,41,1
0.759311332,2,226,Eye Abnormalities,D005124,37,1
0.963529579,1,271,Macrostomia,D008265,98,1
0.942497061,1,234,Waist-Hip Ratio,D049629,88,1
0.780109691,2,236,Flushing,D005483,40,1
0.956667098,1,257,Enophthalmos,D015841,94,1
0.437110367,3,201,FG syndrome,C537923,7,1
0.759311332,2,226,Infection by Cryptococcus neoformans,D003453,36,1
0.761464939,2,227,Cerebellar Diseases,D002526,36,1
0.963529579,1,271,Kartagener Syndrome,D007619,95,1
0.759311332,2,226,Dyskeratosis Congenita,D019871,35,1
0.761464939,2,227,Adrenal gland hypofunction,D000309,34,1
0.754953907,2,224,Malignant neoplasm of pharynx,D010610,32,1
0.449754288,3,205,Postoperative Nausea and Vomiting,D020250,7,1
0.748290978,2,221,Generalized elastolysis,C531660,30,1
0.456033729,3,207,Premenstrual Dysphoric Disorder,D065446,7,1
0.456033729,3,207,Disruptive Behavior Disorder,D019958,7,1
0.748290978,2,221,Gilbert Disease (disorder),D005878,29,1
0.748290978,2,221,Hyperphagia,D006963,28,1
0.743763525,2,219,Pulmonary artery stenosis,D000071079,27,1
0.759311332,2,226,Congenital adrenal hyperplasia due to 21 hydroxylase deficiency,C535979,29,1
0.75274992,2,223,Exostoses,D005096,28,1
0.761464939,2,227,Polydipsia,D059606,29,1
0.962619815,1,269,Comatose,D003128,72,1
0.757141016,2,225,Seasonal Affective Disorder,D016574,28,1
0.757141016,2,225,Bunion,D000071378,28,1
0.759311332,2,226,Meckel syndrome type 1,C536133,28,1
0.712620648,2,206,Longevity,D008136,22,1
0.759311332,2,226,Open Bite,D024343,27,1
0.73684245,2,216,ATRIOVENTRICULAR CANAL DEFECT,C562831,24,1
0.959752812,1,263,"Neoplastic Syndromes, Hereditary",D009386,65,1
0.950385975,1,246,Glycogen storage disease type II,D006009,62,1
0.446603729,3,204,Amelogenesis Imperfecta hypomaturation type,C536606,6,1
0.952768462,1,250,Long QT Syndrome,D008133,62,1
0.750528972,2,222,Septo-Optic Dysplasia,D025962,25,1
0.950992577,1,247,alpha-Thalassemia,D017085,61,1
0.452897666,3,206,Pseudoainhum,C535821,6,1
0.452897666,3,206,Limb-girdle muscular dystrophy type 2H,C535897,6,1
0.949771902,1,245,Disorders of Sex Development,D012734,58,1
0.743763525,2,219,Parathyroid Diseases,D010279,23,1
0.947239059,1,241,"Paraparesis, Spastic",D020336,54,1
0.942497061,1,234,Obsessive compulsive behavior,D003192,51,1
0.750528972,2,222,Hemianopsia,D006423,22,1
0.94788394,1,242,Anophthalmos,D000853,50,1
0.722524751,2,210,Clubbed Fingers,D010005,19,1
0.724955589,2,211,Timothy syndrome,C536962,19,1
0.94788394,1,242,Channelopathies,D053447,48,1
0.734500463,2,215,Nonketotic Hyperglycinemia,D020158,19,1
0.73684245,2,216,Sprengel deformity,C535802,19,1
0.942497061,1,234,Hypocalcemia,D006996,45,1
0.947239059,1,241,"Xeroderma Pigmentosum, Complementation Group D",C562591,45,1
0.729763567,2,213,Isodicentric Chromosome 15 Syndrome,C580205,18,1
0.732140861,2,214,Hereditary Multiple Exostoses,D005097,18,1
0.446603729,3,204,Extravasation of Diagnostic and Therapeutic Materials,D005119,5,1
0.446603729,3,204,Unconscious State,D014474,5,1
0.94788394,1,242,Cafe-au-Lait Spots,D019080,43,1
0.724955589,2,211,Teratozoospermia,D000072660,17,1
0.724955589,2,211,"Jaundice, Obstructive",D041781,17,1
0.939599379,1,230,Choanal Atresia,D002754,41,1
0.943893601,1,236,"Limb Deformities, Congenital",D017880,41,1
0.938096513,1,228,Telangiectasis,D013684,40,1
0.938096513,1,228,Chronic progressive external ophthalmoplegia,D017246,40,1
0.732140861,2,214,Aortopulmonary Septal Defect,D001028,17,1
0.940337142,1,231,Glycosuria,D006029,38,1
0.934978258,1,224,Unilateral agenesis of kidney,D000075529,37,1
0.941785875,1,233,Paranasal Sinus Diseases,D010254,38,1
0.939599379,1,230,Testicular hypogonadism,D005058,36,1
0.722524751,2,210,Skin Pigmentation,D012880,15,1
0.729763567,2,213,UV-Sensitive Syndrome,C563466,15,1
0.934978258,1,224,Intrahepatic Cholestasis,D002780,33,1
0.720075913,2,209,Osteoblastoma,D018215,14,1
0.930859807,1,219,Atrioventricular Block,D054537,32,1
0.722524751,2,210,Stiff-Person Syndrome,D016750,14,1
0.722524751,2,210,Congenital absence of kidneys syndrome,C536482,14,1
0.925573746,1,213,Congenital malrotation of intestine,C562456,31,1
0.934978258,1,224,Coxa valga,D060906,32,1
0.936556445,1,226,Intracranial Hypertension,D019586,32,1
0.931703752,1,220,Amblyopia,D000550,31,1
0.933361015,1,222,Iron-Refractory Iron Deficiency Anemia,C562385,31,1
0.729763567,2,213,Lesch-Nyhan Syndrome,D007926,14,1
0.729763567,2,213,Infantile Neuroaxonal Dystrophy,D019150,14,1
0.925573746,1,213,CHARGE Syndrome,D058747,30,1
0.712620648,2,206,Testicular Diseases,D013733,13,1
0.930859807,1,219,DOWN SYNDROME CRITICAL REGION,C566023,30,1
0.935772175,1,225,Exocrine pancreatic insufficiency,D010188,30,1
0.932537447,1,221,Bartter Disease,D001477,29,1
0.923723855,1,211,Metatarsus Varus,D000070592,28,1
0.92465445,1,212,Mean blood pressure,D062186,28,1
0.724955589,2,211,Hypoventilation,D007040,13,1
0.727368503,2,212,Hypovolemia,D020896,13,1
0.930005487,1,218,Unverricht-Lundborg Syndrome,D020194,28,1
0.729763567,2,213,Robinow Syndrome,C562492,13,1
0.933361015,1,222,MELAS Syndrome,D017241,28,1
0.934174578,1,223,"Preauricular Fistulae, Congenital",C563015,28,1
0.446603729,3,204,Odontogenesis Imperfecta,D018126,4,1
0.936556445,1,226,Glycogen Storage Disease,D006008,28,1
0.936556445,1,226,Methylmalonic acidemia,C537358,28,1
0.717608999,2,208,Quadriparesis,D011782,12,1
0.720075913,2,209,Pseudopseudohypoparathyroidism,D011556,12,1
0.724955589,2,211,Occupational Diseases,D009784,12,1
0.724955589,2,211,"Anemia, Hemolytic, Congenital",D000745,12,1
0.934174578,1,223,ULNAR HYPOPLASIA,C538069,26,1
0.927378991,1,215,Blepharitis,D001762,25,1
0.930005487,1,218,Pierre Robin Syndrome,D010855,25,1
0.932537447,1,221,Febrile Neutropenia,D064147,25,1
0.934978258,1,224,Romano-Ward Syndrome,D029597,25,1
0.929140663,1,217,Mucopolysaccharidoses,D009083,24,1
0.717608999,2,208,Hypoparathyroidism - autosomal dominant,C562783,11,1
0.722524751,2,210,"CRANIOSYNOSTOSIS, TYPE 2",C565753,11,1
0.724955589,2,211,Foot Ulcer,D016523,11,1
0.928265208,1,216,Hallervorden-Spatz Syndrome,D006211,23,1
0.929140663,1,217,Echolalia,D004454,23,1
0.930859807,1,219,Hereditary spherocytosis,D013103,23,1
0.930859807,1,219,"Gonadal Dysgenesis, Mixed",D006060,23,1
0.707559116,2,204,Blood urea nitrogen measurement,D001806,10,1
0.927378991,1,215,"Hydrocephalus, Normal Pressure",D006850,22,1
0.930005487,1,218,Pendred's syndrome,C536648,22,1
0.930859807,1,219,Central Core Myopathy (disorder),D020512,22,1
0.931703752,1,220,Andersen Syndrome,D050030,22,1
0.932537447,1,221,"Ichthyosiform Erythroderma, Congenital",D016113,22,1
0.715123935,2,207,Supraventricular tachycardia,D013617,10,1
0.717608999,2,208,Female Genital Diseases,D005831,10,1
0.925573746,1,213,Episodic Ataxia,C580065,21,1
0.928265208,1,216,Platelet Storage Pool Deficiency,D010981,21,1
0.929140663,1,217,Neurodegeneration with brain iron accumulation (NBIA),C538421,21,1
0.929140663,1,217,Restrictive cardiomyopathy,D002313,21,1
0.930005487,1,218,Jeune thoracic dystrophy,C537571,21,1
0.930859807,1,219,Trichothiodystrophy Syndromes,D054463,21,1
0.918896529,1,206,"Schizophrenia, Childhood",D012561,20,1
0.922781826,1,210,Seborrheic dermatitis,D012628,20,1
0.926481882,1,214,Benign Rolandic Epilepsy,D019305,20,1
0.928265208,1,216,Urethral Stricture,D014525,20,1
0.929140663,1,217,Porphyria Cutanea Tarda,D017119,20,1
0.930005487,1,218,Gitelman Syndrome,D053579,20,1
0.930859807,1,219,Triphalangeal thumb,C573898,20,1
0.930859807,1,219,"ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)",C538261,20,1
0.91789519,1,205,"Myopia, Degenerative",D047728,19,1
0.926481882,1,214,"Amnesia, Transient Global",D020236,19,1
0.928265208,1,216,Torsades de Pointes,D016171,19,1
0.928265208,1,216,Irido-corneo-trabecular dysgenesis (disorder),C537884,19,1
0.717608999,2,208,Pilomatrixoma,D018296,9,1
0.717608999,2,208,Isolated lutropin deficiency (disorder),C537919,9,1
0.720075913,2,209,"POLYMICROGYRIA, BILATERAL FRONTOPARIETAL",C564652,9,1
0.922781826,1,210,Hair Color,D006200,18,1
0.927378991,1,215,22q11 Deletion Syndrome,D058165,18,1
0.927378991,1,215,"Amino Acid Metabolism, Inborn Errors",D000592,18,1
0.437110367,3,201,"Deafness, Autosomal Recessive 10",C565341,3,1
0.437110367,3,201,Alstrom Syndrome,D056769,3,1
0.929140663,1,217,Paraplegia,D010264,18,1
0.440281626,3,202,Progressive hearing loss stapes fixation,C536424,3,1
0.440281626,3,202,"Ectodermal Dysplasia, Pure Hair-Nail Type",C566592,3,1
0.440281626,3,202,Adrenal Cortex Diseases,D000303,3,1
0.440281626,3,202,"AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 1",C538243,3,1
0.921828221,1,209,Accessory nipple,C562557,17,1
0.443446128,3,203,Langer Mesomelic Dysplasia Syndrome,C537267,3,1
0.443446128,3,203,Miyoshi Muscular Dystrophy 3,C567645,3,1
0.443446128,3,203,"Pterygium, Antecubital",C566738,3,1
0.443446128,3,203,"HYPERPARATHYROIDISM, NEONATAL SEVERE",C563375,3,1
0.443446128,3,203,Hyperesthesia,D006941,3,1
0.92465445,1,212,Early onset torsion dystonia,C538005,17,1
0.928265208,1,216,Dysgraphia,D000381,17,1
0.710099065,2,205,Ossifying Fibroma,D018214,8,1
0.224193037,4,201,"Epilepsy, Simple Partial",D004828,1,1
0.224193037,4,201,MPTP Poisoning,D020267,1,1
0.224193037,4,201,Apolipoprotein C-III Deficiency,C566270,1,1
0.224193037,4,201,Hypoprebetalipoproteinemia,D007009,1,1
0.224193037,4,201,"MYOPATHY, DISTAL, WITH ANTERIOR TIBIAL ONSET",C564664,1,1
0.224193037,4,201,Keratoderma palmoplantaris transgrediens,C536154,1,1
0.224193037,4,201,"CARDIOMYOPATHY, DILATED, 1L",C564679,1,1
0.224193037,4,201,Keratosis palmoplantaris striata 3,C536163,1,1
0.224193037,4,201,"Psychoses, Alcoholic",D011604,1,1
0.224193037,4,201,NEUTROPHIL ACTIN DYSFUNCTION,C564942,1,1
0.224193037,4,201,"Encephalomyelitis, Western Equine",D020241,1,1
0.224193037,4,201,Heart Valve Prolapse,D016127,1,1
0.224193037,4,201,"Ventricular Outflow Obstruction, Left",D014694,1,1
0.224193037,4,201,"Hemorrhagic Septicemia, Viral",D031941,1,1
0.224193037,4,201,"Tsc2 Angiomyolipomas, Renal, Modifier Of",C567682,1,1
0.224193037,4,201,Clasp-Knife Spasticity,D009128,1,1
0.224193037,4,201,PREMATURE OVARIAN FAILURE 7 (disorder),C567838,1,1
0.224193037,4,201,Benign Paroxysmal Positional Vertigo,D065635,1,1
0.224193037,4,201,Ectopia Lentis with Ectopia of Pupil,C563268,1,1
0.224193037,4,201,"Lp(A) Deficiency, Congenital",C563618,1,1
0.224193037,4,201,"Ectopia Lentis, Isolated, Autosomal Recessive",C567124,1,1
0.224193037,4,201,"Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy",C565359,1,1
0.224193037,4,201,Orthomyxoviridae Infections,D009976,1,1
0.224193037,4,201,"Hypobetalipoproteinemia, Familial, Apolipoprotein B",D052476,1,1
0.224193037,4,201,Pellagra,D010383,1,1
0.224193037,4,201,Limb-girdle muscular dystrophy type 2F,C535896,1,1
0.224193037,4,201,GALLBLADDER DISEASE 4,C566936,1,1
0.224193037,4,201,"Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract",C567203,1,1
0.224193037,4,201,"Hyperchylomicronemia With Hyperprebetalipoproteinemia, Familial",D006954,1,1
0.224193037,4,201,GRACILE SYNDROME (disorder),C537934,1,1
0.224193037,4,201,Sleep Bruxism,D020186,1,1
0.224193037,4,201,"Ichthyosis hystrix, Curth Macklin type",C536088,1,1
0.224193037,4,201,"Deafness, Autosomal Dominant 2B",C567214,1,1
0.224193037,4,201,Binge eating disorder,D056912,1,1
0.224193037,4,201,Pinguecula,D059407,1,1
0.224193037,4,201,Krause-Kivlin syndrome,C537617,1,1
0.921828221,1,209,Odontogenesis,D009805,16,1
0.715123935,2,207,"Hypocalciuric hypercalcemia, familial, type 1",C537145,8,1
0.715123935,2,207,Cerebrooculofacioskeletal Syndrome 1,C562434,8,1
0.923723855,1,211,Tarsal Coalition,D000070604,16,1
0.926481882,1,214,Alkalosis,D000471,16,1
0.923723855,1,211,Mobius Syndrome,D020331,15,1
0.92465445,1,212,Diplopia,D004172,15,1
0.925573746,1,213,Kabuki make-up syndrome,C537705,15,1
0.926481882,1,214,Colon diverticulum anatomic structure,D004241,15,1
0.926481882,1,214,"Gonadal Dysgenesis, 46,XY",D006061,15,1
0.926481882,1,214,Diverticular disease of colon,D043963,15,1
0.926481882,1,214,Paroxysmal familial ventricular fibrillation,C537182,15,1
0.918896529,1,206,Partial agenesis of corpus callosum,C536111,14,1
0.922781826,1,210,"XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP E",C564732,14,1
0.92465445,1,212,Anovulation,D000858,14,1
0.925573746,1,213,SPINOCEREBELLAR ATAXIA 17,C564616,14,1
0.926481882,1,214,Cystic medial necrosis of aorta,C536230,14,1
0.926481882,1,214,"Nystagmus, End-Position",D009760,14,1
0.715123935,2,207,"TIBIAL MUSCULAR DYSTROPHY, TARDIVE",D049310,7,1
0.919885716,1,207,Tracheal Stenosis,D014135,13,1
0.920862899,1,208,Cyclocephaly,C562573,13,1
0.922781826,1,210,Limbic Encephalitis,D020363,13,1
0.922781826,1,210,Pertussis,D014917,13,1
0.922781826,1,210,Polydactyly preaxial type 1,C536332,13,1
0.923723855,1,211,Hereditary liability to pressure palsies,C536965,13,1
0.92465445,1,212,Natal Teeth,D009306,13,1
0.92465445,1,212,Congenital abnormal Synostosis,D013580,13,1
0.920862899,1,208,Congenital Foot Deformity,D005532,12,1
0.921828221,1,209,Otosclerosis,D010040,12,1
0.922781826,1,210,Oncogenic osteomalacia,C537751,12,1
0.923723855,1,211,Adrenal Gland Diseases,D000307,12,1
0.923723855,1,211,SPINOCEREBELLAR ATAXIA 8,C537307,12,1
0.70500073,2,203,Auriculo-condylar syndrome,C538270,6,1
0.707559116,2,204,Generalized Myotonia of Thomsen,D009224,6,1
0.710099065,2,205,OSSIFICATION OF THE POSTERIOR LONGITUDINAL LIGAMENT OF SPINE,C537143,6,1
0.712620648,2,206,"ACTH Syndrome, Ectopic",D000182,6,1
0.91688155,1,204,"Tooth, Supernumerary",D014096,11,1
0.91789519,1,205,Patellar Dislocation,D031222,11,1
0.91789519,1,205,Kleine-Levin Syndrome,D017593,11,1
0.91789519,1,205,Freeman-Sheldon syndrome,C535483,11,1
0.918896529,1,206,Jacobsen Distal 11q Deletion Syndrome,D054868,11,1
0.918896529,1,206,Atelectasis,D001261,11,1
0.918896529,1,206,Fetal Distress,D005316,11,1
0.919885716,1,207,"Hearing Loss, Central",D006313,11,1
0.919885716,1,207,Hyperexplexia,D000071017,11,1
0.921828221,1,209,Generalized Epilepsy with Febrile Seizures Plus,C565808,11,1
0.921828221,1,209,Long Qt Syndrome 2,C563614,11,1
0.921828221,1,209,Myotonia,D009222,11,1
0.922781826,1,210,Currarino triad,C536221,11,1
0.923723855,1,211,Chondrodysplasia Punctata,D002806,11,1
0.923723855,1,211,"Breast Cancer, Familial Male",C566178,11,1
0.918896529,1,206,Myokymia,D020385,10,1
0.919885716,1,207,Anterior segment mesenchymal dysgenesis,C537775,10,1
0.919885716,1,207,"Anemia, Pernicious",D000752,10,1
0.919885716,1,207,Thecoma,D013798,10,1
0.920862899,1,208,Nicolaides Baraitser syndrome,C536116,10,1
0.920862899,1,208,OVERLAP CONNECTIVE TISSUE DISEASE,C536030,10,1
0.920862899,1,208,"Nephrogenic Diabetes Insipidus, Type I",D018500,10,1
0.920862899,1,208,Subaortic stenosis,D001020,10,1
0.921828221,1,209,"ARTHROGRYPOSIS, DISTAL, TYPE 2B",C538400,10,1
0.921828221,1,209,Hypokalemic periodic paralysis,D020514,10,1
0.921828221,1,209,Episodic ataxia type 2 (disorder),C535506,10,1
0.921828221,1,209,"Electron Transport Chain Deficiencies, Mitochondrial",D028361,10,1
0.922781826,1,210,"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B",C536122,10,1
0.922781826,1,210,Electrocardiogram,D004562,10,1
0.922781826,1,210,"CATARACT, COPPOCK-LIKE",C565133,10,1
0.691929852,2,198,"Congenital dyserythropoietic anemia, type I",D000742,5,1
0.707559116,2,204,"EHLERS-DANLOS SYNDROME, PROGEROID FORM",C536201,5,1
0.707559116,2,204,Brachydactyly type C,C537093,5,1
0.710099065,2,205,Separation Anxiety Disorder,D001010,5,1
0.710099065,2,205,"Thanatophoric dysplasia, type 2",C536508,5,1
0.437110367,3,201,Chromosome 15q13.3 Microdeletion Syndrome,C567439,2,1
0.918896529,1,206,Wolman Disease,D015223,9,1
0.918896529,1,206,Vulvar Lichen Sclerosus,D007724,9,1
0.918896529,1,206,Onycholysis,D054039,9,1
0.918896529,1,206,Vestibular Diseases,D015837,9,1
0.918896529,1,206,Dextrocardia,D003914,9,1
0.918896529,1,206,"Hyperferritinemia, hereditary, with congenital cataracts",C538137,9,1
0.918896529,1,206,"Glycosuria, Renal",D006030,9,1
0.918896529,1,206,Obstruction of pelviureteric junction,C537373,9,1
0.918896529,1,206,Osteochondromatosis,D018216,9,1
0.918896529,1,206,Asperger Syndrome,D020817,9,1
0.919885716,1,207,Congenital Pain Insensitivity,D000699,9,1
0.919885716,1,207,"FAMILIAL ADENOMATOUS POLYPOSIS, ATTENUATED (disorder)",C538265,9,1
0.919885716,1,207,Congenital musculoskeletal anomalies,D009139,9,1
0.920862899,1,208,Pulmonary Veno-Occlusive Disease (disorder),D011668,9,1
0.920862899,1,208,Jaw Abnormalities,D007569,9,1
0.920862899,1,208,Ventricular Dysfunction,D018754,9,1
0.921828221,1,209,Amputation Stumps,D000672,9,1
0.921828221,1,209,"46, XX Testicular Disorders of Sex Development",D058531,9,1
0.921828221,1,209,Oculocutaneous albinism type 1,C537728,9,1
0.921828221,1,209,HYPERPARATHYROIDISM 3,C566450,9,1
0.440281626,3,202,"Craniometaphyseal dysplasia, autosomal recessive type",C536570,2,1
0.440281626,3,202,"Amelogenesis Imperfecta, Hypomaturation Type, with Snow-Capped Teeth",C564463,2,1
0.440281626,3,202,"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1C",C563362,2,1
0.440281626,3,202,Senter syndrome,C536168,2,1
0.440281626,3,202,Familial Multiple Lipomatosis,D000071070,2,1
0.91585546,1,203,"Renal Tubular Acidosis, Type II",D000141,8,1
0.91688155,1,204,"Ocular albinism, type I",C537863,8,1
0.91688155,1,204,Retinal Vasculitis,D031300,8,1
0.91789519,1,205,"Early Childhood Epilepsy, Myoclonic",D004831,8,1
0.91789519,1,205,"Cardiomyopathy, Familial Hypertrophic, 1 (disorder)",C566005,8,1
0.91789519,1,205,"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1",C567924,8,1
0.91789519,1,205,Papilledema,D010211,8,1
0.91789519,1,205,Amelogenesis imperfecta nephrocalcinosis,C538241,8,1
0.91789519,1,205,"Hemiplegic migraine, familial type 1",C536890,8,1
0.918896529,1,206,Congenital Hand Deformities,D006228,8,1
0.918896529,1,206,Congenital exomphalos,D006554,8,1
0.918896529,1,206,Drowsiness,D012894,8,1
0.918896529,1,206,Canavan Disease,D017825,8,1
0.918896529,1,206,Pallister-Hall syndrome,D054975,8,1
0.919885716,1,207,Congenital hypomyelinating neuropathy,C535301,8,1
0.919885716,1,207,Persistent Hyperplastic Primary Vitreous,D054514,8,1
0.920862899,1,208,"Dementia, familial Danish",C538209,8,1
0.920862899,1,208,"Urea Cycle Disorders, Inborn",D056806,8,1
0.920862899,1,208,Partial atrioventricular canal,C536112,8,1
0.920862899,1,208,Short Qt Syndrome,C580439,8,1
0.702423837,2,202,"Niemann-Pick Disease, Type A",D052536,4,1
0.702423837,2,202,Penile Diseases,D010409,4,1
0.70500073,2,203,"NIEMANN-PICK DISEASE, TYPE C2",C536119,4,1
0.707559116,2,204,Nonsyndromic Holoprosencephaly,C580335,4,1
0.707559116,2,204,Overactive Detrusor,D053201,4,1
0.707559116,2,204,"Hibernation, Myocardial",D017682,4,1
0.707559116,2,204,Chylothorax,D002916,4,1
0.707559116,2,204,Trisomy X syndrome,C535318,4,1
0.707559116,2,204,Neuraminidase 1 deficiency,C537366,4,1
0.707559116,2,204,Blood group deletion syndrome,C564038,4,1
0.91585546,1,203,Chromosome 1p36 Deletion Syndrome,C535362,7,1
0.91585546,1,203,Madelung Deformity,C562398,7,1
0.91688155,1,204,Mowat-Wilson syndrome,C536990,7,1
0.91688155,1,204,Microphthalmia associated with colobomatous cyst,C537463,7,1
0.91688155,1,204,Chloasma,D008548,7,1
0.91688155,1,204,"Gonadal Dysgenesis, 46,XX",D023961,7,1
0.91789519,1,205,Phencyclidine Abuse,D010623,7,1
0.91789519,1,205,Hyperhidrosis Palmaris Et Plantaris,C563185,7,1
0.91789519,1,205,"Hypomagnesemia 2, renal",C537152,7,1
0.91789519,1,205,"MIGRAINE, FAMILIAL HEMIPLEGIC, 2",C537246,7,1
0.91789519,1,205,Spinal Diseases,D013122,7,1
0.918896529,1,206,"Gangliosidoses, GM2",D020143,7,1
0.918896529,1,206,Single umbilical artery,D058529,7,1
0.918896529,1,206,"Rett Syndrome, Atypical",C567576,7,1
0.918896529,1,206,Rhabdomyoma,D012207,7,1
0.918896529,1,206,"MICROPHTHALMIA, ISOLATED 1",C565377,7,1
0.918896529,1,206,Exudative vitreoretinopathy 1,C536382,7,1
0.918896529,1,206,HUNTINGTON DISEASE-LIKE 2,C564708,7,1
0.918896529,1,206,Shprintzen-Goldberg syndrome,C537328,7,1
0.918896529,1,206,"Anticipation, Genetic",D020132,7,1
0.918896529,1,206,"Dementia, familial British",C538208,7,1
0.919885716,1,207,WAGR Syndrome,D017624,7,1
0.919885716,1,207,Prieto X-linked mental retardation syndrome,C535274,7,1
0.919885716,1,207,Townes syndrome,C536974,7,1
0.919885716,1,207,Amyloid Neuropathies,D017772,7,1
0.919885716,1,207,Penis agenesis,C536649,7,1
0.919885716,1,207,Juvenile Absence Epilepsy,D004832,7,1
0.919885716,1,207,"Charcot-Marie-Tooth disease, X-linked, 1",C535919,7,1
0.919885716,1,207,Cystadenofibroma,D062625,7,1
0.91585546,1,203,Noise-induced hearing loss,D006317,6,1
0.91585546,1,203,Early myoclonic encephalopathy,C562695,6,1
0.91585546,1,203,Cleft Soft Palate,C562950,6,1
0.91688155,1,204,PAROXYSMAL EXTREME PAIN DISORDER,C563475,6,1
0.91688155,1,204,Vitreous Hemorrhage,D014823,6,1
0.91688155,1,204,Neonatal disorder,D007232,6,1
0.91688155,1,204,Polysplenia Syndrome,D059446,6,1
0.91688155,1,204,Epileptic Syndromes,D000073376,6,1
0.91688155,1,204,Panniculitis,D015434,6,1
0.91688155,1,204,Glycogen Storage Disease Type IV,D006011,6,1
0.91688155,1,204,Parasomnia,D020447,6,1
0.91789519,1,205,Cap Myopathy,C579969,6,1
0.91789519,1,205,"Polyposis, Gastric",C562464,6,1
0.91789519,1,205,"ARTHROGRYPOSIS, DISTAL, TYPE 1",C535378,6,1
0.91789519,1,205,Jervell-Lange Nielsen Syndrome,D029593,6,1
0.91789519,1,205,Congenital absence of lung,C562992,6,1
0.91789519,1,205,Scott Syndrome,C563120,6,1
0.918896529,1,206,"BRACHYDACTYLY, TYPE A1 (disorder)",C537088,6,1
0.918896529,1,206,"Pituitary Hormone Deficiency, Combined, 1",C567803,6,1
0.918896529,1,206,SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR,C537342,6,1
0.918896529,1,206,Embolism and Thrombosis,D016769,6,1
0.918896529,1,206,Roberts-SC phocomelia syndrome,C535687,6,1
0.918896529,1,206,Scrapie,D012608,6,1
0.918896529,1,206,Bronchopneumonia,D001996,6,1
0.918896529,1,206,Sclerosteosis,C537525,6,1
0.918896529,1,206,Craniofacial Dysostosis,D003394,6,1
0.918896529,1,206,Euthyroid Goiter,C562732,6,1
0.918896529,1,206,"EPILEPSY, BENIGN NEONATAL, 2",C535466,6,1
0.918896529,1,206,"Chondromatosis, Synovial",D015838,6,1
0.918896529,1,206,Chiari-Frommel Syndrome,D002640,6,1
0.702423837,2,202,Extraversion (Psychology),D005120,3,1
0.70500073,2,203,Autoimmune Hypophysitis,D000069281,3,1
0.70500073,2,203,"Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease",C563789,3,1
0.70500073,2,203,Jet Lag Syndrome,D020179,3,1
0.70500073,2,203,"Hypercalcemia, Idiopathic, of Infancy",C562581,3,1
0.70500073,2,203,Labyrinthine disorder,D007759,3,1
0.70500073,2,203,"Asthma, Exercise-Induced",D001250,3,1
0.70500073,2,203,Water Intoxication,D014869,3,1
0.70500073,2,203,"Metachromatic Leukodystrophy, Adult-Type (disorder)",D007966,3,1
0.70500073,2,203,Farber Lipogranulomatosis,D055577,3,1
0.70500073,2,203,Synkinesis,D046608,3,1
0.70500073,2,203,GLYCOGEN STORAGE DISEASE Ic,C562805,3,1
0.70500073,2,203,"ICHTHYOSIFORM ERYTHRODERMA, CONGENITAL, NONBULLOUS, 1",C538603,3,1
0.914816767,1,202,Congenital pectus excavatum,D005660,5,1
0.914816767,1,202,"Charcot-Marie-Tooth disease, Type 1C",C537984,5,1
0.914816767,1,202,Medullary sponge kidney,D007691,5,1
0.914816767,1,202,Pigment dispersion syndrome (disorder),C563184,5,1
0.91585546,1,203,VACTERL Association,C536495,5,1
0.91585546,1,203,Ankylosis,D000844,5,1
0.91585546,1,203,Azotemia,D053099,5,1
0.91585546,1,203,Schizencephaly,D065707,5,1
0.91585546,1,203,LONG QT SYNDROME 3,C565840,5,1
0.91585546,1,203,Talipes Equinovalgus,D004863,5,1
0.91585546,1,203,Waardenburg Syndrome Type 1,D014849,5,1
0.91585546,1,203,Familial eosinophilia,C562722,5,1
0.91688155,1,204,Mucopolysaccharidosis VI,D009087,5,1
0.91688155,1,204,Preaxial Hallucal Polydactyly,C566632,5,1
0.91688155,1,204,Persistent Mullerian duct syndrome,C536665,5,1
0.91688155,1,204,"Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency",C562657,5,1
0.91688155,1,204,Left Ventricle Remodeling,D020257,5,1
0.91688155,1,204,"Developmental Delay, Epilepsy, and Neonatal Diabetes",C565253,5,1
0.91688155,1,204,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F",C535413,5,1
0.91688155,1,204,Multiple self-healing squamous epithelioma,C536150,5,1
0.91688155,1,204,"MYOPATHY, MYOSIN STORAGE (disorder)",C564253,5,1
0.91688155,1,204,Spinocerebellar Ataxia 10,C566874,5,1
0.91688155,1,204,Branchioma,D001935,5,1
0.91688155,1,204,Galactorrhea,D005687,5,1
0.91789519,1,205,Nonorganic Sleep Wake Cycle Disorders,D020178,5,1
0.91789519,1,205,"Corneal dystrophy, Fuchs' endothelial, 1",C535478,5,1
0.91789519,1,205,Hypoactive Sexual Desire Disorder,D020018,5,1
0.91789519,1,205,Oculocutaneous albinism type 2,C537730,5,1
0.91789519,1,205,Angiokeratoma,D000794,5,1
0.91789519,1,205,Eisenmenger Complex,D004541,5,1
0.91789519,1,205,Klippel-Feil Syndrome,D007714,5,1
0.91789519,1,205,"HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE III",C537147,5,1
0.91789519,1,205,Hereditary bundle branch system defect,C566873,5,1
0.91789519,1,205,Acrocallosal Syndrome,D055673,5,1
0.91789519,1,205,"Muscular dystrophy congenital, merosin negative",C537384,5,1
0.91789519,1,205,Ovarian Fibromata,C562391,5,1
0.91789519,1,205,Hemifacial microsomia,D006053,5,1
0.91789519,1,205,Digitotalar Dysmorphism,C565097,5,1
0.91789519,1,205,"Achondrogenesis, type IB (disorder)",C536016,5,1
0.91789519,1,205,Nance-Horan syndrome,C538336,5,1
0.91789519,1,205,Hydrolethalus syndrome,C536079,5,1
0.91789519,1,205,Meckel Diverticulum,D008467,5,1
0.91789519,1,205,Ovotesticular Disorders of Sex Development,D050090,5,1
0.91789519,1,205,Loeys-Dietz Aortic Aneurysm Syndrome,D055947,5,1
0.912700953,1,200,Cerebellar Ataxia and Hypogonadotropic Hypogonadism,C565870,4,1
0.913765316,1,201,Cleft Palate with Ankyloglossia,C564442,4,1
0.913765316,1,201,Hennekam lymphangiectasia lymphedema syndrome,C537255,4,1
0.914816767,1,202,"Reflex, Biceps, Absent",D012021,4,1
0.914816767,1,202,Tricho-dento-osseous syndrome (disorder),C536549,4,1
0.914816767,1,202,Gonadal Disorders,D006058,4,1
0.914816767,1,202,Atrial Flutter,D001282,4,1
0.914816767,1,202,Dysgnathia complex,C537996,4,1
0.914816767,1,202,"OSTEOPETROSIS, AUTOSOMAL RECESSIVE 3",C536058,4,1
0.914816767,1,202,Otocephaly,C562503,4,1
0.914816767,1,202,"Diaphragm, Complete Agenesis Of",C564189,4,1
0.914816767,1,202,"CEROID LIPOFUSCINOSIS, NEURONAL, 5",C575534,4,1
0.91585546,1,203,"Distal Hereditary Motor Neuropathy, Type II",C580044,4,1
0.91585546,1,203,"ANEURYSM, INTRACRANIAL BERRY, 1 (disorder)",C566284,4,1
0.91585546,1,203,Nerve compression syndrome,D009408,4,1
0.91585546,1,203,"Charcot-Marie-Tooth disease, Type 2B2",C537991,4,1
0.91585546,1,203,Stress-induced polymorphic ventricular tachycardia,C536334,4,1
0.91585546,1,203,"Charcot-Marie-Tooth disease, Type 2I",C535416,4,1
0.91585546,1,203,Stenosis of duodenum,C535720,4,1
0.91585546,1,203,Brugada ECG Pattern,D053840,4,1
0.91585546,1,203,"GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 2",C565810,4,1
0.91585546,1,203,Urination Disorders,D014555,4,1
0.91585546,1,203,"Indifference to Pain, Congenital, Autosomal Recessive",C565467,4,1
0.91585546,1,203,Neural hearing loss,D012181,4,1
0.91585546,1,203,Gangliosidoses,D005733,4,1
0.91585546,1,203,"Ventricular Fibrillation, Paroxysmal Familial, 1",C567851,4,1
0.91585546,1,203,Decreased Libido,D007989,4,1
0.91585546,1,203,"Advanced Sleep-Phase Syndrome, Familial",C565789,4,1
0.91585546,1,203,Knee Dislocation,D031221,4,1
0.91585546,1,203,Cardio-Renal Syndrome,D059347,4,1
0.91688155,1,204,"WAARDENBURG SYNDROME, TYPE IIA",C536464,4,1
0.91688155,1,204,SeSAME syndrome,C557674,4,1
0.91688155,1,204,Deficiency Diseases,D003677,4,1
0.91688155,1,204,Annular pancreas,C536376,4,1
0.91688155,1,204,Physiological Sexual Disorders,D012735,4,1
0.91688155,1,204,Overbite,D057887,4,1
0.91688155,1,204,Brown oculocutaneous albinism,C562662,4,1
0.91688155,1,204,"BRACHYDACTYLY, TYPE A2",C537089,4,1
0.91688155,1,204,Facial Myokymia,D005155,4,1
0.91688155,1,204,"Axenfeld-Rieger Syndrome, Type 1",C535679,4,1
0.91688155,1,204,Short QT Syndrome 1,C566506,4,1
0.91688155,1,204,Cervical rib,D057070,4,1
0.91688155,1,204,Hematemesis,D006396,4,1
0.91688155,1,204,Aortic Valve Disease 1,C563178,4,1
0.91688155,1,204,Hereditary Hyperexplexia,C538136,4,1
0.91688155,1,204,LAURIN-SANDROW SYNDROME,C535689,4,1
0.91688155,1,204,"DIABETES MELLITUS, PERMANENT NEONATAL, WITH NEUROLOGIC FEATURES",C563424,4,1
0.91688155,1,204,Congenital absence of tibia,C535563,4,1
0.91688155,1,204,"Charcot-Marie-Tooth disease, Type 4B1",C535420,4,1
0.91688155,1,204,Renal cysts and diabetes syndrome,C535520,4,1
0.91688155,1,204,AMYOTROPHIC LATERAL SCLEROSIS 8 (disorder),C563895,4,1
0.91688155,1,204,"ALBINISM, OCULOCUTANEOUS, TYPE III",C537189,4,1
0.91688155,1,204,"DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT",C566366,4,1
0.91688155,1,204,Osteopoikilosis (disorder),D010023,4,1
0.91688155,1,204,NOONAN-LIKE/MULTIPLE GIANT CELL LESION SYNDROME (disorder),C537846,4,1
0.91688155,1,204,"SYMPHALANGISM, PROXIMAL",C536223,4,1
0.91688155,1,204,"KLIPPEL-FEIL SYNDROME, AUTOSOMAL DOMINANT",C536887,4,1
0.437110367,3,201,Loose Anagen Hair Syndrome,D058247,1,1
0.437110367,3,201,Alopecia congenita keratosis palmoplantaris,C537050,1,1
0.437110367,3,201,Pseudofolliculitis barbae (disorder),C563016,1,1
0.437110367,3,201,"CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 3 (disorder)",C535303,1,1
0.437110367,3,201,"Deafness, Autosomal Dominant 3B",C567215,1,1
0.437110367,3,201,Basaran Yilmaz syndrome,C537660,1,1
0.437110367,3,201,"Amelogenesis Imperfecta, Hypomaturation Type, Iia2",C567279,1,1
0.437110367,3,201,Amelogenesis imperfecta pigmented hypomaturation type,C538242,1,1
0.437110367,3,201,Adenoameloblastoma,C538229,1,1
0.437110367,3,201,"PALMOPLANTAR KERATODERMA, EPIDERMOLYTIC, WITH KNUCKLE PADS (disorder)",C564171,1,1
0.437110367,3,201,"Amelogenesis Imperfecta, Hypomaturation Type, Iia1",C567146,1,1
0.437110367,3,201,Crisscross Heart,D003420,1,1
0.437110367,3,201,"Pregnancy, Tubal",D011274,1,1
0.437110367,3,201,"Oculodentodigital Dysplasia, Autosomal Recessive",C567605,1,1
0.437110367,3,201,Congenital Deficiency of Pulmonary Surfactant Protein B,C553654,1,1
0.437110367,3,201,"Surfactant Metabolism Dysfunction, Pulmonary, 3",C567046,1,1
0.437110367,3,201,"SYNDACTYLY, TYPE III",C538154,1,1
0.437110367,3,201,Keratoconus posticus circumscriptus,C536151,1,1
0.437110367,3,201,"Amelogenesis Imperfecta, Type IB",C562879,1,1
0.437110367,3,201,"Neuronal Ceroid Lipofuscinosis, Congenital",C566438,1,1
0.437110367,3,201,"Amelogenesis Imperfecta, Type Ic",C567147,1,1
0.437110367,3,201,"Arhinia, choanal atresia, and microphthalmia",C537429,1,1
0.437110367,3,201,"Deafness, Autosomal Recessive 1b",C567213,1,1
0.69982837,2,201,"Dysarthria, Flaccid",D004401,2,1
0.69982837,2,201,Mononeuropathies,D020422,2,1
0.69982837,2,201,Ochoa syndrome,C536480,2,1
0.702423837,2,202,"Vitamin D Hydroxylation-Deficient Rickets, Type 1B",C564005,2,1
0.702423837,2,202,Generalized Spasms,D013035,2,1
0.702423837,2,202,Dentigerous Cyst,D003803,2,1
0.702423837,2,202,"Lamellar ichthyosis, type 2",C537264,2,1
0.702423837,2,202,Vasovagal syncope,D019462,2,1
0.702423837,2,202,Keutel syndrome,C536167,2,1
0.702423837,2,202,Sneezing,D012912,2,1
0.702423837,2,202,Cold Hypersensitivity,C569627,2,1
0.702423837,2,202,Proopiomelanocortin Deficiency,C565726,2,1
0.702423837,2,202,Drug Overdose,D062787,2,1
0.702423837,2,202,"Fractures, Closed",D005596,2,1
0.702423837,2,202,"Waardenburg Syndrome, Type 4c",C567679,2,1
0.702423837,2,202,"Hypoparathyroidism, Autosomal Recessive",C564148,2,1
0.702423837,2,202,Combined Saposin Deficiency,C567125,2,1
0.702423837,2,202,"Hypercalcemia, Infantile, 1",C562999,2,1
0.702423837,2,202,"Vitamin D-Dependent Rickets, Type 2A",C562794,2,1
0.702423837,2,202,Combat Disorders,D003130,2,1
0.702423837,2,202,Hyperostosis-hyperphosphatemia syndrome,C538381,2,1
0.702423837,2,202,"Retinal Necrosis Syndrome, Acute",D015882,2,1
0.913765316,1,201,Congenital anosmia,C535983,3,1
0.913765316,1,201,"Reflex Epilepsy, Photosensitive",D020195,3,1
0.913765316,1,201,Hexosaminidase alpha-Subunit Deficiency (Variant B),D013661,3,1
0.913765316,1,201,Brody myopathy,C536607,3,1
0.914816767,1,202,Familial schizencephaly,C538514,3,1
0.914816767,1,202,"Heart Rupture, Traumatic",D006335,3,1
0.914816767,1,202,Brachyolmia,C537098,3,1
0.914816767,1,202,"CARDIAC CONDUCTION DEFECT, NONSPECIFIC (disorder)",C567557,3,1
0.914816767,1,202,Amyotrophic Lateral Sclerosis 9,C567499,3,1
0.914816767,1,202,"Generalized Epilepsy With Febrile Seizures Plus, Type 6",C567371,3,1
0.914816767,1,202,Dermatopathia pigmentosa reticularis,C535374,3,1
0.914816767,1,202,Interfrontal craniofaciosynostosis,C562951,3,1
0.914816767,1,202,Acquired Neuromyotonia,D020386,3,1
0.914816767,1,202,Ectopic thyroid tissue (disorder),D050033,3,1
0.914816767,1,202,"MENTAL RETARDATION, X-LINKED 93 (disorder)",C567066,3,1
0.914816767,1,202,Warfarin syndrome,C536683,3,1
0.914816767,1,202,"Osteogenesis imperfecta, Levin type",C536039,3,1
0.914816767,1,202,Gonadal Agenesis,D006059,3,1
0.914816767,1,202,Polyasplenia,C566862,3,1
0.914816767,1,202,Homocarnosinosis,C535328,3,1
0.914816767,1,202,Gamma aminobutyric acid transaminase deficiency,C535407,3,1
0.914816767,1,202,"EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 1",C000600608,3,1
0.914816767,1,202,"Charcot-Marie-Tooth disease, Type 2A",C537988,3,1
0.914816767,1,202,Bleeding Disorder Due To P2RY12 Defect,C565220,3,1
0.914816767,1,202,3C syndrome,C535313,3,1
0.914816767,1,202,Hereditary motor and sensory neuropathy with optic atrophy (disorder),C562851,3,1
0.914816767,1,202,"MIGRAINE, SPORADIC HEMIPLEGIC",C563405,3,1
0.914816767,1,202,Cantu syndrome,C535572,3,1
0.914816767,1,202,"Empyema, Subdural",D013354,3,1
0.914816767,1,202,"Heterotaxy, Visceroatrial, Autosomal Recessive",C566864,3,1
0.914816767,1,202,Lens Diseases,D007905,3,1
0.914816767,1,202,"Ocular albinism, type II",C562664,3,1
0.91585546,1,203,"DEAFNESS, DIGENIC, GJB2/GJB3 (disorder)",C567134,3,1
0.91585546,1,203,Panayiotopoulos Syndrome,D020190,3,1
0.91585546,1,203,"Nemaline Myopathy, Autosomal Dominant",D017696,3,1
0.91585546,1,203,Somnambulism,D013009,3,1
0.91585546,1,203,"SARCOIDOSIS, EARLY-ONSET",C563714,3,1
0.91585546,1,203,Rh Deficiency Syndrome,C562717,3,1
0.91585546,1,203,Metrorrhagia,D008796,3,1
0.91585546,1,203,Weyers acrofacial dysostosis,C536695,3,1
0.91585546,1,203,"Rh-Null, Regulator Type",C564833,3,1
0.91585546,1,203,"Duane Retraction Syndrome, Type 3",D004370,3,1
0.91585546,1,203,"Sella Turcica, Bridged",C566689,3,1
0.91585546,1,203,"Anemia, Neonatal",D000751,3,1
0.91585546,1,203,HYDROLETHALUS SYNDROME 1,C565504,3,1
0.91585546,1,203,Cyclothymic Disorder,D003527,3,1
0.91585546,1,203,Paroxysmal nocturnal dyspnea,D004418,3,1
0.91585546,1,203,Hallux Varus,D050488,3,1
0.91585546,1,203,"Microphthalmia, Syndromic 3",C565948,3,1
0.91585546,1,203,Episodic ataxia type 1,C563278,3,1
0.91585546,1,203,Posterior Vitreous Detachment,D020255,3,1
0.91585546,1,203,Congenital absence of both testes,C537770,3,1
0.91585546,1,203,OROFACIAL CLEFT 11,C567410,3,1
0.91585546,1,203,"Acrocallosal syndrome, Schinzel type",C538177,3,1
0.91585546,1,203,Hyperekplexia and Epilepsy,C564474,3,1
0.91585546,1,203,Siderius X-linked mental retardation syndrome,C537333,3,1
0.91585546,1,203,Scapuloperoneal myopathy,C536624,3,1
0.91585546,1,203,Spermatocele,D013088,3,1
0.91585546,1,203,"Epileptic Encephalopathy, Early Infantile, 4",C567404,3,1
0.91585546,1,203,"Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive",D053360,3,1
0.91585546,1,203,OSLER-RENDU-WEBER SYNDROME 2,C537139,3,1
0.91585546,1,203,"2,8-Dihydroxyadenine Urolithiasis",C538228,3,1
0.91585546,1,203,Neuronal intranuclear inclusion disease,C537395,3,1
0.91585546,1,203,"FEBRILE CONVULSIONS, FAMILIAL, 8",C566975,3,1
0.91585546,1,203,5-Alpha Reductase Deficiency,C535830,3,1
0.91585546,1,203,"Papilloma, Intraductal",D018300,3,1
0.91585546,1,203,"Cystic Adenomatoid Malformation of Lung, Congenital",D015615,3,1
0.91585546,1,203,"Adenoma, Sweat Gland",D006607,3,1
0.91585546,1,203,"ALBINISM, OCULOCUTANEOUS, TYPE IB (disorder)",C537729,3,1
0.91585546,1,203,Greig cephalopolysyndactyly syndrome,C537300,3,1
0.91585546,1,203,"CEROID LIPOFUSCINOSIS, NEURONAL, 2",C566857,3,1
0.91585546,1,203,Deletion 11p13,C538295,3,1
0.91585546,1,203,Acromesomelic dysplasia Hunter-Thompson type,C535658,3,1
0.91585546,1,203,"Oculocutaneous Albinism, Type IV",C564696,3,1
0.91585546,1,203,"incomplete anencephaly, hemicrania",D000757,3,1
0.91585546,1,203,"EPILEPSY, FEMALE-RESTRICTED, WITH MENTAL RETARDATION (disorder)",C564715,3,1
0.91585546,1,203,Aberrant Crypt Foci,D058739,3,1
0.91585546,1,203,"Robinow syndrome, autosomal recessive",C535863,3,1
0.91585546,1,203,"Generalized Epilepsy With Febrile Seizures Plus, 7",C567827,3,1
0.91585546,1,203,"ALBINISM, OCULOCUTANEOUS, TYPE I, TEMPERATURE-SENSITIVE",C564645,3,1
0.91585546,1,203,Branchiootorenal Syndrome 2,D019280,3,1
0.91585546,1,203,Cleft Palate-Lateral Synechia Syndrome,C563047,3,1
0.91585546,1,203,"GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 3",C565811,3,1
0.91585546,1,203,Juvenile osteoporosis,C537700,3,1
0.91585546,1,203,Bladder Exstrophy and Epispadias Complex,C564009,3,1
0.91585546,1,203,Dissociative disorder,D004213,3,1
0.91585546,1,203,"Fibromatosis, Abdominal",D018221,3,1
0.91585546,1,203,NGLY1 deficiency,C000626124,3,1
0.91585546,1,203,LONG QT SYNDROME 9 (disorder),C567515,3,1
0.91585546,1,203,Desbuquois syndrome,C535943,3,1
0.91585546,1,203,Leri pleonosteosis,C537118,3,1
0.91585546,1,203,"Tay-Sachs Disease, AB Variant",D049290,3,1
0.91162352,1,199,Branchial Clefts-Congenital disorder,C562384,2,1
0.912700953,1,200,"PITUITARY HORMONE DEFICIENCY, COMBINED, 4",C567492,2,1
0.912700953,1,200,Keratosis palmoplantaris papulosa,C536161,2,1
0.913765316,1,201,"Chromosome 12, trisomy 12q",C538300,2,1
0.913765316,1,201,"MACULAR DYSTROPHY, ATYPICAL VITELLIFORM",C537832,2,1
0.913765316,1,201,Zlotogora-Ogur syndrome,C536726,2,1
0.913765316,1,201,Craniocervical Injuries,D020196,2,1
0.913765316,1,201,Neurotic Disorders,D009497,2,1
0.913765316,1,201,Kaposiform Hemangioendothelioma,C537007,2,1
0.913765316,1,201,"CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C",C535423,2,1
0.913765316,1,201,"Synovitis, Acne, Pustulosis, Hyperostosis, and Osteitis Syndrome",D020083,2,1
0.913765316,1,201,Focal Tonic Seizures,D020938,2,1
0.913765316,1,201,"Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3",C567690,2,1
0.913765316,1,201,"CARDIOMYOPATHY, DILATED, 1P",C563690,2,1
0.913765316,1,201,"Lymphangiectasis, Intestinal",D008201,2,1
0.913765316,1,201,Fetal megacystis,C536139,2,1
0.913765316,1,201,Klippel Feil syndrome recessive type,C536888,2,1
0.913765316,1,201,"Spondylometaphyseal dysplasia, axial",C535795,2,1
0.913765316,1,201,"Fabry Disease, Cardiac Variant",C567062,2,1
0.913765316,1,201,PANCREATIC AND CEREBELLAR AGENESIS,C563796,2,1
0.913765316,1,201,Aicardi's syndrome,D058540,2,1
0.913765316,1,201,BRACHYDACTYLY-SYNDACTYLY SYNDROME,C565193,2,1
0.914816767,1,202,Congenital chloride diarrhea,C536210,2,1
0.914816767,1,202,"GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 1",C565809,2,1
0.914816767,1,202,"Follicle-stimulating hormone deficiency, isolated",C537070,2,1
0.914816767,1,202,Frasier Syndrome,D052159,2,1
0.914816767,1,202,SPINOCEREBELLAR ATAXIA 31 (disorder),C566146,2,1
0.914816767,1,202,Conjunctival Diseases,D003229,2,1
0.914816767,1,202,"SPINOCEREBELLAR ATAXIA, X-LINKED 1",C563134,2,1
0.914816767,1,202,Otofaciocervical Syndrome,C563481,2,1
0.914816767,1,202,Multiple Synostoses Syndrome 3,C567839,2,1
0.914816767,1,202,"Gait, Athetotic",D020233,2,1
0.914816767,1,202,Oculocutaneous albinism type 3,C537731,2,1
0.914816767,1,202,Omodysplasia type 1,C537746,2,1
0.914816767,1,202,Hyaluronidase Deficiency,C563209,2,1
0.914816767,1,202,BRANCHIOOTIC SYNDROME 1,C537104,2,1
0.914816767,1,202,"CARDIOMYOPATHY, FAMILIAL, WITH CONDUCTION DISTURBANCE",C563984,2,1
0.914816767,1,202,Asherman Syndrome,D006175,2,1
0.914816767,1,202,Glucose Metabolism Disorders,D044882,2,1
0.914816767,1,202,Lumbosacral agenesis,C537221,2,1
0.914816767,1,202,Camptocormia,C537968,2,1
0.914816767,1,202,HEREDITARY HEMORRHAGIC TELANGIECTASIA-RELATED PULMONARY ARTERIAL HYPERTENSION,C563358,2,1
0.914816767,1,202,"Double Outlet Right Ventricle, Subpulmonary VSD",D004310,2,1
0.914816767,1,202,SHORT QT SYNDROME 2 (disorder),C566505,2,1
0.914816767,1,202,"Heterotaxy, Visceral, 5, Autosomal",C538116,2,1
0.914816767,1,202,Dysplasia epiphysealis hemimelica,C537997,2,1
0.914816767,1,202,"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2",C564064,2,1
0.914816767,1,202,"Aphakia, congenital primary",C537786,2,1
0.914816767,1,202,Keratosis Palmaris et Plantaris Familiaris,D015776,2,1
0.914816767,1,202,"Chromosome 7, trisomy 7p",C537819,2,1
0.914816767,1,202,Fibular hypoplasia and complex brachydactyly,C537931,2,1
0.914816767,1,202,Chromosome 11p deletion syndrome,C541598,2,1
0.914816767,1,202,Pentalogy of Cantrell,D058502,2,1
0.914816767,1,202,"COPD, Severe Early-Onset",C566978,2,1
0.914816767,1,202,"Ectodermal Dysplasia 3, Anhidrotic",D053359,2,1
0.914816767,1,202,Kleefstra Syndrome,C563043,2,1
0.914816767,1,202,"Deafness, Autosomal Recessive 53",C566453,2,1
0.914816767,1,202,Short QT Syndrome 3,C566504,2,1
0.914816767,1,202,"POLYDACTYLY, PREAXIAL II (disorder)",C536311,2,1
0.914816767,1,202,CONE-ROD DYSTROPHY 3 (disorder),C565827,2,1
0.914816767,1,202,Schneckenbecken dysplasia,C536637,2,1
0.914816767,1,202,Melena,D008551,2,1
0.914816767,1,202,Lipoid congenital adrenal hyperplasia,C537027,2,1
0.914816767,1,202,"DEAFNESS, AUTOSOMAL RECESSIVE 48",C563720,2,1
0.914816767,1,202,Henipavirus Infections,D045464,2,1
0.914816767,1,202,"Epilepsy, Akinetic",D004829,2,1
0.914816767,1,202,"Febrile Convulsions, Familial, 3a",C567820,2,1
0.914816767,1,202,"ALBINISM, OCULAR, WITH LATE-ONSET SENSORINEURAL DEAFNESS (disorder)",C537043,2,1
0.914816767,1,202,Microcephaly autosomal dominant,C537323,2,1
0.914816767,1,202,Mixed sclerosing bone dystrophy,C537479,2,1
0.914816767,1,202,Long QT syndrome type 3,C537034,2,1
0.914816767,1,202,MULTIPLE SYNOSTOSES SYNDROME 2,C537380,2,1
0.914816767,1,202,"CEROID LIPOFUSCINOSIS, NEURONAL, 8",C537952,2,1
0.914816767,1,202,Left-Right Axis Malformations,C566610,2,1
0.914816767,1,202,"DIABETES MELLITUS, TRANSIENT NEONATAL, 3 (disorder)",C566432,2,1
0.914816767,1,202,"Generalized Epilepsy With Febrile Seizures Plus, Type 4",C565227,2,1
0.914816767,1,202,Fara Chlupackova syndrome,C537074,2,1
0.914816767,1,202,Bidirectional tachycardia,C535438,2,1
0.914816767,1,202,Iris Diseases,D007499,2,1
0.914816767,1,202,Cardiovascular Infections,D053821,2,1
0.914816767,1,202,Uterine Rupture,D014597,2,1
0.914816767,1,202,Syndactyly Cenani Lenz type,C538150,2,1
0.914816767,1,202,Oculodigitoesophagoduodenal syndrome,C537734,2,1
0.914816767,1,202,Vestibulodynia,D056650,2,1
0.914816767,1,202,"Episodic Ataxia, Type 7",C567459,2,1
0.914816767,1,202,"Hypersomnolence, Idiopathic",D020177,2,1
0.914816767,1,202,Prickle1-Related Progressive Myoclonus Epilepsy with Ataxia,C580388,2,1
0.914816767,1,202,"Cleft Lip, Congenital Healed",C563468,2,1
0.914816767,1,202,"Chondrodysplasia, Grebe type",C537915,2,1
0.914816767,1,202,"Pancreatic Agenesis, Congenital",C564908,2,1
0.914816767,1,202,"MESOMELIC DYSPLASIA, KANTAPUTRA TYPE",C535547,2,1
0.914816767,1,202,"Cholestasis-edema syndrome, Norwegian type",C535330,2,1
0.914816767,1,202,Salcedo syndrome,C537228,2,1
0.914816767,1,202,Port-wine stain with oculocutaneous melanosis,C537894,2,1
0.914816767,1,202,Spermatic Cord Torsion,D013086,2,1
0.914816767,1,202,Dmd-Associated Dilated Cardiomyopathy,C580047,2,1
0.914816767,1,202,Chylous Ascites,D002915,2,1
0.914816767,1,202,Familial idiopathic hypercalciuria,C562790,2,1
0.914816767,1,202,Spinocerebellar ataxia 13,C537195,2,1
0.914816767,1,202,"BRACHYDACTYLY, TYPE B1",C566196,2,1
0.914816767,1,202,beta-Mannosidosis,D044905,2,1
0.914816767,1,202,Paraquat lung,C537171,2,1
0.914816767,1,202,Multiple Personality Disorder,D009105,2,1
0.914816767,1,202,Transient Myeloproliferative Disorder of Down Syndrome,C566024,2,1
0.914816767,1,202,Facial Dysmorphism with Multiple Malformations,C565579,2,1
0.914816767,1,202,"Syndactyly, Type IV",C566092,2,1
0.914816767,1,202,Prolonged Electroretinal Response Suppression,C564243,2,1
0.914816767,1,202,"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5",C567018,2,1
0.69982837,2,201,Segmental Autonomic Dysfunction,D001342,1,1
0.69982837,2,201,Chromosome 5p13 Duplication Syndrome,C567717,1,1
0.69982837,2,201,"Hypophosphatasia, Perinatal Lethal",C567107,1,1
0.69982837,2,201,"Muscular Dystrophy, Congenital, Megaconial Type",C566527,1,1
0.69982837,2,201,"COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 8",C567685,1,1
0.69982837,2,201,Proximal Myopathy with Focal Depletion of Mitochondria,C563453,1,1
0.69982837,2,201,Osteoid osteoma,D010017,1,1
0.69982837,2,201,Fuhrmann syndrome,C538189,1,1
0.69982837,2,201,Autosomal dominant hypophosphatemic rickets,C562791,1,1
0.69982837,2,201,"[X]Spinal osteochondrosis, unspecified",D055035,1,1
0.69982837,2,201,"Niemann-Pick Disease, Nova Scotian Type",C564941,1,1
0.69982837,2,201,"Chromosome 10, monosomy 10p",C538288,1,1
0.69982837,2,201,Marshall-Smith syndrome,C536026,1,1
0.69982837,2,201,"Hirschsprung Disease, Cardiac Defects, and Autonomic Dysfunction",C563939,1,1
0.69982837,2,201,"Dentin, Secondary",D003809,1,1
0.69982837,2,201,Hypophosphatemic Rickets And Hyperparathyroidism,C567423,1,1
0.69982837,2,201,KALLMANN SYNDROME 4 (disorder),C565696,1,1
0.69982837,2,201,"ICHTHYOSIS, LAMELLAR, 5",C564699,1,1
0.69982837,2,201,"Dentin dyspalsia, Shields type 2",D003784,1,1
0.69982837,2,201,ABCD syndrome,C535334,1,1
0.69982837,2,201,"Niemann-Pick Disease, Intermediate, With Visceral Involvement And Rapid Progression",C567267,1,1
0.69982837,2,201,"Cleidocranial Dysplasia, Forme Fruste, With Brachydactyly",C566119,1,1
0.69982837,2,201,Caliciviridae Infections,D017250,1,1
0.69982837,2,201,Sense of smell altered,D000857,1,1
0.69982837,2,201,"Niemann-Pick Disease, Type F",C564366,1,1
0.69982837,2,201,"Pseudohypoaldosteronism, Type IIc",C564162,1,1
0.69982837,2,201,"Waardenburg Syndrome, Type 4b",C567680,1,1
0.69982837,2,201,Adult hypophosphatasia (disorder),C562647,1,1
0.69982837,2,201,"Chromosome 7, trisomy 7q",C537821,1,1
0.69982837,2,201,alpha-Fetoprotein Deficiency,C566300,1,1
0.69982837,2,201,Hypoparathyroidism - X-linked,C562782,1,1
0.69982837,2,201,Van der Woude syndrome 2,C536529,1,1
0.69982837,2,201,"Thyrotropin deficiency, isolated",C000610012,1,1
0.69982837,2,201,Jalili syndrome,C000596385,1,1
0.69982837,2,201,Stomatognathic System Abnormalities,D018640,1,1
0.69982837,2,201,Narcolepsy 1,C563534,1,1
0.69982837,2,201,Eye Manifestations,D005132,1,1
0.69982837,2,201,Al Awadi syndrome,C535612,1,1
0.69982837,2,201,Caudal Duplication Anomaly,C564315,1,1
0.69982837,2,201,Spondylosis,D055009,1,1
0.69982837,2,201,ODONTOHYPOPHOSPHATASIA (disorder),C564146,1,1
0.69982837,2,201,SPINOCEREBELLAR ATAXIA 18,C537197,1,1
0.69982837,2,201,"Deafness, Autosomal Dominant 48",C564322,1,1
0.69982837,2,201,Infantile Diarrhea,D003968,1,1
0.69982837,2,201,"Hypocalcemia, Autosomal Dominant, with Bartter Syndrome",C563374,1,1
0.69982837,2,201,Urethral obstruction sequence,C536477,1,1
0.69982837,2,201,"EPISODIC ATAXIA, TYPE 6 (disorder)",C567207,1,1
0.69982837,2,201,"CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY",C563974,1,1
0.69982837,2,201,"Hypercalciuria, childhood idiopathic",C536082,1,1
0.69982837,2,201,"Hypocalciuric Hypercalcemia, Acquired",C564151,1,1
0.69982837,2,201,Metaphyseal Dysplasia with Maxillary Hypoplasia and Brachydactyly,C563586,1,1
0.69982837,2,201,"Hypersomnia, Post-Traumatic",D020919,1,1
0.69982837,2,201,Ageusia,D000370,1,1
0.69982837,2,201,Cerebral Embolism,D020766,1,1
0.69982837,2,201,"Deafness, Autosomal Dominant 39, with Dentinogenesis Imperfecta 1",C565316,1,1
0.69982837,2,201,Childhood hypophosphatasia (disorder),C562440,1,1
0.69982837,2,201,Tissue Pain,D059226,1,1
0.69982837,2,201,Pilonidal Cyst,D010864,1,1
0.69982837,2,201,Icterus Gravis Neonatorum,D007567,1,1
0.69982837,2,201,Cone rod dystrophy amelogenesis imperfecta,C535976,1,1
0.69982837,2,201,Leukotriene C4 Synthase Deficiency,C565439,1,1
0.69982837,2,201,"T-cell immunodeficiency, congenital alopecia and nail dystrophy",C536781,1,1
0.69982837,2,201,Amaurosis hypertrichosis,C536604,1,1
0.69982837,2,201,"NIEMANN-PICK DISEASE, INTERMEDIATE, PROTRACTED NEUROVISCERAL (disorder)",C567268,1,1
0.913765316,1,201,Decerebrate State,D003655,1,1
0.913765316,1,201,Landau-Kleffner Syndrome,D018887,1,1
0.913765316,1,201,Yemenite deaf-blind hypopigmentation syndrome,C536771,1,1
0.913765316,1,201,"Diarrhea 4, Malabsorptive, Congenital",C563673,1,1
0.913765316,1,201,"TOOTH AGENESIS, SELECTIVE, 4 (disorder)",C563634,1,1
0.913765316,1,201,Foster-Kennedy Syndrome,D009901,1,1
0.913765316,1,201,HOLOPROSENCEPHALY 5,C566464,1,1
0.913765316,1,201,Lenz Majewski hyperostotic dwarfism,C537115,1,1
0.913765316,1,201,Myokymia 1,C567174,1,1
0.913765316,1,201,"OSTEOPETROSIS, AUTOSOMAL DOMINANT 1",C536056,1,1
0.913765316,1,201,Normokalemic Periodic Paralysis,D010245,1,1
0.913765316,1,201,Brugada Syndrome 8,C567732,1,1
0.913765316,1,201,"Hexosaminidase A Deficiency, Adult Type",C564783,1,1
0.913765316,1,201,"Benign Neonatal Epilepsy, Nonfamilial",D020936,1,1
0.913765316,1,201,"LISSENCEPHALY SYNDROME, NORMAN-ROBERTS TYPE",C537848,1,1
0.913765316,1,201,"GAUCHER DISEASE, ATYPICAL, DUE TO SAPOSIN C DEFICIENCY",C566435,1,1
0.913765316,1,201,Hyperkalemic Periodic Paralysis Type 2,D020513,1,1
0.913765316,1,201,"BEST VITELLIFORM MACULAR DYSTROPHY, MULTIFOCAL (disorder)",C567187,1,1
0.913765316,1,201,"Pituitary Hormone Deficiency, Combined, 3",C536710,1,1
0.913765316,1,201,"Cutis Laxa With Severe Pulmonary, Gastrointestinal, And Urinary Abnormalities",C567716,1,1
0.913765316,1,201,Laurence-Moon Syndrome,D007849,1,1
0.913765316,1,201,"Ceroid Lipofuscinosis, Neuronal, 7",C563989,1,1
0.913765316,1,201,"Visceral Neuropathy, Familial, Autosomal Dominant",C566502,1,1
0.913765316,1,201,Spinal Stenosis,D013130,1,1
0.913765316,1,201,4-hydroxyphenylacetic aciduria,C535315,1,1
0.913765316,1,201,"Spherocytosis, Type 4",C567208,1,1
0.913765316,1,201,Takao VCF Syndrome,C566051,1,1
0.913765316,1,201,Renal Aminoacidurias,D000608,1,1
0.913765316,1,201,Bpes With Ovarian Failure,C566222,1,1
0.913765316,1,201,METHEMOGLOBINEMIA TYPE IV,C567102,1,1
0.913765316,1,201,"Night Blindness, Congenital Stationary, Autosomal Dominant 3",C566475,1,1
0.913765316,1,201,"Microtia, Hearing Impairment, And Cleft Palate",C567359,1,1
0.913765316,1,201,"Deafness, autosomal dominant nonsyndromic sensorineural 17",C538050,1,1
0.913765316,1,201,Transaldolase Deficiency,C563207,1,1
0.913765316,1,201,"COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 6",C566039,1,1
0.913765316,1,201,BESTROPHINOPATHY,C567518,1,1
0.913765316,1,201,DNA Repair-Deficiency,D049914,1,1
0.913765316,1,201,Diaphragmatic Hernia 3,C565710,1,1
0.913765316,1,201,"MICROPHTHALMIA, ISOLATED 2",C566446,1,1
0.913765316,1,201,Familial infantile myasthenia,C535759,1,1
0.913765316,1,201,"DEAFNESS, AUTOSOMAL RECESSIVE 35",C563908,1,1
0.913765316,1,201,"CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT 2 (disorder)",C567045,1,1
0.913765316,1,201,MACROTHROMBOCYTOPENIA AND PROGRESSIVE SENSORINEURAL DEAFNESS,C537831,1,1
0.913765316,1,201,Neurocutaneous melanosis,C537387,1,1
0.913765316,1,201,"Synostosis, Carpal, with Dysplastic Elbow Joints and Brachydactyly",C566090,1,1
0.913765316,1,201,Mandibular Retroposition,D063173,1,1
0.913765316,1,201,"RENAL TUBULAR ACIDOSIS, DISTAL, WITH HEMOLYTIC ANEMIA (disorder)",C566910,1,1
0.913765316,1,201,Retinal Nonattachment And Falciform Detachment,C566717,1,1
0.913765316,1,201,Psychogenic polydipsia,D059607,1,1
0.913765316,1,201,"MICROPHTHALMIA, SYNDROMIC 6 (disorder)",C566440,1,1
0.913765316,1,201,"Tay-Sachs Disease, Juvenile",C564782,1,1
0.913765316,1,201,Generalized Epilepsy and Paroxysmal Dyskinesia,C563719,1,1
0.913765316,1,201,"Schindler Disease, Type III",C536631,1,1
0.913765316,1,201,Furlong syndrome,C538192,1,1
0.913765316,1,201,"DEAFNESS, AUTOSOMAL DOMINANT 41 (disorder)",C564272,1,1
0.913765316,1,201,Premature Ovarian Failure 5,C566921,1,1
0.913765316,1,201,Myostatin-related muscle hypertrophy,C536106,1,1
0.913765316,1,201,Sulfoiduronate Sulfatase Deficiency,D016532,1,1
0.913765316,1,201,Cryptogenic Partial Complex Epilepsy,D017029,1,1
0.913765316,1,201,Fused Kidney,D000069337,1,1
0.913765316,1,201,"EPISODIC ATAXIA, TYPE 5",C566601,1,1
0.913765316,1,201,"Atrial Fibrillation, Familial, 3",C563817,1,1
0.913765316,1,201,"Aortic aneurysm, familial thoracic 3",C537783,1,1
0.913765316,1,201,Odontoonychodermal dysplasia,C537742,1,1
0.913765316,1,201,De La Chapelle Dysplasia,C535395,1,1
0.913765316,1,201,Phosphoribosylpyrophosphate synthetase deficiency,C537897,1,1
0.913765316,1,201,Winter Shortland Temple syndrome,C536735,1,1
0.913765316,1,201,"ACTH Deficiency, Isolated",C562707,1,1
0.913765316,1,201,"Sick Sinus Syndrome 2, Autosomal Dominant",C563513,1,1
0.913765316,1,201,"Parathyroid Adenomatosis, Familial Cystic",C564165,1,1
0.913765316,1,201,"Diffuse palmoplantar keratoderma, Bothnian type",C536173,1,1
0.913765316,1,201,Lowry Wood syndrome,C537038,1,1
0.913765316,1,201,"Ovalocytosis, Malaysian-Melanesian-Filipino Type",C566230,1,1
0.913765316,1,201,Ter Haar syndrome,C537274,1,1
0.913765316,1,201,Orofacial Cleft 9,C563675,1,1
0.913765316,1,201,"Tooth Agenesis, Selective, With Orofacial Cleft",C566994,1,1
0.913765316,1,201,HOLOPROSENCEPHALY 3,C564181,1,1
0.913765316,1,201,"Mental Retardation, X-Linked, Syndromic 14",C567063,1,1
0.913765316,1,201,"Leg, Absence Deformity of, with Congenital Cataract",C565442,1,1
0.913765316,1,201,"DEAFNESS, AUTOSOMAL RECESSIVE 44",C565716,1,1
0.913765316,1,201,Fucosidosis Type II,D005645,1,1
0.913765316,1,201,Spinocerebellar ataxia 22,C542540,1,1
0.913765316,1,201,Spondylometaphyseal Dysplasia with Cone-Rod Dystrophy,C563825,1,1
0.913765316,1,201,"Multicore Myopathy, Moderate, with Hand Involvement",C566147,1,1
0.913765316,1,201,"Deafness, Autosomal Dominant 2A",C567441,1,1
0.913765316,1,201,Lacrimal Apparatus Diseases,D007766,1,1
0.913765316,1,201,Brugada Syndrome 2,C567087,1,1
0.913765316,1,201,Pitt-Hopkins-Like Syndrome 1,C566482,1,1
0.913765316,1,201,Mullerian Aplasia and Hyperandrogenism,C567186,1,1
0.913765316,1,201,"Spondyloocular Syndrome, Autosomal Recessive",C565285,1,1
0.913765316,1,201,"Parathyroid Adenoma, Familial",C564166,1,1
0.913765316,1,201,Femoral Fractures,D005264,1,1
0.913765316,1,201,"Skeletal dysplasia, San Diego type",C536670,1,1
0.913765316,1,201,"POSTAXIAL POLYDACTYLY, TYPE B",C562429,1,1
0.913765316,1,201,Spondylocostal Dysostosis with Anal Atresia and Urogenital Anomalies,C564799,1,1
0.913765316,1,201,"DIABETES MELLITUS, INSULIN-DEPENDENT, 10",C566602,1,1
0.913765316,1,201,Temple-Baraitser Syndrome,C567516,1,1
0.913765316,1,201,"Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism",C565850,1,1
0.913765316,1,201,"Microphthalmia, Isolated 3",C567025,1,1
0.913765316,1,201,Hawkinsinuria,C535845,1,1
0.913765316,1,201,"Cardiomyopathy, Dilated, 1EE",C567683,1,1
0.913765316,1,201,Split-Hand-Foot Malformation With Sensorineural Hearing Loss,C565647,1,1
0.913765316,1,201,"Hypertelorism, Severe, With Midface Prominence, Myopia, Mental Retardation, And Bone Fragility",C566988,1,1
0.913765316,1,201,Goldberg-Shprintzen megacolon syndrome,C537279,1,1
0.913765316,1,201,"Gangliosidosis, Generalized GM1, Type 1 (disorder)",D016537,1,1
0.913765316,1,201,"NEUROMUSCULAR DISEASE, CONGENITAL, WITH UNIFORM TYPE 1 FIBER (disorder)",C567162,1,1
0.913765316,1,201,Platelet-Activating Factor Acetylhydrolase Deficiency,C566640,1,1
0.913765316,1,201,Pseudoarylsulfatase A Deficiency,C565403,1,1
0.913765316,1,201,"Chondrodysplasia, acromesomelic, with genital anomalies",C537913,1,1
0.913765316,1,201,"Renal tubular acidosis, distal, type 3",C537759,1,1
0.913765316,1,201,"Sandhoff Disease, Adult Type",C564825,1,1
0.913765316,1,201,Jaw Cysts,D007570,1,1
0.913765316,1,201,"DEAFNESS, AUTOSOMAL DOMINANT 23",C565357,1,1
0.913765316,1,201,"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 1",C565406,1,1
0.913765316,1,201,Atrial Septal Defect 5,C567561,1,1
0.913765316,1,201,Omodysplasia 2,C567664,1,1
0.913765316,1,201,Van Buchem disease type 2,C536527,1,1
0.913765316,1,201,Mannosidase Deficiency Diseases,D044904,1,1
0.913765316,1,201,"Normokalemic Periodic Paralysis, Potassium-Sensitive",C566809,1,1
0.913765316,1,201,"Renal Tubular Acidosis, Distal, Autosomal Recessive, with Late-Onset Sensorineural Hearing Loss",C566428,1,1
0.913765316,1,201,Birk-Barel Mental Retardation Dysmorphism Syndrome,C567357,1,1
0.913765316,1,201,CROUZON SYNDROME WITH ACANTHOSIS NIGRICANS (disorder),C567382,1,1
0.913765316,1,201,PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES (disorder),C563659,1,1
0.913765316,1,201,Atrial Septal Defect 3,C563540,1,1
0.913765316,1,201,"Keratitis, hereditary",C537022,1,1
0.913765316,1,201,"ALPHA/BETA T-CELL LYMPHOPENIA WITH GAMMA/DELTA T-CELL EXPANSION, SEVERE CYTOMEGALOVIRUS INFECTION, AND AUTOIMMUNITY",C563691,1,1
0.913765316,1,201,"Epilepsy, Benign Neonatal, 3",C564274,1,1
0.913765316,1,201,"Deafness, congenital onychodystrophy, recessive form",C538204,1,1
0.913765316,1,201,"HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE II (disorder)",C537146,1,1
0.913765316,1,201,"Nevi flammei, familial multiple",C535816,1,1
0.913765316,1,201,"Microphthalmia, Isolated, with Cataract 2",C565876,1,1
0.913765316,1,201,"Charcot-Marie-Tooth disease, Type 1E",C537986,1,1
0.913765316,1,201,SPLIT-HAND/FOOT MALFORMATION 6 (disorder),C567616,1,1
0.913765316,1,201,"Fasciitis, Plantar",D036981,1,1
0.913765316,1,201,"Ectopia Lentis, Spontaneous Filtering Blebs, and Craniofacial Dysmorphism",C563293,1,1
0.913765316,1,201,Familial acanthosis nigricans,C531598,1,1
0.913765316,1,201,"EXTERNAL AUDITORY CANAL, BILATERAL ATRESIA OF, WITH CONGENITAL VERTICAL TALUS",C566245,1,1
0.913765316,1,201,Long Qt Syndrome 6,C566333,1,1
0.913765316,1,201,"NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIA",C563561,1,1
0.913765316,1,201,"SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 5 (disorder)",C567119,1,1
0.913765316,1,201,"Diastrophic Dysplasia, Broad Bone-Platyspondylic Variant",C565626,1,1
0.913765316,1,201,CATSHL syndrome,C537975,1,1
0.913765316,1,201,Orofacial Cleft 12,C567548,1,1
0.913765316,1,201,"Spondyloepimetaphyseal Dysplasia, Pakistani Type",C567551,1,1
0.913765316,1,201,"Deafness, Autosomal Dominant 15",C566545,1,1
0.913765316,1,201,Ribbing disease,C537613,1,1
0.913765316,1,201,Metaphyseal Chondrodysplasia with Retinitis Pigmentosa,C565398,1,1
0.913765316,1,201,"Sulfatidosis, Juvenile, Austin Type",D052517,1,1
0.913765316,1,201,"Polydactyly, preaxial 4",C536333,1,1
0.913765316,1,201,O'Donnell Pappas syndrome,C537858,1,1
0.913765316,1,201,"MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 5 (disorder)",C566899,1,1
0.913765316,1,201,"Osteolysis, Hereditary, Of Carpal Bones With Or Without Nephropathy",C567171,1,1
0.913765316,1,201,"Charcot-Marie-Tooth Disease, Autosomal Dominant, Type 2k",C564325,1,1
0.913765316,1,201,"Gangliosidosis, Generalized GM1, Late-Infantile Type",C566893,1,1
0.913765316,1,201,Inflammatory Bowel Disease 12,C567388,1,1
0.913765316,1,201,"Gm2-Gangliosidosis, Variant B1",C567601,1,1
0.913765316,1,201,"Skin-Hair-Eye Pigmentation, Variation In, 11",C567374,1,1
0.913765316,1,201,"Micromelic dysplasia, congenital, with dislocation of radius",C537557,1,1
0.913765316,1,201,"Fibrous Dysplasia, Monostotic",D005358,1,1
0.913765316,1,201,"Patella aplasia, coxa vara, tarsal synostosis",C536307,1,1
0.913765316,1,201,Selective Mutism,D009155,1,1
0.913765316,1,201,"CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A (disorder)",C535419,1,1
0.913765316,1,201,Nivelon Nivelon Mabille syndrome,C536123,1,1
0.913765316,1,201,Diaphanospondylodysostosis,C564305,1,1
0.913765316,1,201,"Ventricular Fibrillation, Paroxysmal Familial, 2",C567841,1,1
0.913765316,1,201,"DIABETES MELLITUS, INSULIN-DEPENDENT, 20 (disorder)",C567286,1,1
0.913765316,1,201,Rapadilino syndrome,C535288,1,1
0.913765316,1,201,"Spastic Paraplegia 39, Autosomal Recessive",C567433,1,1
0.913765316,1,201,"DEAFNESS, AUTOSOMAL RECESSIVE 66",C565701,1,1
0.913765316,1,201,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7",C563753,1,1
0.913765316,1,201,Charcot-Marie-Tooth disease and deafness,C538078,1,1
0.913765316,1,201,"Masticatory Muscles, Hypertrophy of",C563600,1,1
0.913765316,1,201,"Spondyloepimetaphyseal Dysplasia, X-Linked",C564714,1,1
0.913765316,1,201,Hypoplastic enamel-onycholysis-hypohidrosis syndrome,C536736,1,1
0.913765316,1,201,Fibrinolytic Defect,C565017,1,1
0.913765316,1,201,Malignant hyperthermia susceptibility type 1,C535694,1,1
0.913765316,1,201,Brugada Syndrome 5,C567556,1,1
0.913765316,1,201,Long Qt Syndrome 10,C567514,1,1
0.913765316,1,201,"CARDIOMYOPATHY, DILATED, 1E",C563384,1,1
0.913765316,1,201,Wildervanck's syndrome,C535326,1,1
0.913765316,1,201,"Microcornea, Rod-Cone Dystrophy, Cataract, And Posterior Staphyloma",C536352,1,1
0.913765316,1,201,"Fibromatosis, Plantar",D000071380,1,1
0.913765316,1,201,Premature Ovarian Failure 6,C567351,1,1
0.913765316,1,201,"Darier Disease, Segmental",C565126,1,1
0.913765316,1,201,Brugada Syndrome 4,C567508,1,1
0.913765316,1,201,"Myopathy, Congenital, Compton-North",C567261,1,1
0.913765316,1,201,Lateral Medullary Syndrome,D014854,1,1
0.913765316,1,201,Pseudohypoparathyroidism Type 1C,C548076,1,1
0.913765316,1,201,JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME (disorder),C563412,1,1
0.913765316,1,201,"Optic Nerve Hypoplasia, Bilateral",C563492,1,1
0.913765316,1,201,Hematoma,D006406,1,1
0.913765316,1,201,"Hypokalemic Periodic Paralysis, Type 2",C567635,1,1
0.913765316,1,201,Posterior Leukoencephalopathy Syndrome,D054038,1,1
0.913765316,1,201,Genee-Wiedemann syndrome,C537680,1,1
0.913765316,1,201,Mycobacterium marinum Infection,C535526,1,1
0.913765316,1,201,"Tooth Agenesis, Selective, 3",C567036,1,1
0.913765316,1,201,"Chromosome 17, trisomy 17p",C538048,1,1
0.913765316,1,201,"Sex Reversal, Female, With Dysgenesis Of Kidneys, Adrenals, And Lungs",C567517,1,1
0.913765316,1,201,"Growth Retardation, Developmental Delay, Coarse Facies, And Early Death",C567856,1,1
0.913765316,1,201,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E (disorder)",C537994,1,1
0.913765316,1,201,"Orthostatic Hypotensive Disorder, Streeten Type",C564174,1,1
0.913765316,1,201,"Progressive Familial Heart Block, Type Ib",C567037,1,1
0.913765316,1,201,Brugada Syndrome 7,C567734,1,1
0.913765316,1,201,"Persistent Hyperplastic Primary Vitreous, Autosomal Recessive",C566966,1,1
0.913765316,1,201,Ovarian gynandroblastoma,C538459,1,1
0.913765316,1,201,ACHROMATOPSIA 4,C564206,1,1
0.913765316,1,201,"Rolandic Epilepsy, Mental Retardation, And Speech Dyspraxia, Autosomal Dominant",C563392,1,1
0.913765316,1,201,Oculootoradial syndrome,C535544,1,1
0.913765316,1,201,Autoimmune oophoritis,C538274,1,1
0.913765316,1,201,Brugada Syndrome 3,C567509,1,1
0.913765316,1,201,OROFACIAL CLEFT 5,C563843,1,1
0.913765316,1,201,"Spastic Paraplegia 42, Autosomal Dominant",C567262,1,1
0.913765316,1,201,OROFACIAL CLEFT 3,C563448,1,1
0.913765316,1,201,"Chromosome 2, trisomy 2p",C538318,1,1
0.913765316,1,201,"Visceral Myopathy, Familial",C562574,1,1
0.913765316,1,201,Spondylo-Megaepiphyseal-Metaphyseal Dysplasia,C567639,1,1
0.913765316,1,201,Cochleosaccular degeneration of the inner ear and progressive cataracts,C536432,1,1
0.913765316,1,201,Noonan Syndrome 6,C548084,1,1
0.913765316,1,201,"LOEYS-DIETZ SYNDROME, TYPE 1B",C567181,1,1
0.913765316,1,201,"Mental Retardation, X-Linked, Syndromic, Turner Type",C567476,1,1
0.913765316,1,201,"46,XY Gonadal Dysgenesis, Complete or Partial, DHH-Related",C565537,1,1
0.913765316,1,201,Kallmann Syndrome 6,C567199,1,1
0.913765316,1,201,Cloverleaf skull micromelia thoracic dysplasia,C536429,1,1
0.913765316,1,201,OROFACIAL CLEFT 2,C566419,1,1
0.913765316,1,201,Basal Cell Neoplasm,D018295,1,1
0.913765316,1,201,BRANCHIOOTIC SYNDROME 3 (disorder),C564248,1,1
0.913765316,1,201,"Chromosome 2, monosomy 2q24",C538316,1,1
0.913765316,1,201,"Aortic Aneurysm, Familial Thoracic 6",C567085,1,1
0.913765316,1,201,Frias syndrome,C535639,1,1
0.913765316,1,201,"EPIPHYSEAL DYSPLASIA, MULTIPLE, 4",C535504,1,1
0.913765316,1,201,"Exudative Vitreoretinopathy, Familial, X-Linked Recessive",C564428,1,1
0.913765316,1,201,"CEROID LIPOFUSCINOSIS, NEURONAL, 1",C564953,1,1
0.913765316,1,201,"Nephrolithiasis-Osteoporosis, Hypophosphatemic, 2",C567362,1,1
0.913765316,1,201,"Charcot-Marie-Tooth disease, Type 2H",C535415,1,1
0.913765316,1,201,"Microphthalmia, Cataracts, and Iris Abnormalities",C566448,1,1
0.913765316,1,201,Congenital Varicella Syndrome,D000073618,1,1
0.913765316,1,201,Body Fat Distribution,D050218,1,1
0.913765316,1,201,"Tay-Sachs Disease, Pseudo-AB Variant",C564786,1,1
0.913765316,1,201,"Charcot-Marie-Tooth Disease, Demyelinating, Type 1e",C566136,1,1
0.913765316,1,201,HOLOPROSENCEPHALY 4 (disorder),C564180,1,1
0.913765316,1,201,"Amelogenesis Imperfecta, Hypomaturation Type, Iia3",C567706,1,1
0.913765316,1,201,"Microphthalmia, Isolated, with Coloboma 3",C566447,1,1
0.913765316,1,201,Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies,C564621,1,1
0.913765316,1,201,Tabes Dorsalis,D013606,1,1
0.913765316,1,201,Worth disease,C536748,1,1
0.913765316,1,201,"Cardiomyopathy, Familial Hypertrophic, 14",C567684,1,1
0.913765316,1,201,"RENAL HYPOPLASIA, ISOLATED (disorder)",C537168,1,1
0.913765316,1,201,Metachromatic Leukodystrophy due to Saposin B Deficiency,C562609,1,1
0.913765316,1,201,"KRABBE DISEASE, ATYPICAL, DUE TO SAPOSIN A DEFICIENCY",C567097,1,1
0.913765316,1,201,9q22.3 Microdeletion,C579873,1,1
0.913765316,1,201,"Myoglobinuria, Acute Recurrent, Autosomal Recessive",C564832,1,1
0.913765316,1,201,PREMATURE OVARIAN FAILURE 3 (disorder),C563816,1,1
0.913765316,1,201,"Gm2-Gangliosidosis, Adult Chronic Type",C564784,1,1
0.913765316,1,201,HOLOPROSENCEPHALY 7,C563660,1,1
0.913765316,1,201,"CAP MYOPATHY, TPM3-RELATED (disorder)",C538348,1,1
0.913765316,1,201,Angel shaped phalangoepiphyseal dysplasia,C536361,1,1
0.913765316,1,201,Spondylodysplasia And Premature Pubarche,C567552,1,1
0.913765316,1,201,Premature Ovarian Failure 4,C564499,1,1
0.913765316,1,201,Blepharophimosis syndrome type 1,C536233,1,1
0.913765316,1,201,"Renal Tubular Acidosis, Distal, With Normal Red Cell Morphology",C566911,1,1
0.913765316,1,201,"Charcot-Marie-Tooth Disease, Recessive Intermediate A",C564256,1,1
0.913765316,1,201,Hereditary fructose intolerance syndrome,D005633,1,1
0.913765316,1,201,"Gangliosidosis, Generalized GM1, Type I, with Cardiac Involvement",C566895,1,1
0.913765316,1,201,"Sandhoff Disease, Juvenile Type",C564826,1,1
0.913765316,1,201,"Fleck Retina, Familial Benign",C565564,1,1
0.913765316,1,201,"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1F",C564242,1,1
0.913765316,1,201,"Hypercarotenemia And Vitamin A Deficiency, Autosomal Dominant",C567296,1,1
0.913765316,1,201,Borrone Di Rocco Crovato syndrome,C536577,1,1
0.913765316,1,201,"Acid cholesteryl ester hydrolase deficiency, type 2",C531854,1,1
0.913765316,1,201,King Denborough syndrome,C536883,1,1
0.913765316,1,201,"Mydriasis, Congenital",C563221,1,1
0.913765316,1,201,"Cardiomyopathy, Familial Hypertrophic, 11",C567419,1,1
0.913765316,1,201,Glycogen storage disease type Id,C562806,1,1
0.913765316,1,201,Oculoauricular Syndrome,C567416,1,1
0.913765316,1,201,EXUDATIVE VITREORETINOPATHY 4 (disorder),C566619,1,1
0.913765316,1,201,Myhre syndrome,C537620,1,1
0.913765316,1,201,Hypodontia Oligodontia with Orofacial Cleft,C566995,1,1
0.913765316,1,201,Plasminogen Activator Inhibitor-1 Deficiency,C567640,1,1
0.913765316,1,201,"Foveal Hypoplasia, Isolated",C565005,1,1
0.913765316,1,201,"SICK SINUS SYNDROME 1, AUTOSOMAL RECESSIVE",C563907,1,1
0.913765316,1,201,"Cardiac Conduction Defect, Nonprogressive",C566186,1,1
0.913765316,1,201,"Hepatic Adenomas, Familial",C564190,1,1
0.913765316,1,201,"RETINITIS PIGMENTOSA, CONCENTRIC (disorder)",C567712,1,1
0.913765316,1,201,Temtamy preaxial brachydactyly syndrome,C536958,1,1
0.913765316,1,201,"Blepharophimosis, Ptosis, and Epicanthus Inversus Type II",C562419,1,1
0.913765316,1,201,JERVELL AND LANGE-NIELSEN SYNDROME 2 (disorder),C567343,1,1
0.913765316,1,201,Perinatal death,D066087,1,1
0.913765316,1,201,Tufted angioma of skin,C536924,1,1
0.913765316,1,201,"Skin-Hair-Eye Pigmentation, Variation In, 4",C567300,1,1
0.913765316,1,201,Acrocapitofemoral Dysplasia,C564334,1,1
0.913765316,1,201,"WAARDENBURG SYNDROME, TYPE IID",C563839,1,1
0.913765316,1,201,Optic Nerve Hypoplasia and Abnormalities of the Central Nervous System,C565949,1,1
0.913765316,1,201,DEAFNESS-HYPOGONADISM SYNDROME,C564435,1,1
0.913765316,1,201,"CONE-ROD DYSTROPHY, X-LINKED, 3",C564507,1,1
0.913765316,1,201,Complement Factor D Deficiency,C565027,1,1
0.913765316,1,201,"Glutathione Peroxidase Deficiency, Hemolytic Anemia possibly due to",C564217,1,1
0.913765316,1,201,HOLOPROSENCEPHALY 2 (disorder),C563579,1,1
0.913765316,1,201,"Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation",C567038,1,1
0.913765316,1,201,Schinzel-Giedion syndrome,C536632,1,1
0.913765316,1,201,Blepharophimosis syndrome type 2,C536234,1,1
0.913765316,1,201,"Heart Block, Nonprogressive",C566185,1,1
0.913765316,1,201,Convergence Insufficiency,D015835,1,1
0.913765316,1,201,"Aortic Aneurysm, Familial Thoracic 2",C564627,1,1
0.913765316,1,201,Water Stress,D003681,1,1
0.913765316,1,201,"Neutropenia, Severe Congenital, Autosomal Dominant 2",C567748,1,1
0.913765316,1,201,"Sandhoff Disease, Infantile Type",C564827,1,1
0.913765316,1,201,Tietz syndrome,C536919,1,1
0.913765316,1,201,NEMALINE MYOPATHY 5,C538397,1,1
0.913765316,1,201,"Charcot-Marie-Tooth disease, Type 1D (disorder)",C537985,1,1
0.913765316,1,201,PROGRESSIVE ENCEPHALOMYELITIS WITH RIGIDITY,C566113,1,1
0.913765316,1,201,"Lesch-Nyhan Syndrome, Neurologic Variant",C564535,1,1
0.913765316,1,201,Agricultural Workers' Diseases,D000382,1,1
0.913765316,1,201,Retinitis Pigmentosa 20,C566718,1,1
0.913765316,1,201,Oligodontia-Colorectal Cancer Syndrome,C563898,1,1
0.913765316,1,201,"Atrial Fibrillation, Familial, 4",C566244,1,1
0.913765316,1,201,SCHOPF-SCHULZ-PASSARGE SYNDROME (disorder),C565607,1,1
0.913765316,1,201,RETINAL CONE DYSTROPHY 4,C566470,1,1
0.913765316,1,201,Palmoplantar Hyperkeratosis And True Hermaphroditism,C567165,1,1
0.913765316,1,201,"MICROPHTHALMIA, ISOLATED 4 (disorder)",C567757,1,1
0.913765316,1,201,"Darier Disease, Acral Hemorrhagic Type",C565125,1,1
0.913765316,1,201,"Tay-Sachs Disease, Variant B1",C564785,1,1
0.913765316,1,201,Orofacial Cleft 4,C564251,1,1
0.913765316,1,201,"LOEYS-DIETZ SYNDROME, TYPE 2A (disorder)",C567156,1,1
0.913765316,1,201,"46,Xy Gonadal Dysgenesis, Partial, With Minifascicular Neuropathy",C567773,1,1
0.913765316,1,201,Premature Ovarian Failure 2b,C564476,1,1
0.913765316,1,201,"Tooth Agenesis, Selective, X-Linked, 1",C567060,1,1
0.913765316,1,201,LONG QT SYNDROME 5,C566766,1,1
0.913765316,1,201,"Hypertension, Diastolic, Resistance to",C563897,1,1
0.913765316,1,201,"EPILEPSY, BENIGN NEONATAL, 1",C565164,1,1
0.913765316,1,201,Sick Building Syndrome,D018877,1,1
0.913765316,1,201,KBG syndrome,C537015,1,1
0.913765316,1,201,Nemaline Myopathy 7,C565198,1,1
0.913765316,1,201,"CATARACT, POSTERIOR POLAR, 1",C535339,1,1
0.913765316,1,201,"Epilepsy, Benign Neonatal, 1, And-Or Myokymia",C567743,1,1
0.913765316,1,201,Craniofacial deafness hand syndrome,C536453,1,1
0.913765316,1,201,Sudden unexpected nocturnal death syndrome,C531638,1,1
0.913765316,1,201,"Skin-Hair-Eye Pigmentation, Variation In, 10",C567376,1,1
0.913765316,1,201,"Atrial Fibrillation, Familial, 7",C567389,1,1
0.913765316,1,201,"Continuous Muscle Fiber Activity, Hereditary",C563545,1,1
0.913765316,1,201,Spinocerebellar ataxia 19,C537198,1,1
0.913765316,1,201,"Optic Nerve Aplasia, Bilateral",C563493,1,1
0.913765316,1,201,"Migraine, Familial Hemiplegic, 3",C566500,1,1
0.913765316,1,201,Chromosome 22q11.2 Microduplication Syndrome,C567224,1,1
0.913765316,1,201,Exudative Vitreoretinopathy 5,C567648,1,1
0.913765316,1,201,"Azoospermia, Nonobstructive",C564665,1,1
1,0,0,Sleep Initiation and Maintenance Disorders,D007319,4,1
1,0,0,Mitochondrial Encephalomyopathies,D017237,39,1
1,0,0,Bulbar palsy,D010244,25,1
1,0,0,Hypoaldosteronism,D006994,20,1
1,0,0,Lafora Disease,D020192,42,1
1,0,0,Glycogen Storage Disease Type V,D006012,13,1
1,0,0,Metaphyseal chondrodysplasia Schmid type,C537352,6,1
1,0,0,Smell Perception,D012903,40,1
1,0,0,Peroxisome biogenesis disorders,C536664,18,1
1,0,0,"Cerebral Palsy, Spastic Quadriplegic, 1",C567853,3,1
1,0,0,Microsatellite Instability,D053842,12,1
1,0,0,Hirsutism,D006628,63,1
1,0,0,Eye Color,D005127,11,1
1,0,0,Psychomotor Disorders,D011596,7,1
1,0,0,dowling-degos disease,C562924,13,1
1,0,0,Red Blood Cell Count measurement,D004906,100,1
1,0,0,"Myopathy, familial idiopathic inflammatory",C000598744,4,1
1,0,0,Seckel syndrome,C537533,34,1
1,0,0,Hand deformities,D006226,41,1
1,0,0,Dystonia Musculorum Deformans,D004422,18,1
1,0,0,Spondyloenchondrodysplasia,C535782,3,1
1,0,0,"Creatine deficiency, X-linked",C535598,6,1
1,0,0,Blepharophimosis,D016569,79,1
1,0,0,Developmental Coordination Disorder,D019957,9,1
1,0,0,Thromboxane synthetase deficiency,C562866,2,1
1,0,0,"USHER SYNDROME, TYPE IB (disorder)",C564755,7,1
1,0,0,Facies,D019066,8,1
1,0,0,Cohen syndrome,C536438,6,1
1,0,0,"Platelet Disorder, Familial, with Associated Myeloid Malignancy",C563324,4,1
1,0,2,"Anemia, Macrocytic",D000748,38,1
1,0,2,Linear atrophy,D057896,43,1
1,0,2,Apnea,D001049,67,1
1,0,2,MARDEN-WALKER SYNDROME,C535910,4,1
1,0,2,Cerebellar Hypoplasia,C562568,133,1
1,0,3,RETINITIS PIGMENTOSA 36,C566431,2,1
1,0,6,Biliary Tract Diseases,D001660,19,1
1,0,7,Drinking behavior processes,D004327,6,1
1,0,195,"Temporal epilepsy, familial",C536956,2,1
1,0,196,"CARDIOMYOPATHY, DILATED, 1C (disorder)",C563307,2,1
1,0,197,Spermatogenic Failure 7,C567832,2,1
1,0,198,"Leukodystrophy, Hypomyelinating, 2",C563855,2,1
1,0,198,"EPILEPSY, FAMILIAL ADULT MYOCLONIC, 1",C563399,2,1
1,0,198,Choledocholithiasis,D042883,3,1
1,0,198,"Deafness, Autosomal Dominant 4",C563460,2,1
1,0,199,Cat-Scratch Disease,D002372,2,1
1,0,200,RETINITIS PIGMENTOSA 9,C566716,7,1
1,0,200,Dyslalia,D013064,3,1
1,0,200,THYROID HORMONE PLASMA MEMBRANE TRANSPORT DEFECT,C536916,5,1
1,0,200,Hydroa Vacciniforme,D006837,4,1
1,0,200,"Infantile convulsions and paroxysmal choreoathetosis, familial (disorder)",C535522,3,1
1,0,200,"Thyroid Hormone Metabolism, Abnormal",C566454,2,1
1,0,200,Autosomal dominant compelling helio ophthalmic outburst syndrome,C535300,13,1
1,0,200,Diaphragmatic Eventration,D003965,7,1
1,0,200,SPINOCEREBELLAR ATAXIA 29,C537206,2,1
1,0,201,Glycogen Storage Disease IIIC,C566891,1,1
1,0,201,Illusions,D007088,1,1
1,0,201,Lymphedema-Distichiasis Syndrome with Renal Disease and Diabetes Mellitus,C567188,1,1
1,0,201,"Rett Syndrome, Zappella Variant",C567442,1,1
1,0,201,Pyruvate Dehydrogenase E1-Beta Deficiency,C566729,1,1
1,0,201,"Peroxisome Biogenesis Disorder, Complementation Group 3",C566633,1,1
1,0,201,Diamond-Blackfan Anemia 9,C567650,1,1
1,0,201,"Trichorhinophalangeal Syndrome, Type III",C566033,1,1
1,0,201,"Hyperthyroidism, Nonautoimmune",C563786,1,1
1,0,201,Saethre-Chotzen Syndrome with Eyelid Anomalies,C566325,1,1
1,0,201,Long Qt Syndrome 11,C567513,1,1
1,0,201,"Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis",C567770,1,1
1,0,201,"Deafness, Autosomal Recessive 23",C563705,1,1
1,0,201,"Polycystic Kidney Disease, Potter Type I, with Microbrachycephaly, Hypertelorism, and Brachymelia",C564881,1,1
1,0,201,OPTIC ATROPHY 7 (disorder),C567833,1,1
1,0,201,HYPOTRICHOSIS 6,C564312,1,1
1,0,201,"CILIARY DYSKINESIA, PRIMARY, 12",C567211,1,1
1,0,201,Long Qt Syndrome 4,C563428,1,1
1,0,201,Chromosome Deletion,D002872,1,1
1,0,201,Sacral Agenesis Syndrome,C566762,3,1
1,0,201,Fryns syndrome,C538070,1,1
1,0,201,Retinitis Pigmentosa 46,C567249,1,1
1,0,201,Lactate Dehydrogenase B Deficiency,C563641,1,1
1,0,201,Spinocerebellar Ataxia 12,C565790,1,1
1,0,201,"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2J",C563854,1,1
1,0,201,Sensorineural Deafness With Mild Renal Dysfunction,C567544,1,1
1,0,201,"Rhizomelic chondrodysplasia punctata, type 3",C537608,1,1
1,0,201,Sketetal dysplasia coarse facies mental retardation,C536671,1,1
1,0,201,Immunoglobulin a deficiency 2,C536291,1,1
1,0,201,"DYSTONIA 7, TORSION (disorder)",C566572,1,1
1,0,201,Aberrant subclavian artery,C535555,1,1
1,0,201,"Encephalocardiomyopathy, Mitochondrial, Neonatal, Due To Atp Synthase Deficiency",C567528,1,1
1,0,201,"CILIARY DYSKINESIA, PRIMARY, 10",C567287,1,1
1,0,201,Familial Glucocorticoid Deficiency Type 2,C564577,1,1
1,0,201,"Cataract, autosomal recessive congenital 2",C535337,1,1
1,0,201,"ATAXIA, SENSORY, AUTOSOMAL DOMINANT",C563818,1,1
1,0,201,SPINOCEREBELLAR ATAXIA 11,C565772,1,1
1,0,201,BARDET-BIEDL SYNDROME 12,C565921,1,1
1,0,201,"Infant, Extremely Low Birth Weight",D052577,1,1
1,0,201,Zimmerman Laband syndrome,C536725,2,1
1,0,201,Unilateral Multicystic Dysplastic Kidney,D021782,2,1
1,0,201,"Epiphyseal dysplasia, multiple, 2",C535502,1,1
1,0,201,"Epilepsy, Childhood Absence, Susceptibility To, 4",C567002,1,1
1,0,201,"Hepatitis, Chronic, Drug-Induced",D056487,1,1
1,0,201,"Molybdenum Cofactor Deficiency, Complementation Group A",C565372,1,1
1,0,201,Mitochondrial Phosphate Carrier Deficiency,C563665,1,1
1,0,201,De Barsy syndrome,C535990,1,1
1,0,201,"Hymen, Imperforate",C562397,2,1
1,0,201,"Larsen syndrome, recessive type",C537874,1,1
1,0,201,"FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3A, WITH OR WITHOUT EXTRAOCULAR INVOLVEMENT",C567572,1,1
1,0,201,Chronic Traumatic Encephalopathy,D000070627,1,1
1,0,201,N-Acetylneuraminic acid storage disease,C535525,1,1
1,0,201,Ichthyosis follicularis atrichia photophobia syndrome,C536085,1,1
1,0,201,"Brain Anomalies, Retardation, Ectodermal Dysplasia, Skeletal Malformations, Hirschsprung Disease, Ear-Eye Anomalies, Cleft Palate-Cryptorchidism, And Kidney Dysplasia-Hypoplasia",C564519,1,1
1,0,201,Beta-Ureidopropionase Deficiency,C563210,1,1
1,0,201,"Usher Syndrome, Type IF",C566586,1,1
1,0,201,Bartonella Infections,D001474,1,1
1,0,201,"Hyperandrogenism, Nonclassic Type, due to 21-Hydroxylase Deficiency",C565977,1,1
1,0,201,Ear Diseases,D004427,3,1
1,0,201,"Syndactyly, Type I",C566096,1,1
1,0,201,"DEAFNESS, AUTOSOMAL RECESSIVE 2",C564007,1,1
1,0,201,Mohr Syndrome,D009958,2,1
1,0,201,Deficiency of 3-oxoacid CoA-transferase,C537527,1,1
1,0,201,"Peroxisome Biogenesis Disorder, Complementation Group 4",C563301,1,1
1,0,201,Glycogen storage disease type X,C536176,1,1
1,0,201,"Tooth Agenesis, Selective, 5",C565757,1,1
1,0,201,Orofaciodigital syndrome type1,C537134,1,1
1,0,201,"Sertoli cell-only syndrome, Y-linked",C537587,1,1
1,0,201,CORNEA PLANA 1,C565158,1,1
1,0,201,Chromosome 2q32-Q33 Deletion Syndrome,C567350,1,1
1,0,201,Parastremmatic dwarfism,C537172,1,1
1,0,201,"Spastic paraplegia 11, autosomal recessive",C537483,1,1
1,0,201,Broad-Betalipoproteinemia,C566264,1,1
1,0,201,Food-Drug Interactions,D018565,1,1
1,0,201,"Retinal Degeneration, Autosomal Recessive, Clumped Pigment Type",C563527,1,1
1,0,201,Cerebrocostomandibular-Like Syndrome,C562538,2,1
1,0,201,Hyperprolinemia type 2,C538385,1,1
1,0,201,COWCHOCK SYNDROME,C536450,1,1
1,0,201,"Leukodystrophy, Hypomyelinating, 6",C567314,2,1
1,0,201,"Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 4",C566437,1,1
1,0,201,"Deafness, Autosomal Recessive 3",C563961,1,1
1,0,201,"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 13",C567714,1,1
1,0,201,Hereditary benign telangiectasia (disorder),C562908,1,1
1,0,201,"Macular Degeneration, Age-Related, 2",C562479,1,1
1,0,201,"Edema, Cardiac",D004489,3,1
1,0,201,"Decayed, Missing, and Filled Teeth",D004245,1,1
1,0,201,Chromosomal translocation,D014178,1,1
1,0,201,Opisthorchis felineus Infection,D009889,1,1
1,0,201,Estren-Dameshek Variant of Fanconi Pancytopenia,C565573,1,1
1,0,201,"Eunuchoidism, familial hypogonadotropic",C535764,1,1
1,0,201,"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 6",C567017,1,1
1,0,201,LEBER CONGENITAL AMAUROSIS 11,C564140,1,1
1,0,201,"Refsum Disease, Adult, 1",C567602,1,1
1,0,201,Phlebitis,D010689,1,1
1,0,201,"Chromosome 20, trisomy",C535372,1,1
1,0,201,"Spondyloepimetaphyseal dysplasia, Genevieve type",C535785,2,1
1,0,201,"Coloboma, cleft lip-palate and mental retardation syndrome",C535971,1,1
1,0,201,Glutamate formiminotransferase deficiency,C537425,1,1
1,0,201,Ribose 5-Phosphate Isomerase Deficiency,C563212,1,1
1,0,201,LEBER CONGENITAL AMAUROSIS 10 (disorder),C565720,1,1
1,0,201,Focal facial dermal dysplasia,C537068,2,1
1,0,201,JOUBERT SYNDROME 8 (disorder),C567358,1,1
1,0,201,Rectal Diseases,D012002,1,1
1,0,201,"CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ARCTIC VARIANT",C537944,1,1
1,0,201,Sparganosis,D013031,1,1
1,0,201,"CARDIOMYOPATHY, DILATED, 1I",C565752,1,1
1,0,201,"Scapuloperoneal Syndrome, Neurogenic, Kaeser Type",C566695,1,1
1,0,201,"Muscular dystrophy, tardive Emery-Dreifuss type, with contractures",C535734,1,1
1,0,201,"Myopathy, Reducing Body, X-Linked, Childhood-Onset",C567468,1,1
1,0,201,Anisakiasis,D017129,1,1
1,0,201,Retinal Cone Dystrophy 3A,C566483,1,1
1,0,201,"Liver Glycogenosis, X-Linked, Type II",C564421,1,1
1,0,201,"Atrial myxoma, familial",C538262,1,1
1,0,201,"CONE-ROD DYSTROPHY, X-LINKED, 1",C564438,1,1
1,0,201,Ghosal Hematodiaphyseal Dysplasia,C565551,1,1
1,0,201,"Myoglobinuria, Recurrent",C564018,1,1
1,0,201,Hydranencephaly with Renal Aplasia-Dysplasia,C565507,1,1
1,0,201,Reticular Dystrophy Of Retinal Pigment Epithelium,C566721,1,1
1,0,201,Marie Unna congenital hypotrichosis,C535912,1,1
1,0,201,Focal Segmental Glomerulosclerosis 5,C567687,1,1
1,0,201,"VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 2",C564393,1,1
1,0,201,"Apraxia, Ideomotor",D020240,1,1
1,0,201,"Macrocephaly, benign familial",C537717,1,1
1,0,201,Fryns-Aftimos Syndrome,C565258,1,1
1,0,201,ERYTHROKERATODERMIA VARIABILIS 3 (disorder),C563739,1,1
1,0,201,X-linked recessive nephrolithiasis with renal failure,C562901,1,1
1,0,201,Pyruvate Dehydrogenase E2 Deficiency,C565448,1,1
1,0,201,"Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to",C565545,1,1
1,0,201,"Mental Retardation, X-Linked, Syndromic 13",C566875,1,1
1,0,201,"INCLUSION BODY MYOPATHY 3, AUTOSOMAL DOMINANT",C565311,1,1
1,0,201,"Bile Acid Malabsorption, Primary",C567652,1,1
1,0,201,Diffuse Lewy Body Disease with Gaze Palsy,C565077,1,1
1,0,201,"Spastic Paraplegia-50, Autosomal Recessive",C567858,1,1
1,0,201,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2 (disorder)",C563757,1,1
1,0,201,"MACULAR DEGENERATION, AGE-RELATED, 3",C563838,1,1
1,0,201,Achromatopsia 3,C536129,1,1
1,0,201,Hemifacial Spasm,D019569,1,1
1,0,201,Labor Pain,D048949,1,1
1,0,201,"HYPERTRICHOSIS UNIVERSALIS CONGENITA, AMBRAS TYPE (disorder)",C536605,2,1
1,0,201,"Mental Retardation with Psychosis, Pyramidal Signs, and Macroorchidism",C564724,1,1
1,0,201,"ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS",C566878,1,1
1,0,201,Congenital disorder of glycosylation type 2A,C535752,1,1
1,0,201,Glycogen Storage Disease IXB,C563008,1,1
1,0,201,"Adenosine Triphosphate, Elevated, Of Erythrocytes",C566310,1,1
1,0,201,"Amyloidosis, Cerebral, with Spongiform Encephalopathy",C535800,1,1
1,0,201,Right Flank Pain,D021501,1,1
1,0,201,ELLIPTOCYTOSIS 3,C566678,1,1
1,0,201,"CILIARY DYSKINESIA, PRIMARY, 7 (disorder)",C567504,1,1
1,0,201,"Sialuria, French type",C537332,1,1
1,0,201,Pili annulati,C537187,1,1
1,0,201,"Hypertrichosis Terminalis, Generalized, with or without Gingival Hyperplasia",C565016,1,1
1,0,201,"Leber congenital amaurosis, type 4",C536999,1,1
1,0,201,Free sialic acid storage disease,C538523,1,1
1,0,201,"Ciliary Dyskinesia, Primary, 5",C563886,1,1
1,0,201,"Microcephaly, Primary Autosomal Recessive, 3",C565746,1,1
1,0,201,3-methylcrotonyl CoA carboxylase 2 deficiency,C535309,1,1
1,0,201,CONE-ROD DYSTROPHY 10,C564597,1,1
1,0,201,"Olivopontocerebellar hypoplasia, fetal-onset",C537745,1,1
1,0,201,"Gastroenteritis, Transmissible, of Swine",D005761,1,1
1,0,201,"FANCONI ANEMIA, COMPLEMENTATION GROUP D1",C563980,1,1
1,0,201,Skin Fragility-Woolly Hair Syndrome,C564359,1,1
1,0,201,"Cardiomyopathy, Dilated, 1J",C565337,1,1
1,0,201,"IRIDOGONIODYSGENESIS, TYPE 1 (disorder)",C535535,1,1
1,0,201,Phagocyte Bactericidal Dysfunction,D010585,1,1
1,0,201,"COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 5",C563456,1,1
1,0,201,Heme Oxygenase 1 Deficiency,C564200,1,1
1,0,201,"Natural Killer Cell Deficiency, Familial Isolated",C566492,1,1
1,0,201,"Tibia, Bowing of, with Pseudarthrosis and Pectus Excavatum",C563787,1,1
1,0,201,Methylenetetrahydrofolate reductase deficiency,C537357,1,1
1,0,201,"Lameness, Animal",D007794,1,1
1,0,201,Nemaline myopathy 4,C538351,1,1
1,0,201,Aging,D000375,3,1
1,0,201,Familial dermographism,C536612,1,1
1,0,201,Acne Keloid,D000153,1,1
1,0,201,Tetanilla,D013746,1,1
1,0,201,Athabaskan severe combined immunodeficiency,C536786,1,1
1,0,201,"Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism",C565705,1,1
1,0,201,Thyroid Dyshormonogenesis 4,C562770,1,1
1,0,201,Premature Ovarian Failure 2a,C564498,1,1
1,0,201,"Cardiomyopathy, Dilated, 1BB",C567877,1,1
1,0,201,"Ichthyosis, Congenital, with Trichothiodystrophy",C566643,1,1
1,0,201,Brachymesophalangy 2 and 5,C537097,1,1
1,0,201,SPINOCEREBELLAR ATAXIA 15,C564685,1,1
1,0,201,"Charcot-Marie-Tooth disease, Type 2J",C535417,1,1
1,0,201,Pyruvate Dehydrogenase E1 Alpha Deficiency,C564071,1,1
1,0,201,Ehlers-Danlos syndrome type 6,C536198,1,1
1,0,201,Diamond-Blackfan Anemia 8,C567253,1,1
1,0,201,Irritable heart,C531763,1,1
1,0,201,Groenouw corneal dystrophy type I (disorder),C537304,1,1
1,0,201,Neonatal Torulopsis glabrata Fungemia,C536972,1,1
1,0,201,"Mental Retardation, X-Linked, with Epilepsy",C564516,1,1
1,0,201,Dimethylglycine Dehydrogenase Deficiency,C565278,1,1
1,0,201,"Mental Retardation, Fra12a Type",C566980,1,1
1,0,201,PARIETAL FORAMINA 2,C566510,1,1
1,0,201,Retinitis Pigmentosa 26,C564249,1,1
1,0,201,Complement component 5 deficiency,C537005,1,1
1,0,201,Meige Syndrome,D008538,1,1
1,0,201,"Macrocytosis, Familial",C564004,1,1
1,0,201,"Fructose-1,6-Diphosphatase Deficiency",D015319,1,1
1,0,201,Gluthathione synthetase deficiency,C536835,1,1
1,0,201,"Ochronosis, hereditary",C537862,1,1
1,0,201,3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency,C567784,1,1
1,0,201,"Lower Extremity Deformities, Congenital",D038061,2,1
1,0,201,Pagetoid reticulosis,D056267,2,1
1,0,201,Spondyloepimetaphyseal Dysplasia With Joint Laxity,C562968,2,1
1,0,201,"Mental Retardation, X-Linked 79",C566876,1,1
1,0,201,"Deafness, Autosomal Recessive 37",C564331,1,1
1,0,201,CADASILM,D046589,2,1
1,0,201,Akinetic Mutism,D000405,1,1
1,0,201,"CHOROIDAL DYSTROPHY, CENTRAL AREOLAR 2",C567750,2,1
1,0,201,"Cardiomyopathy, Dilated, 1z",C567506,1,1
1,0,201,Triosephosphate Isomerase Deficiency,C566029,1,1
1,0,201,"MENTAL RETARDATION, X-LINKED, WITH SHORT STATURE, HYPOGONADISM, AND ABNORMAL GAIT",C567069,1,1
1,0,201,"DEAFNESS, AUTOSOMAL RECESSIVE 68",C563669,1,1
1,0,201,Brain Waves,D058256,3,1
1,0,201,RETINITIS PIGMENTOSA 12 (disorder),C563999,1,1
1,0,201,"COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 7 (disorder)",C565777,1,1
1,0,201,Breastfeeding Jaundice,C565501,1,1
1,0,201,LEBER CONGENITAL AMAUROSIS 9 (disorder),C536603,1,1
1,0,201,"Pseudohypoaldosteronism, Type IIb",C564161,1,1
1,0,201,"DEAFNESS, AUTOSOMAL RECESSIVE 6",C563418,1,1
1,0,201,RETINITIS PIGMENTOSA 19,C566637,1,1
1,0,201,Aspartylglucosamidase (AGA) deficiency,C538402,1,1
1,0,201,"Homocystinuria, Pyridoxine-Responsive",C565513,1,1
1,0,201,"POROKERATOSIS, DISSEMINATED SUPERFICIAL ACTINIC, 1",C536339,3,1
1,0,201,Coproporphyria,C535469,1,1
1,0,201,SPINOCEREBELLAR ATAXIA 26,C537203,1,1
1,0,201,Lethal Congenital Contracture Syndrome 2,C564369,1,1
1,0,201,Cone monochromatism,C536238,1,1
1,0,201,Meningocele,D008588,5,1
1,0,201,"USHER SYNDROME, TYPE IC",C564753,2,1
1,0,201,"Polycystic kidney disease, type 1",C536326,1,1
1,0,201,Kuru,D007729,1,1
1,0,201,"Retinitis Pigmentosa 7, Digenic",C567263,1,1
1,0,201,Brachial Plexus Neuritis,D020968,1,1
1,0,201,JOUBERT SYNDROME 3,C536295,1,1
1,0,201,Marie Unna Hereditary Hypotrichosis 1,C567718,1,1
1,0,201,Absence of tibia with polydactyly,C535564,1,1
1,0,201,"Syndactyly, Mesoaxial Synostotic, with Phalangeal Reduction",C563721,1,1
1,0,201,Sarcosinemia,C537236,1,1
1,0,201,"Peroxisome Biogenesis Disorder, Complementation Group 11",C566634,1,1
1,0,201,"Glycogen Storage Disease, Type IXA2",C567579,1,1
1,0,201,Long Qt Syndrome 12,C567842,1,1
1,0,201,Keratoderma with scleroatrophy of the extremities,C537526,1,1
1,0,201,Immune dysfunction with T-cell inactivation due to calcium entry defect 2,C557827,1,1
1,0,201,"Male Infertility with Large-Headed, Multiflagellar, Polyploid Spermatozoa",C562903,1,1
1,0,201,"Corneal Dystrophy, Lattice Type IIIA",C563923,1,1
1,0,201,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9",C566044,1,1
1,0,201,Retinitis Pigmentosa 31,C563685,1,1
1,0,201,"Leukodystrophy, Dysmyelinating, with Oligodontia",C564344,1,1
1,0,201,Megalocytic interstitial nephritis,C536144,1,1
1,0,201,"MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I",C537577,2,1
1,0,201,Schnyder crystalline corneal dystrophy,C535475,1,1
1,0,201,Vibratory angioedema,C536347,1,1
1,0,201,Thrombocytopenia Robin sequence,C536898,1,1
1,0,201,Absent corpus callosum cataract immunodeficiency,C535566,2,1
1,0,201,"FEBRILE CONVULSIONS, FAMILIAL, 4",C565788,1,1
1,0,201,Alzheimer Disease 7,C565251,1,1
1,0,201,Malignant hyperthermia susceptibility type 5,C535698,1,1
1,0,201,"Renal Tubular Transport, Inborn Errors",D015499,1,1
1,0,201,KERATOSIS PALMOPLANTARIS STRIATA II,C565102,1,1
1,0,201,Bosley-Salih-Alorainy Syndrome,C535397,1,1
1,0,201,"Methylmalonic Aciduria, mut(-) Type",C565390,1,1
1,0,201,Newfoundland Rod-Cone Dystrophy,C564391,1,1
1,0,201,"Hyperinsulinemic hypoglycemia, familial, 7",C538376,1,1
1,0,201,"Primary Lateral Sclerosis, Adult, 1",C566900,1,1
1,0,201,"HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 5",C567752,1,1
1,0,201,Thiopurine S methyltranferase deficiency,C536512,1,1
1,0,201,"Rhizomelic chondrodysplasia punctata, type 2",C537607,1,1
1,0,201,"Molybdenum Cofactor Deficiency, Complementation Group C",C565374,1,1
1,0,201,Melorheostosis with Osteopoikilosis,C563593,1,1
1,0,201,Osteopetrosis and infantile neuroaxonal dystrophy,C536055,1,1
1,0,201,Thrombocytopenia 4,C567438,1,1
1,0,201,"DEAFNESS, AUTOSOMAL RECESSIVE 15",C566611,1,1
1,0,201,"DEAFNESS, AUTOSOMAL RECESSIVE 63",C566951,1,1
1,0,201,"Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness",C562897,1,1
1,0,201,"KERATODERMA, PALMOPLANTAR, PUNCTATE TYPE II",C536338,1,1
1,0,201,Jejunal Atresia with Microcephaly and Ocular Anomalies,C565460,1,1
1,0,201,CEREBROOCULOFACIOSKELETAL SYNDROME 4,C565184,1,1
1,0,201,"Renal Failure, Progressive, with Hypertension",C562889,1,1
1,0,201,"Emery-Dreifuss Muscular Dystrophy 6, X-Linked",C567591,1,1
1,0,201,Uveoparotid Fever,D014608,1,1
1,0,201,Maxillofacial Abnormalities,D019767,1,1
1,0,201,"Colorectal Adenomatous Polyposis, Autosomal Recessive",C563924,1,1
1,0,201,Leigh necrotizing encephalopathy due to pyruvate carboxylase deficiency,C536255,1,1
1,0,201,"Peroxisome Biogenesis Disorder, Complementation Group E",C566569,1,1
1,0,201,N syndrome,C536108,1,1
1,0,201,"Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia",C564330,1,1
1,0,201,BARDET-BIEDL SYNDROME 6,C565738,1,1
1,0,201,JOUBERT SYNDROME 10 (disorder),C567582,1,1
1,0,201,"Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome",C537943,1,1
1,0,201,"Pregnancy Complications, Infectious",D011251,1,1
1,0,201,Chromosome Xp11.23-P11.22 Duplication Syndrome,C567585,1,1
1,0,201,Immunodeficiency due to Defect in MAPBP-Interacting Protein,C563663,1,1
1,0,201,Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency,C566449,1,1
1,0,201,"MICROCEPHALY, AMISH TYPE (disorder)",C538247,1,1
1,0,201,Fanconi like syndrome,C536855,1,1
1,0,201,"MECKEL SYNDROME, TYPE 4",C567003,1,1
1,0,201,"MENTAL RETARDATION, X-LINKED, WITH OR WITHOUT SEIZURES, ARX-RELATED (disorder)",C563150,1,1
1,0,201,Long chain acyl-CoA dehydrogenase deficiency,C535690,1,1
1,0,201,Salivary Gland Diseases,D012466,3,1
1,0,201,"FANCONI ANEMIA, COMPLEMENTATION GROUP B",C564497,1,1
1,0,201,"Preaxial deficiency, postaxial polydactyly and hypospadias",C538278,1,1
1,0,201,"Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate",C537405,1,1
1,0,201,Thumb in palm deformity,C562949,2,1
1,0,201,"OSTEOGENESIS IMPERFECTA, TYPE IX (disorder)",C564921,1,1
1,0,201,Insufficient Sleep Syndrome,D012892,1,1
1,0,201,BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 2,C567813,1,1
1,0,201,Spinal muscular atrophy 4,C538417,1,1
1,0,201,"Epilepsy, X-Linked, with Variable Learning Disabilities and Behavior Disorders",C564505,1,1
1,0,201,"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2 (disorder)",C564567,1,1
1,0,201,"Osteopetrosis, Autosomal Recessive 7",C567354,1,1
1,0,201,"Bone Fragility with Contractures, Arterial Rupture, and Deafness",C567320,1,1
1,0,201,"Pseudohyperkalemia, Familial, 2, due to Red Cell Leak",C563785,1,1
1,0,201,Familial myelofibrosis,C536848,1,1
1,0,201,JOUBERT SYNDROME 2,C536294,1,1
1,0,201,"46, XY Sex Reversal 5",C567766,1,1
1,0,201,"Charcot-Marie-Tooth Neuropathy, Dominant Intermediate B, with Neutropenia",C564704,1,1
1,0,201,"Purine-Pyrimidine Metabolism, Inborn Errors",D011686,1,1
1,0,201,Dependent Personality Disorder,D003859,1,1
1,0,201,Phosphoribosylpyrophosphate Synthetase Superactivity,C567064,1,1
1,0,201,"Welander distal myopathy, Swedish type",C536690,1,1
1,0,201,"MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE",C564494,1,1
1,0,201,"Pelizaeus-Merzbacher-like disease, autosomal recessive, 2",C536319,1,1
1,0,201,Myoclonic Cerebellar Dyssynergia,D002527,1,1
1,0,201,"Neuropathy, hereditary motor and sensory, Okinawa type",C535717,1,1
1,0,201,2-Methylbutyryl-CoA Dehydrogenase Deficiency,C566487,1,1
1,0,201,HAIM-MUNK SYNDROME,C537627,1,1
1,0,201,"Alcohol-Induced Disorders, Nervous System",D020268,1,1
1,0,201,Keratosis palmoplantaris striata 1,C536162,1,1
1,0,201,2-methyl-3-hydroxybutyric aciduria,C564560,1,1
1,0,201,Urethritis,D014526,1,1
1,0,201,Gait Apraxia,D020235,1,1
1,0,201,"Deafness, Autosomal Dominant 11",C563353,1,1
1,0,201,"Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Unusual Plaques",C564329,1,1
1,0,201,Deficiency of iodide peroxidase (disorder),C563206,1,1
1,0,201,"RETINITIS PIGMENTOSA, JUVENILE, LRAT-RELATED",C567636,1,1
1,0,201,Lentiginosis Profusa,C573023,1,1
1,0,201,Emery-Dreifuss Muscular Dystrophy 4,C567831,1,1
1,0,201,Striatonigral Degeneration,D020955,1,1
1,0,201,"Microphthalmia, syndromic 2",C537465,1,1
1,0,201,"FANCONI ANEMIA, COMPLEMENTATION GROUP I",C563802,1,1
1,0,201,Rotator cuff tear arthropathy,D000070656,1,1
1,0,201,"Mucolipidosis III Alpha Beta, Atypical",C567099,1,1
1,0,201,Trichorrhexis nodosa syndrome,C536556,1,1
1,0,201,Proud Syndrome,C563110,1,1
1,0,201,Hydranencephaly and Abnormal Genitalia,C564563,1,1
1,0,201,"Myopathy, congenital nonprogressive with Moebius and Robin sequences",C536102,1,1
1,0,201,Femur bifid with monodactylous ectrodactyly,C537917,1,1
1,0,201,Poland Syndrome,D011045,1,1
1,0,201,"Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2",C563750,1,1
1,0,201,Hyperlipemia with Familial Hypercholesterolemic Xanthomatosis,C566263,1,1
1,0,201,"Amyotrophic Lateral Sclerosis 6, Autosomal Recessive",C567699,1,1
1,0,201,Reye-Like Syndrome,D012202,1,1
1,0,201,"Molybdenum Cofactor Deficiency, Complementation Group B",C565373,1,1
1,0,201,"Deafness, autosomal dominant nonsyndromic sensorineural 22",C538197,1,1
1,0,201,Amish Infantile Epilepsy Syndrome,C563799,2,1
1,0,201,Duplication 15q11-q13 Syndrome,C557830,1,1
1,0,201,"Wolfram-Like Syndrome, Autosomal Dominant",C565631,1,1
1,0,201,NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2 (disorder),C565699,1,1
1,0,201,Brachial Plexus Neuropathies,D020516,1,1
1,0,201,"DIABETES MELLITUS, INSULIN-DEPENDENT, 5",C563958,1,1
1,0,201,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 8 (disorder)",C565188,1,1
1,0,201,Thyroid Dyshormonogenesis 6,C564608,1,1
1,0,201,"Charcot-Marie-Tooth disease, Type 2C",C537992,1,1
1,0,201,Senior-Loken Syndrome 3,C564637,1,1
1,0,201,Corpus callosum agenesis neuronopathy,C536446,2,1
1,0,201,Thrombocytopenia Paris-Trousseau type,C538617,1,1
1,0,201,"Hyperinsulinemic hypoglycemia, familial, 3",C538374,1,1
1,0,201,"Facial paresis, hereditary, congenital",C536386,1,1
1,0,201,Pseudo-Zellweger syndrome,C535818,1,1
1,0,201,Carney Complex Variant,C563845,1,1
1,0,201,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10",C563865,1,1
1,0,201,"Peroxisome Biogenesis Disorder, Complementation Group R",C566635,1,1
1,0,201,"Cholestasis, progressive familial intrahepatic 3",C535935,1,1
1,0,201,"COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 4",C563971,1,1
1,0,201,Kluver-Bucy Syndrome,D020232,1,1
1,0,201,"Hyperphenylalaninemia, BH4-Deficient, Due To Partial PTS Deficiency",C567493,1,1
1,0,201,Diamond-Blackfan Anemia 7,C567254,1,1
1,0,201,"Muscular Dystrophy, Limb-Girdle, Type 2G",C566599,1,1
1,0,201,Brugada Syndrome 6,C567735,1,1
1,0,201,"Diarrhea 3, Secretory Sodium, Congenital, Syndromic",C567490,1,1
1,0,201,Autosomal Recessive Cerebellar Ataxia Type 1,C579934,1,1
1,0,201,"Mental Retardation, X-Linked Nonsyndromic",C564490,1,1
1,0,201,"Mental Retardation, Autosomal Recessive 2",C564404,1,1
1,0,201,Abducens Nerve Diseases,C564661,1,1
1,0,201,Nemaline myopathy 6,C538398,1,1
1,0,201,"Smith-Lemli-Opitz Syndrome, Type I",D019082,1,1
1,0,201,De Quervain Disease,D053684,1,1
1,0,201,Histidinemia,C538320,2,1
1,0,201,Hemoglobin C Disease,D006445,1,1
1,0,201,Methylmalonate Semialdehyde Dehydrogenase Deficiency,C566402,1,1
1,0,201,Encephalomalacia,D004678,1,1
1,0,201,"Failure of Tooth Eruption, Primary",C565114,1,1
1,0,201,Townes-Brocks-Branchiootorenal-Like Syndrome,C566272,1,1
1,0,201,Neurocirculatory Asthenia,D009449,1,1
1,0,201,Episodic Kinesigenic Dyskinesia 2,C567026,1,1
1,0,201,LI-FRAUMENI SYNDROME 1,C538639,1,1
1,0,201,Floating-harbor syndrome,C537062,1,1
1,0,201,"Deafness, Sensorineural, And Male Infertility",C567010,1,1
1,0,201,"Stomatitis, Herpetic",D013283,1,1
1,0,201,"Hypothyroidism, Thyroidal, With Spiky Hair And Cleft Palate",C537901,2,1
1,0,201,Thiel-Behnke corneal dystrophy,C535942,1,1
1,0,201,Synpolydactyly 2,C564278,1,1
1,0,201,"Myopathy, Hyaline Body, Autosomal Recessive",C564970,1,1
1,0,201,RETINITIS PIGMENTOSA 27,C563526,1,1
1,0,201,"Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness",C567595,1,1
1,0,201,Myasthenic Syndrome due to Mutation in SCN4A,C565830,2,1
1,0,201,Tetraamelia multiple malformations,C536500,1,1
1,0,201,"Myopathy, Myofibrillar, Bag3-Related",C567843,1,1
1,0,201,Young Simpson syndrome,C536717,1,1
1,0,201,BARDET-BIEDL SYNDROME 7,C565916,1,1
1,0,201,"Ataxia, Spastic, 3, Autosomal Recessive",C566956,1,1
1,0,201,Mitchell-Riley Syndrome,C567570,1,1
1,0,201,Mandibulofacial Dysostosis with Mental Deficiency,C565420,1,1
1,0,201,Actin-Accumulation Myopathy,C579880,1,1
1,0,201,Reticular dysgenesis,C538361,1,1
1,0,201,"HYPOTRICHOSIS, CONGENITAL, WITH JUVENILE MACULAR DYSTROPHY",C537698,1,1
1,0,201,"MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 8, WITH EXOCRINE DYSFUNCTION",C565225,1,1
1,0,201,Faciogenital Dysplasia with Attention Deficit-Hyperactivity Disorder,C564427,1,1
1,0,201,Brunner Syndrome,C563156,1,1
1,0,201,CONE DYSTROPHY 4 (disorder),C567758,1,1
1,0,201,Inflammatory Bowel Disease 13,C567384,1,1
1,0,201,Caroli disease isolated,C531647,1,1
1,0,201,"Cardiomyopathy, Dilated, 1u",C566296,1,1
1,0,201,Bothnia Retinal Dystrophy,C564392,1,1
1,0,201,"Anemia, Diamond-Blackfan, 3",C536355,1,1
1,0,201,"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 12",C567019,1,1
1,0,201,"Nephrolithiasis-Osteoporosis, Hypophosphatemic, 1",C567363,1,1
1,0,201,"3-@METHYLGLUTACONIC ACIDURIA, TYPE V",C565706,2,1
1,0,201,Disseminated Fusariosis,D060585,1,1
1,0,201,Encephalitozoonosis,D016890,1,1
1,0,201,Dystransthyretinemic Euthyroidal Hyperthyroxinemia,C567719,1,1
1,0,201,"ATAXIA, SPASTIC, 2, AUTOSOMAL RECESSIVE (disorder)",C566969,1,1
1,0,201,Fatty Acid Hydroxylase-Associated Neurodegeneration,C580102,1,1
1,0,201,"Headache Disorders, Primary",D051270,1,1
1,0,201,Dihydropyrimidinase deficiency,C562815,1,1
1,0,201,Musician's Dystonia,C566973,2,1
1,0,201,Cerebrooculofacioskeletal Syndrome 2,C565185,1,1
1,0,201,Dermoid cyst of ovary,C562731,1,1
1,0,201,"GAUCHER DISEASE, PERINATAL LETHAL",C564306,1,1
1,0,201,Systemic Vasculitis,D056647,1,1
1,0,201,"Anemia, Sideroblastic, Autosomal Dominant",C567160,1,1
1,0,201,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 8",C563866,1,1
1,0,201,Deaf-Blind Syndromes,D054062,1,1
1,0,201,Ataxia Neuropathy Spectrum,C579922,1,1
1,0,201,"CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 5",C537129,1,1
1,0,201,Eiken Skeletal Dysplasia,C564010,1,1
1,0,201,Congenital absence of breast with absent nipple,C562989,1,1
1,0,201,"Deafness, Autosomal Recessive 21",C566353,1,1
1,0,201,"Cardiomyopathy, Familial Hypertrophic, 13",C567686,1,1
1,0,201,Tetra-amelia autosomal recessive,C536498,1,1
1,0,201,Succinate-Coa Ligase Deficiency,C580473,1,1
1,0,201,Arrest of spermatogenesis,C536875,2,1
1,0,201,"Spondyloepimetaphyseal Dysplasia, Shohat Type",C566523,1,1
1,0,201,Kahrizi Syndrome,C567196,1,1
1,0,201,Bardet-Biedl syndrome 2 (disorder),C537910,1,1
1,0,201,Cardiomyopathy dilated with Woolly hair and keratoderma,C535581,1,1
1,0,201,"CARDIOMYOPATHY, DILATED, 1X",C566907,1,1
1,0,201,"Dandy-Walker Syndrome, Familial",D003616,1,1
1,0,201,Sinoatrial Block,D012848,1,1
1,0,201,BARDET-BIEDL SYNDROME 11,C565920,3,1
1,0,201,Hyperphenylalaninemia with primapterinuria,C538382,1,1
1,0,201,"Properdin Deficiency, Type II",C564075,1,1
1,0,201,"Corneal dystrophy, epithelial basement membrane",C535477,1,1
1,0,201,"Cardiomyopathy, Dilated, 1y",C567507,1,1
1,0,201,Facial Hypertrichosis,C565029,4,1
1,0,201,"MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 7 (disorder)",C566466,1,1
1,0,201,RETINITIS PIGMENTOSA 33 (disorder),C563676,1,1
1,0,201,Metatropic dwarfism,C537356,1,1
1,0,201,"SPONDYLOEPIPHYSEAL DYSPLASIA, MAROTEAUX TYPE",C563218,1,1
1,0,201,"CILIARY DYSKINESIA, PRIMARY, 9",C567310,1,1
1,0,201,"Cardiomyopathy, Dilated, 1CC",C567733,1,1
1,0,201,"Migraine, Familial Basilar",C566540,1,1
1,0,201,"Deafness, Autosomal Dominant 9",C563335,1,1
1,0,201,"Folate Malabsorption, Hereditary",C562799,1,1
1,0,201,Gaucher-like disease,C537675,1,1
1,0,201,"Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to",C565557,1,1
1,0,201,RING DERMOID OF CORNEA,C535684,1,1
1,0,201,HUNTINGTON DISEASE-LIKE 1,C566398,1,1
1,0,201,Enterokinase Deficiency,C562649,1,1
1,0,201,Robinow Sorauf syndrome,C537183,1,1
1,0,201,"Chromosome 15q, trisomy",C538040,1,1
1,0,201,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 15",C567681,1,1
1,0,201,"Coloboma, Uveal, with Cleft Lip and Palate and Mental Retardation",C565173,1,1
1,0,201,"Retinitis Pigmentosa, Juvenile, Aipl1-Related",C565778,1,1
1,0,201,Chromosome 15q26-Qter Deletion Syndrome,C567232,1,1
1,0,201,RETINITIS PIGMENTOSA 42,C567854,1,1
1,0,201,Brachyolmia Type 3,C562963,1,1
1,0,201,"SPASTIC PARAPLEGIA 31, AUTOSOMAL DOMINANT",C565210,1,1
1,0,201,"SEIZURES, BENIGN FAMILIAL INFANTILE, 2",C565296,1,1
1,0,201,Orofaciodigital syndrome 5,C557819,1,1
1,0,201,"Deafness, Autosomal Recessive 22",C564633,1,1
1,0,201,"Spondyloepiphyseal Dysplasia, Kimberley Type",C564252,1,1
1,0,201,"Amyotrophic lateral sclerosis, type 6",C538251,1,1
1,0,201,"ATAXIA AND POLYNEUROPATHY, ADULT-ONSET",C564020,1,1
1,0,201,"Pericarditis, Constrictive",D010494,1,1
1,0,201,"Charcot-Marie-Tooth Disease, Axonal, Type 2a1",C566138,1,1
1,0,201,Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation,C567009,1,1
1,0,201,Thyroid Crisis,D013958,1,1
1,0,201,"Leukodystrophy, Dysmyelinating, And Spastic Paraparesis With Or Without Dystonia",C567311,1,1
1,0,201,Seborrhea-Like Dermatitis with Psoriasiform Elements,C565217,1,1
1,0,201,Intranuclear Rod Myopathy,C580202,1,1
1,0,201,"CARDIAC ARRHYTHMIA, ANKYRIN-B-RELATED",C566996,1,1
1,0,201,"Ectodermal dysplasia, ectrodactyly, and macular dystrophy",C536190,1,1
1,0,201,Schizophrenia Spectrum and Other Psychotic Disorders,D019967,1,1
1,0,201,"Xeroderma Pigmentosum, Type G-Cockayne Syndrome",C566879,1,1
1,0,201,Polyradiculoneuropathy,D011129,1,1
1,0,201,"Properdin Deficiency, Type III",C564076,1,1
1,0,201,Performance anxiety,D060805,1,1
1,0,201,"B-Cell Immunodeficiency, Distal Limb Anomalies, And Urogenital Malformations",C563745,1,1
1,0,201,Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria,C563693,1,1
1,0,201,"HYPOTHYROIDISM, CONGENITAL, DUE TO THYROID DYSGENESIS",C566852,1,1
1,0,201,MYOCLONUS AND ATAXIA,C535287,1,1
1,0,201,"Muscular Dystrophy, Limb-Girdle, Type 1D",C566370,1,1
1,0,201,BARDET-BIEDL SYNDROME 9,C565918,1,1
1,0,201,"USHER SYNDROME, TYPE IG",C564643,1,1
1,0,201,"PTOSIS, HEREDITARY CONGENITAL 1 (disorder)",C566737,1,1
1,0,201,Nakamura Osame syndrome,C538335,1,1
1,0,201,Temtamy syndrome,C536959,1,1
1,0,201,"Microcephaly, Primary Autosomal Recessive, 2",C565794,1,1
1,0,201,Floating-Betalipoproteinemia,C566265,1,1
1,0,201,"Ichthyosis, X-Linked, Complicated",C567443,1,1
1,0,201,Lipodystrophy with Congenital Cataracts and Neurodegeneration,C564669,1,1
1,0,201,"Chromosome 3, trisomy 3q",C536813,1,1
1,0,201,"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2M",C566912,1,1
1,0,201,"Gaucher Disease, Type IIIa",C565554,1,1
1,0,201,Fetal Malnutrition,D048070,1,1
1,0,201,"IRIDOGONIODYSGENESIS, TYPE 2",C535536,1,1
1,0,201,"Cardiac Valvular Defect, Developmental",C565882,1,1
1,0,201,"CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)",C567316,1,1
1,0,201,AICARDI-GOUTIERES SYNDROME 4,C563681,1,1
1,0,201,Genitopatellar Syndrome,C565255,1,1
1,0,201,"MENTAL RETARDATION, X-LINKED, SYNDROMIC 11",C537135,1,1
1,0,201,PONTOCEREBELLAR HYPOPLASIA TYPE 3 (disorder),C548072,1,1
1,0,201,"Neuropathy, Distal Hereditary Motor, Type VIIA",C563562,1,1
1,0,201,BARDET-BIEDL SYNDROME 10,C565919,1,1
1,0,201,Double cortex,C538475,1,1
1,0,201,"Skin-Hair-Eye Pigmentation, Variation In, 8",C567096,1,1
1,0,201,Cochlear Diseases,D015834,3,1
1,0,201,"Mthfr Deficiency, Thermolabile Type",C565512,1,1
1,0,201,"GRISCELLI SYNDROME, TYPE 1",C537301,1,1
1,0,201,Horner Syndrome,D006732,1,1
1,0,201,Acroosteolysis dominant type,C535663,1,1
1,0,201,"Refsum Disease, Adult, 2",C567603,1,1
1,0,201,Congenital absent nipple,C535565,1,1
1,0,201,"SPASTIC PARAPLEGIA 12, AUTOSOMAL DOMINANT (disorder)",C537484,1,1
1,0,201,"Hypomyelination, Global Cerebral",C567847,1,1
1,0,201,"Cholestasis, benign recurrent intrahepatic 2",C535934,1,1
1,0,201,Halitosis,D006209,1,1
1,0,201,"Hypospadias 2, X-Linked",C567462,1,1
1,0,201,Acrofacial dysostosis Rodriguez type,C538183,1,1
1,0,201,Cutaneous anthrax,C531621,1,1
1,0,201,Threatened abortion,D000033,1,1
1,0,201,Lemierre Syndrome,D057831,1,1
1,0,201,Urge Incontinence,D053202,3,1
1,0,201,Pyruvate dehydrogenase phosphatase deficiency,C536258,1,1
1,0,201,Cerebellar hypoplasia with endosteal sclerosis,C535353,1,1
1,0,201,"Deafness, Congenital Heart Defects, and Posterior Embryotoxon",C566604,1,1
1,0,201,Beriberi,D001602,1,1
1,0,201,"Cataract, Congenital Nuclear, Autosomal Recessive 3",C566923,1,1
1,0,201,Solitary Pulmonary Nodule,D003074,1,1
1,0,201,"Axenfeld-Rieger Anomaly with Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, and Skeletal Abnormalities",C566234,1,1
1,0,201,Anal Fistula,D012003,1,1
1,0,201,Heat Stress Disorders,D018882,1,1
1,0,201,Ppm-X Syndrome,C580387,1,1
1,0,201,Diamond-Blackfan Anemia 10,C567649,1,1
1,0,201,Karak Syndrome,C548029,1,1
1,0,201,Mediastinitis,D008480,1,1
1,0,201,Trichostrongyloidiasis,D014252,1,1
1,0,201,"Spondylometaphyseal dysplasia, Kozlowski type",C535797,1,1
1,0,201,Acheiropodia,C536014,1,1
1,0,201,BARDET-BIEDL SYNDROME 8,C565917,1,1
1,0,201,Endolymphatic Hydrops,D018159,1,1
1,0,201,"Spondyloepimetaphyseal Dysplasia, Aggrecan Type",C567558,1,1
1,0,201,Glycogen Storage Disease IIIA,C566889,1,1
1,0,201,Actinomycosis,D000196,1,1
1,0,201,Chromosome 3q29 Deletion Syndrome,C567184,1,1
1,0,201,"Glycogen Storage Disease 0, Liver",C565485,1,1
1,0,201,"Beta Thalassemia, Dominant Inclusion Body Type",C565834,1,1
1,0,201,"MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED (disorder)",C567708,1,1
1,0,201,"Peroxisome Biogenesis Disorder, Complementation Group 1",C566568,1,1
1,0,201,Retinitis Pigmentosa 14,C563992,1,1
1,0,201,Tukel syndrome,C536925,1,1
1,0,201,"SPASTIC PARAPLEGIA 18, AUTOSOMAL RECESSIVE (disorder)",C567628,1,1
1,0,201,"Acyl-CoA Dehydrogenase Family, Member 9, Deficiency of",C567006,1,1
1,0,201,"Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5",C567768,1,1
1,0,201,Toxic effect of heavy metal,D000075322,1,1
1,0,201,Curly hair-ankyloblepharon-nail dysplasia syndrome,C538074,1,1
1,0,201,Acromelic frontonasal dysplasia,C535657,1,1
1,0,201,"HYPERCHOLESTEROLEMIA, AUTOSOMAL DOMINANT, 3",C566337,1,1
1,0,201,"Deafness, Autosomal Dominant 20",C565754,1,1
1,0,201,Erythrocyte Amp Deaminase Deficiency,C567878,1,1
1,0,201,Lymphogranuloma Venereum,D008219,1,1
1,0,201,Chester-type porphyria,C536341,1,1
1,0,201,Protozoan Infections,D011528,1,1
1,0,201,"Charcot-Marie-Tooth Disease, Dominant Intermediate D",C564333,1,1
1,0,201,DYSTONIA 16 (disorder),C567430,3,1
1,0,201,"Bile acid synthesis defect, congenital, 2",C535443,1,1
1,0,201,Acquired Protein S Deficiency,C567077,1,1
1,0,201,"Auditory Neuropathy, Nonsyndromic Recessive",C563398,1,1
1,0,201,Alzheimer Disease 9,C563834,1,1
1,0,201,"Prostate Cancer, Hereditary, 12",C567510,1,1
1,0,201,RETINITIS PIGMENTOSA 30,C564310,1,1
1,0,201,REVESZ SYNDROME (disorder),C538371,1,1
1,0,201,Isobutyryl-CoA dehydrogenase deficiency,C535541,1,1
1,0,201,"NYSTAGMUS, INFANTILE PERIODIC ALTERNATING, X-LINKED (disorder)",C564478,1,1
1,0,201,LEBER CONGENITAL AMAUROSIS 5,C536602,1,1
1,0,201,Nephropathy with Pretibial Epidermolysis Bullosa and Deafness,C563798,1,1
1,0,201,Schizoid Personality Disorder,D012557,1,1
1,0,201,"Arrhythmogenic Right Ventricular Dysplasia, Familial, 8",C564400,1,1
1,0,201,FRIEDREICH ATAXIA WITH RETAINED REFLEXES,C564657,1,1
1,0,201,Polycystic Ovarian Disease due to 17-Ketosteroid Reductase Deficiency,C564868,1,1
1,0,201,Elejalde Disease,C536203,1,1
1,0,201,Toothache,D014098,1,1
1,0,201,OPTIC ATROPHY 1 AND DEAFNESS,C537124,1,1
1,0,201,"Myopathy, Early-Onset, with Fatal Cardiomyopathy",C567129,1,1
1,0,201,Shoulder Dislocation,D012783,1,1
1,0,201,"Whispering dysphonia, hereditary",C536698,1,1
1,0,201,"Pneumonia, Necrotizing",D000071067,2,1
1,0,201,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 2",C565865,1,1
1,0,201,"DEAFNESS, X-LINKED 4 (disorder)",C564723,1,1
1,0,201,Photosensitivity Disorders,D010787,1,1
1,0,201,HYPOMYELINATION AND CONGENITAL CATARACT,C567166,1,1
1,0,201,Preterm premature rupture of membranes (disorder),C563032,1,1
1,0,201,Orofaciodigital syndrome 3,C557817,2,1
1,0,201,"Spondylometaphyseal dysplasia, Sedaghatian type",C535798,1,1
1,0,201,"Porphyria, Acute Intermittent, Nonerythroid Variant",C566769,1,1
1,0,201,Linitis Plastica,D008039,1,1
1,0,201,"Aortic aneurysm, familial thoracic 4",C537784,1,1
1,0,201,Nemaline Myopathy 2,C538349,2,1
1,0,201,Massive Hepatic Necrosis,D047508,1,1
1,0,201,"CHOREOATHETOSIS/SPASTICITY, EPISODIC",C563401,1,1
1,0,201,Denial (Psychology),D003717,2,1
1,0,201,Familial hypertryptophanemia,C538393,1,1
1,0,201,"Cardiomyopathy, Dilated, 1FF",C567654,1,1
1,0,201,CODAS syndrome,C536434,1,1
1,0,201,Primary hyperoxaluria type 2,C536415,1,1
1,0,201,Acromegaloid facial appearance syndrome,C535655,1,1
1,0,201,"Mental Retardation, X-Linked, Syndromic, Christianson Type",C567484,1,1
1,0,201,Orofaciodigital syndrome 4,C537133,1,1
1,0,201,"Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4",C567023,1,1
1,0,201,"Cardiomyopathy, Dilated, 1AA",C567407,1,1
1,0,201,Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis,C545036,1,1
1,0,201,Gamma-cystathionase deficiency,C535408,1,1
1,0,201,"Cystinosis, benign, nonnephropathic",C535765,1,1
1,0,201,Jensen syndrome,C537568,1,1
1,0,201,Estren-Dameshek Variant of Fanconi Anemia,C565572,1,1
1,0,201,"Phobia, Specific",C562465,1,1
1,0,201,"Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis",C564050,1,1
1,0,201,"Arrhythmogenic Right Ventricular Dysplasia, Familial, 12",C566925,1,1
1,0,201,"Supranuclear Palsy, Progressive, 1, Atypical",C537240,1,1
1,0,201,Diaphyseal medullary stenosis with malignant fibrous histiocytoma,C536169,2,1
1,0,201,"Striatonigral Degeneration, Infantile, Mitochondrial",C564025,1,1
1,0,201,"Pyruvate Metabolism, Inborn Errors",D015323,1,1
1,0,201,"PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1 (disorder)",C566469,1,1
1,0,201,"Cerebrohepatorenal Syndrome, Variant Types",C565861,1,1
1,0,201,Diamond-Blackfan Anemia 4,C567281,1,1
1,0,201,Allan-Herndon-Dudley syndrome (AHDS),C537047,1,1
1,0,201,African Hemochromatosis,C579887,1,1
1,0,201,"Thyroid Adenoma, Hyperfunctioning",C566386,1,1
1,0,201,"DEAFNESS, AUTOSOMAL DOMINANT 6",C563421,1,1
1,0,201,"SPINAL MUSCULAR ATROPHY, LATE-ONSET, FINKEL TYPE",C566673,1,1
1,0,201,"LIMB-GIRDLE MUSCULAR DYSTROPHY, TYPE 1G (disorder)",C563794,1,1
1,0,201,"CARDIOMYOPATHY, DILATED, 1O",C563906,1,1
1,0,201,POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA,C536343,1,1
1,0,201,LEBER CONGENITAL AMAUROSIS 3 (disorder),C565814,1,1
1,0,201,AMYOTROPHIC LATERAL SCLEROSIS 5,C566576,1,1
1,0,201,"Bile acid synthesis defect, congenital, 1",C535442,1,1
1,0,201,"Deafness, Autosomal Recessive 16",C566339,1,1
1,0,201,"Deafness, Autosomal Recessive 67",C565207,1,1
1,0,201,Dyscalculia,D060705,1,1
1,0,201,Corticosteroid-Binding Globulin Deficiency,C565152,1,1
1,0,201,Nondystrophic myotonia,C536245,1,1
1,0,201,Chondromatosis,D018210,2,1
1,0,201,Emery-Dreifuss Muscular Dystrophy 3,C567633,1,1
1,0,201,"Peroxisome Biogenesis Disorder, Complementation Group K",C566624,1,1
1,0,201,"Peroxisome Biogenesis Disorder, Complementation Group 14",C563964,1,1
1,0,201,Sudden Infant Death with Dysgenesis of the Testes Syndrome,C563856,1,1
1,0,201,Trigger Finger Disorder,D052582,1,1
1,0,201,"Congenital Cataracts, Facial Dysmorphism, And Neuropathy",C565822,1,1
1,0,201,Microcephaly with Simplified Gyral Pattern,C566332,1,1
1,0,201,Cone-Rod Dystrophy 13,C567698,1,1
1,0,201,Urocanase deficiency,C536479,1,1
1,0,201,Complement Component 7 Deficiency,C566443,1,1
1,0,201,"Mental Retardation, Autosomal Dominant 3",C567241,4,1
1,0,201,Cystathionase Deficiency,C562680,1,1
1,0,201,"Gaucher Disease, Type Iiic",C565553,1,1
1,0,201,"Gaucher Disease, Norrbottnian Type",C565556,1,1
1,0,201,"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C",C567704,1,1
1,0,201,Cutis marmorata telangiectatica congenita,C536226,1,1
1,0,201,BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 3,C567772,1,1
1,0,201,"Cardiomyopathy, Dilated, 1w",C566954,1,1
1,0,201,"Thrombasthenia-Thrombocytopenia, Hereditary",C566060,1,1
1,0,201,Craniolenticulosutural Dysplasia,C564332,1,1
1,0,201,"alpha, alpha-Trehalase deficiency",C562603,1,1
1,0,201,Dysosteosclerosis,C562973,1,1
1,0,201,Pontocerebellar Hypoplasia Type 2B,C567325,1,1
1,0,201,"SPASTIC PARAPLEGIA 28, AUTOSOMAL RECESSIVE (disorder)",C563732,1,1
1,0,201,Cystic Kidney Disease with Ventriculomegaly,C565657,1,1
1,0,201,Becker Nevus Syndrome,C565735,1,1
1,0,201,Mental retardation Smith Fineman Myers type,C537445,1,1
1,0,201,"DERMATITIS HERPETIFORMIS, FAMILIAL",C538218,2,1
1,0,201,"Infant, Premature, Diseases",D007235,1,1
1,0,201,Borjeson-Forssman-Lehmann syndrome,C536575,1,1
1,0,201,"Mental Retardation, X-Linked, With Spasticity",C566877,1,1
1,0,201,Arakawa syndrome 2,C537426,1,1
1,0,201,Paratyphoid Fever,D010284,1,1
1,0,201,Deficiency of prolidase,D056732,1,1
1,0,201,Middle Lobe Syndrome,D008878,1,1
1,0,201,"MITRAL VALVE PROLAPSE, MYXOMATOUS 2",C564326,1,1
1,0,201,Herpes Zoster Oticus,D016697,1,1
1,0,201,Saccharopine dehydrogenase deficiency,C537218,1,1
1,0,201,Retinitis Pigmentosa 13,C564008,1,1
1,0,201,"MYOPATHY WITH EXERCISE INTOLERANCE, SWEDISH TYPE",C564972,1,1
1,0,201,"Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to",C564859,1,1
1,0,201,"OPTIC ATROPHY AND CATARACT, AUTOSOMAL DOMINANT",C537128,1,1
1,0,201,PONTOCEREBELLAR HYPOPLASIA TYPE 4 (disorder),C536716,1,1
1,0,201,"Charcot-Marie-Tooth Disease, Axonal, Type 2n",C567653,1,1
1,0,201,Young Syndrome,C536718,1,1
1,0,201,"46,XY Sex Reversal 4",C567887,1,1
1,0,201,"Syndactyly, type v",C538155,1,1
1,0,201,Nocturnal Myoclonus Syndrome,D020189,1,1
1,0,201,"Oral-facial-digital syndrome, type 2",C538585,1,1
1,0,201,Potter Type III Polycystic Kidney Disease,C566792,1,1
1,0,201,SPONGIFORM ENCEPHALOPATHY WITH NEUROPSYCHIATRIC FEATURES,C564678,1,1
1,0,201,microcephaly-digital anomalies syndrome,C567101,1,1
1,0,201,"Progressive Familial Heart Block, Type II",C564202,1,1
1,0,201,Achondrogenesis type 1A,C536015,1,1
1,0,201,"Beta-Aminoisobutyric Acid, Urinary Excretion of",C565904,1,1
1,0,201,Combined Malonic and Methylmalonic Aciduria,C580002,1,1
1,0,201,Peripheral Nerve Injuries,D059348,1,1
1,0,201,Hyperleucine-Isoleucinemia,C562674,1,1
1,0,201,"Bartter Syndrome, Type 3, with Hypocalciuria",C564578,1,1
1,0,201,"Ecthyma, Contagious",D004474,2,1
1,0,201,Elliptocytosis 1,C567520,1,1
1,0,201,"Deafness, Autosomal Dominant 10",C563354,1,1
1,0,201,Xeroderma Pigmentosum B-Cockayne Syndrome,C567061,1,1
1,0,201,Cerebrooculofacioskeletal Syndrome 3,C565035,1,1
1,0,201,SPINOCEREBELLAR ATAXIA 27,C537204,1,1
1,0,201,Acute fatty liver of pregnancy,C537957,1,1
1,0,201,"Deafness, Sensorineural, with Hypertrophic Cardiomyopathy",C565236,1,1
1,0,201,"Hearing Loss, Unilateral",D046088,1,1
1,0,201,"Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis",C537583,1,1
1,0,201,"Creutzfeldt-Jakob Disease, Heidenhain Variant",C566981,1,1
1,0,201,Prosopagnosia,D020238,1,1
1,0,201,Low T3 Syndrome,D005067,1,1
1,0,201,Thyroid Dyshormonogenesis 3,C562769,1,1
1,0,201,"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 3 (disorder)",C566170,1,1
1,0,201,Trichorhinophalangeal dysplasia type I,C536820,1,1
1,0,201,"Bile Acid Synthesis Defect, Congenital, 3",C566340,1,1
1,0,201,"Giant Axonal Neuropathy, Autosomal Dominant",C566444,1,1
1,0,201,"MECKEL SYNDROME, TYPE 2",C536131,1,1
1,0,201,Glomerulonephritis sparse hair telangiectases,C536825,1,1
1,0,201,Asphyxiating Thoracic Dystrophy 2,C566982,1,1
1,0,201,"Hereditary spastic paralysis, infantile onset ascending",C537217,1,1
1,0,201,"Macular Degeneration, Age-Related, 6",C563674,1,1
1,0,201,"RUSSELL-SILVER SYNDROME, X-LINKED",C562446,1,1
1,0,201,Alopecia-Mental Retardation Syndrome 1,C565965,1,1
1,0,201,Odontoma,D009810,1,1
1,0,201,Valinemia,C536524,1,1
1,0,201,Reis-Bucklers' corneal dystrophy,C535476,1,1
1,0,201,6-Phosphogluconolactonase Deficiency,C566803,1,1
1,0,201,"Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type",C565510,1,1
1,0,201,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 3",C537309,2,1
1,0,201,"Thrombophilia, Hereditary, Due To Protein S Deficiency, Autosomal Recessive",C567348,1,1
1,0,201,Cancer of Lip,D008048,1,1
1,0,201,Narcosis,D053608,1,1
1,0,201,MEACHAM SYNDROME (disorder),C538162,1,1
1,0,201,"DEAFNESS, X-LINKED 5 (disorder)",C564472,1,1
1,0,201,"Slowed Nerve Conduction Velocity, Autosomal Dominant",C564269,1,1
1,0,201,OPTIC ATROPHY 5 (disorder),C537126,1,1
1,0,201,"PARKINSON DISEASE 11, AUTOSOMAL DOMINANT",C564345,1,1
1,0,201,Primrose syndrome,C536420,1,1
1,0,201,ACROMELIC FRONTONASAL DYSOSTOSIS,C566345,1,1
1,0,201,"DEAFNESS, CHILDHOOD-ONSET NEUROSENSORY, AUTOSOMAL RECESSIVE 8",C563395,1,1
1,0,201,"CILIARY DYSKINESIA, PRIMARY, 13",C567713,1,1
1,0,201,"Deafness, Autosomal Dominant 44",C564399,1,1
1,0,201,Retinal Cone Dystrophy 3B,C563678,1,1
1,0,201,Radius Fractures,D011885,1,1
1,0,201,Pontocerebellar Hypoplasia Type 2A,C564738,1,1
1,0,201,Cytosolic acetoacetyl-CoA thiolase deficiency,C536005,1,1
1,0,201,Glycogen Storage Disease IIID,C566892,1,1
1,0,201,"Protoporphyria, Erythropoietic, X-Linked Dominant",C567464,1,1
1,0,201,Glycogen Storage Disease XII,C562718,1,1
1,0,201,"Deafness, Congenital, and Onychodystrophy, Autosomal Dominant",C567274,1,1
1,0,201,Lingual Thyroid,D046151,1,1
1,0,201,Aryl Hydrocarbon Hydroxylase Inducibility,C566250,1,1
1,0,201,"Arrhythmogenic Right Ventricular Dysplasia, Familial, 11",C566471,1,1
1,0,201,"Mycobacterium tuberculosis, susceptibility to infection by",C536092,1,1
1,0,201,"Progeria Syndrome, Childhood-Onset",C567661,1,1
1,0,201,Zunich neuroectodermal syndrome,C536729,1,1
1,0,201,Roifman syndrome,C535866,1,1
1,0,201,LEBER CONGENITAL AMAUROSIS 13,C567197,2,1
1,0,201,"Bile acid synthesis defect, congenital, 4",C535444,1,1
1,0,201,HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA SYNDROME,C564327,1,1
1,0,201,SMITH-MCCORT DYSPLASIA,C564589,3,1
1,0,201,"Digital Arthropathy-Brachydactyly, Familial",C564656,1,1
1,0,201,JOUBERT SYNDROME 5,C537688,1,1
1,0,201,"Deafness, Autosomal Recessive 79",C567651,1,1
1,0,201,Mercury Poisoning,D008630,1,1
1,0,201,Opsismodysplasia,C537122,1,1
1,0,201,Mental Processes,D008606,2,1
1,0,201,Erythrocyte Lactate Transporter Defect,C565449,1,1
1,0,201,"Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive",C564948,1,1
1,0,201,Stocco dos Santos syndrome,C537495,1,1
1,0,201,Kohlschutter Tonz syndrome,C537213,1,1
1,0,201,Methylmalonyl-CoA Epimerase Deficiency,C565386,1,1
1,0,201,"Hyperammonemia, type III",C536109,1,1
1,0,201,"PULMONARY VENOOCCLUSIVE DISEASE 2, AUTOSOMAL RECESSIVE",C535861,1,1
1,0,201,"SPASTIC PARAPLEGIA 30, AUTOSOMAL RECESSIVE (disorder)",C563677,1,1
1,0,201,"Lipodystrophy, Congenital Generalized, Type 3",C567282,1,1
1,0,201,Halothane Hepatitis,C562477,1,1
1,0,201,"MYOPATHY, X-LINKED, WITH POSTURAL MUSCLE ATROPHY (disorder)",C567480,1,1
1,0,201,"SCAPULOPERONEAL MYOPATHY, X-LINKED DOMINANT",C567481,2,1
1,0,201,Coronary Vessel Anomalies,D003330,1,1
1,0,201,Microphthalmia and mental deficiency,C537462,2,1
1,0,201,"BRACHYDACTYLY, TYPE D",C562420,1,1
1,0,201,Serpentine fibula polycystic kidney syndrome,C537586,1,1
1,0,201,SPLIT-HAND/FOOT MALFORMATION 3,C565437,1,1
1,0,201,"Mental retardation X-linked, South African type",C537450,1,1
1,0,201,"Epiphyses, Slipped",D004839,1,1
1,0,201,Phosphoserine Aminotransferase Deficiency,C567032,1,1
1,0,201,BARDET-BIEDL SYNDROME 13,C567140,1,1
1,0,201,Mucolipidosis 2,C538602,1,1
1,0,201,Dysbetalipoproteinemia due to Defect in Apolipoprotein E-d,C566261,1,1
1,0,201,"Adrenal Insufficiency, Congenital, With 46,Xy Sex Reversal",C566131,1,1
1,0,201,"Myopathy, Reducing Body, X-Linked, Early-Onset, Severe",C567469,1,1
1,0,201,"Cataract, Autosomal Recessive Congenital 3",C567835,1,1
1,0,201,"Hyperinsulinemic Hypoglycemia, Familial, 4",C566493,1,1
1,0,201,Capillariasis,D017189,1,1
1,0,201,"Cardiomyopathy, Dilated, 1V",C566856,1,1
1,0,201,Bleeding Disorder due to Defective Thromboxane A2 Receptor,C566055,1,1
1,0,201,Receptive aphasia (finding),D001041,1,1
1,0,201,"Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant",C566672,1,1
1,0,201,"Deafness, Autosomal Recessive 18",C566580,1,1
1,0,201,"Mental Retardation, Autosomal Dominant 1",C566947,3,1
1,0,201,Chromosome 1q43-Q44 Deletion Syndrome,C567346,3,1
1,0,201,AICARDI-GOUTIERES SYNDROME 3,C563683,1,1
1,0,201,JOUBERT SYNDROME 7,C566916,1,1
1,0,201,Microcephaly-Micromelia Syndrome,C565382,1,1
1,0,201,"Erythrocytosis, Familial, 3",C565221,1,1
1,0,201,SPINOCEREBELLAR ATAXIA 21,C537200,1,1
1,0,201,Gracile bone dysplasia,C537291,1,1
1,0,201,Acid Phosphatase Deficiency,C562645,1,1
1,0,201,"Osteopetrosis, Autosomal Recessive 4",C566933,1,1
1,0,201,"Muscular Dystrophy, Scapulohumeral",C562932,3,1
1,0,201,"Arrhythmogenic Right Ventricular Dysplasia, Familial, 10",C565707,1,1
1,0,201,"ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY",C567533,1,1
1,0,201,"Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant",C566813,1,1
1,0,201,Hidradenitis,D016575,1,1
1,0,201,"Cleft Palate, Isolated, And Mental Retardation",C566991,1,1
1,0,201,"Hemophagocytic lymphohistiocytosis, familial, 4",C537252,1,1
1,0,201,Prognathism,D011378,1,1
1,0,201,Hydroxykynureninuria,C536081,1,1
1,0,201,CORNEA PLANA 2,C565677,1,1
1,0,201,"Myopathy, Myofibrillar, Zasp-Related",C563718,1,1
1,0,201,Familial Sudden Death,C566172,1,1
1,0,201,MORM syndrome,C536984,1,1
1,0,201,RETINITIS PIGMENTOSA 35,C565206,1,1
1,0,201,Pontocerebellar Hypoplasia Type 2C,C567324,1,1
1,0,201,Ulnar-Fibular Ray Defect and Brachydactyly,C563905,1,1
1,0,201,Filippi syndrome,C538152,1,1
1,0,201,"Adenylate Kinase Deficiency, Hemolytic Anemia Due To",C567228,1,1
1,0,201,"Lead Poisoning, Nervous System",D020263,1,1
1,0,201,Anomia,D000849,1,1
1,0,201,Methylmalonic aciduria cblB type,C537361,2,1
1,0,201,Narcissism,D009289,1,1
1,0,201,"Exfoliative Ichthyosis, Autosomal Recessive, Ichthyosis Bullosa of Siemens-like",C564309,1,1
1,0,201,"CILIARY DYSKINESIA, PRIMARY, 3",C535278,1,1
1,0,201,"CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE B (disorder)",C564703,1,1
1,0,201,Macular corneal dystrophy Type II (disorder),C563270,1,1
1,0,201,"Rett Syndrome, Preserved Speech Variant",C564063,1,1
1,0,201,Dicarboxylicaminoaciduria,C536171,1,1
1,0,201,"Stress Disorders, Traumatic, Acute",D040701,1,1
1,0,201,Lissencephaly 3,C566908,1,1
1,0,201,"Fibrosis of Extraocular Muscles, Congenital, 3C",C567666,1,1
1,0,201,"SPASTIC PARAPLEGIA 32, AUTOSOMAL RECESSIVE",C566983,1,1
1,0,201,Cataract Hutterite type,C538286,1,1
1,0,201,"Multiple Carboxylase Deficiency, Juvenile-Onset",C565365,1,1
1,0,201,"DYSTONIA 2, TORSION, AUTOSOMAL RECESSIVE (disorder)",C538006,1,1
1,0,201,"Mental Retardation, X-Linked 16",C563139,1,1
1,0,201,"Charcot-Marie-Tooth disease, Type 4B2",C535421,2,1
1,0,201,Achromatopsia 5,C567759,1,1
1,0,201,"Coma, Post-Head Injury",D020207,1,1
1,0,201,HYPOTRICHOSIS 8,C566950,1,1
1,0,201,Three M Syndrome 2,C567862,1,1
1,0,201,Orstavik Lindemann Solberg syndrome,C537137,1,1
1,0,201,LEBER CONGENITAL AMAUROSIS 6 (disorder),C565327,1,1
1,0,201,MOYAMOYA DISEASE 2,C536992,1,1
1,0,201,"SPINAL MUSCULAR ATROPHY, DISTAL, CONGENITAL NONPROGRESSIVE (disorder)",C563981,1,1
1,0,201,Congenital ectodermal dysplasia of face,C536385,1,1
1,0,201,Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency,C563654,1,1
1,0,201,Adrenal hyperplasia 2,C538236,1,1
1,0,201,Tonic Pupil,D015845,1,1
1,0,201,Pulmonary Arteriovenous Fistulas,C562404,1,1
1,0,201,"Thrombocytopenia, X-Linked, Intermittent",C564053,1,1
1,0,201,Acalculous Cholecystitis,D042101,1,1
1,0,201,"Osteopoikilosis, Isolated",C563484,1,1
1,0,201,Rhabdoviridae Infections,D018353,1,1
1,0,201,"AUDITORY NEUROPATHY, AUTOSOMAL DOMINANT, 1",C563790,1,1
1,0,201,"Cardiomyopathy, Dilated, 1DD",C567725,1,1
1,0,201,"Spinocerebellar Ataxia, X-Linked 5",C567478,1,1
1,0,201,"Neuronopathy, Distal Hereditary Motor, Type Viib",C564362,1,1
1,0,201,"Gaucher Disease, Type IIIb",C565555,1,1
1,0,201,"Spastic paraplegia 13, autosomal dominant",C537485,1,1
1,0,201,"Chromosome 8, trisomy 8p",C538019,1,1
1,0,201,African swine fever,D000357,1,1
1,0,201,Spinocerebellar ataxia 14,C537196,1,1
1,0,201,"ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION",C535388,1,1
1,0,201,Superior Vena Cava Thrombosis,D013479,1,1
1,0,201,"46,Xy True Hermaphroditism, Sry-Related",C567575,1,1
1,0,201,"PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE",C567844,1,1
1,0,201,"MICROPHTHALMIA, SYNDROMIC 8",C537686,1,1
1,0,201,"Muscular dystrophy, limb-girdle, type 1A",C535906,1,1
1,0,201,"Xanthinuria, Type II",C566358,1,1
1,0,201,Cone-Rod Dystrophy 11,C563671,1,1
1,0,201,Martin-Probst Deafness-Mental Retardation Syndrome,C564495,1,1
1,0,201,"Cataract, Juvenile, With Microcornea And Glucosuria",C567434,1,1
1,0,201,"Hyperphenylalaninemia, Non-Pku Mild",C567494,1,1
1,0,201,"SPASTIC PARAPLEGIA 9, AUTOSOMAL DOMINANT (disorder)",C536868,1,1
1,0,201,"PARKINSON DISEASE 4, AUTOSOMAL DOMINANT LEWY BODY (disorder)",C565324,1,1
1,0,201,"CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H",C563740,1,1
1,0,201,Psychophysiologic Disorders,D011602,1,1
1,0,201,CONE-ROD DYSTROPHY 1 (disorder),C563469,1,1
1,0,201,"DEAFNESS, X-LINKED 1 (disorder)",C564433,1,1
1,0,201,Coxa Magna,D000070603,1,1
1,0,201,"Cerebral Palsy, Spastic Quadriplegic, 2",C567867,1,1
1,0,201,"Heart defect, tongue hamartoma and polysyndactyly",C535849,1,1
1,0,201,"Deafness, Autosomal Dominant 36",C564675,1,1
1,0,201,"Apolipoprotein E, Deficiency or Defect of",C566260,1,1
1,0,201,"Drug Metabolism, Poor, CYP2C19-Related",C563703,1,1
1,0,201,"TREMOR, HEREDITARY ESSENTIAL, 1",C536545,1,1
1,0,201,Lithiasis,D020347,1,1
1,0,201,Cardiac form of generalized glycogenosis,C536839,1,1
1,0,201,"Glycogen Storage Disease 0, Muscle",C566917,1,1
1,0,201,"Cardiac Malformation, Cleft Lip-Palate, Microcephaly and Digital Anomalies",C563414,1,1
1,0,201,"Coronary Sclerosis, Medial, of Infancy",C565944,1,1
1,0,201,Nevo syndrome (disorder),C536113,1,1
1,0,201,Neutrophil Immunodeficiency Syndrome,C564275,1,1
1,0,201,Enthesopathy,D000070676,1,1
1,0,201,Hyperostosis Cranialis Interna,C564168,1,1
1,0,201,"CARDIOMYOPATHY, DILATED, 1M",C564390,1,1
1,0,201,"DIABETES MELLITUS, NONINSULIN-DEPENDENT, 1 (disorder)",C563359,1,1
1,0,201,"Congenital Disorder Of Glycosylation, Type IIID",C564625,1,1
1,0,201,Retinitis Pigmentosa 11,C563991,1,1
1,0,201,"Osteopetrosis, Autosomal Recessive 5",C566883,1,1
1,0,201,"Hypouricemia, Renal, 2",C567426,1,1
1,0,201,"Adenoma, Chromophobe",D000238,1,1
1,0,201,"FEBRILE CONVULSIONS, FAMILIAL, 1 (disorder)",C565162,1,1
1,0,201,"Deafness, Autosomal Recessive 7",C563417,1,1
1,0,201,Chromosome 17q21.31 Deletion Syndrome,C566476,1,1
1,0,201,"ANEMIA, SIDEROBLASTIC, AND SPINOCEREBELLAR ATAXIA",C536358,1,1
1,0,201,Acrokeratoelastoidosis of Costa,C535653,1,1
1,0,201,Glycogen Storage Disease IIIB,C566890,1,1
1,0,201,Familial Hyperbeta- and Prebetalipoproteinemia,C566262,1,1
1,0,201,dopamine beta hydroxylase deficiency,C535600,1,1
1,0,201,Macrophagic myofasciitis,C537829,1,1
1,0,201,"Bartter syndrome, antenatal , type 2",C537651,1,1
1,0,201,"Lactase Deficiency, Congenital",C562600,1,1
1,0,201,Donnai-Barrow syndrome,C536390,1,1
1,0,201,Orthostatic intolerance,D054971,1,1
1,0,201,Kocher-Debre-Semelaigne syndrome,C537211,1,1
1,0,201,Stormorken Syndrome,C566108,1,1
1,0,201,"Cataract, Nuclear Total",C566156,1,1
1,0,201,"BARTTER SYNDROME, TYPE 4A",C566530,1,1
1,0,201,"Spastic Paraplegia, Ataxia, And Mental Retardation",C564378,1,1
1,0,201,SPINOCEREBELLAR ATAXIA 28,C537205,1,1
1,0,201,Pigmented Paravenous Chorioretinal Atrophy,C566801,1,1
1,0,201,"Deafness, Autosomal Recessive 30",C564624,1,1
1,0,201,"SPASTIC PARAPLEGIA 44, AUTOSOMAL RECESSIVE (disorder)",C567707,1,1
1,0,201,Renal dysplasia diffuse cystic,C537755,1,1
1,0,201,"DEAFNESS, AUTOSOMAL DOMINANT 16",C565832,1,1
1,0,201,Methylmalonic aciduria cblA type,C537360,1,1
1,0,201,Dermatomycoses,D003881,1,1
1,0,201,"Corticosteroid-Binding Globulin, Elevated",C566934,1,1
1,0,201,"Drug Metabolism, Poor, CYP2D6-Related",C563835,1,1
1,0,201,"DEAFNESS, AUTOSOMAL DOMINANT 5 (disorder)",C563410,5,1
1,0,201,"Achromatopsia incomplete, X-linked",C538165,1,1
1,0,201,Ochronosis,D009794,1,1
1,0,201,Deficiency of fructokinase,C538068,1,1
1,0,201,Malouf syndrome,C535703,1,1
1,0,201,Najjar syndrome,C535580,1,1
1,0,201,"Charcot-Marie-Tooth disease, Type 2B1",C537990,1,1
1,0,201,Lateral Sinus Thrombosis,D020227,1,1
1,0,201,"Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance",C537456,2,1
1,0,201,Pancreatoblastoma,C537162,1,1
1,0,201,Apudoma,D001079,1,1
1,0,201,Total intestinal aganglionosis,C538058,1,1
1,0,201,"Cryohydrocytosis, Stomatin-Deficient, with Mental Retardation, Seizures, Cataracts, and Massive Hepatosplenomegaly",C563840,1,1
1,0,201,"CARDIOMYOPATHY, DILATED, 2A (disorder)",C567505,1,1
1,0,201,Ehlers-Danlos syndrome caused by tenascin-X deficiency,C536193,1,1
1,0,201,"Hyperthyroidism, Familial Gestational",C566384,1,1
1,0,201,"DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, BASAL GANGLIA DISEASE, AND SEIZURES",C535773,1,1
1,0,201,"Osteopetrosis, Autosomal Recessive 1",C564915,1,1
1,0,201,Amyotrophic Lateral Sclerosis 10,C567429,1,1
1,0,201,"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 3",C563929,1,1
1,0,201,Fused Teeth,D005671,1,1
1,0,201,Familial pityriasis rubra pilaris,C531784,1,1
1,0,201,"Macrothrombocytopenia, Autosomal Dominant, Tubb1-Related",C567747,1,1
1,0,201,Cerebrovascular Trauma,D020214,1,1
1,0,201,"Camptosynpolydactyly, Complex",C564383,1,1
1,0,201,Glycogen Storage Disease XIII,C567861,1,1
1,0,201,"SPASTIC PARAPLEGIA 26, AUTOSOMAL RECESSIVE (disorder)",C536862,1,1
1,0,201,Epidural Abscess,D020802,1,1
1,0,201,Vulvar Diseases,D014845,1,1
1,0,201,"Heart-hand syndrome, Slovenian type",C535852,1,1
1,0,201,SPINOCEREBELLAR ATAXIA WITH EPILEPSY,C564395,1,1
1,0,201,"Wasting Disease, Chronic",D034081,1,1
1,0,201,"Asthma, Nasal Polyps, And Aspirin Intolerance",C565935,2,1
1,0,201,Foot Diseases,D005534,1,1
1,0,201,"Peroxisome Biogenesis Disorder, Complementation Group 12",C566405,1,1
1,0,201,Otitis Externa,D010032,1,1
1,0,201,"MECKEL SYNDROME, TYPE 5",C566915,1,1
1,0,201,Basan syndrome,C537659,1,1
1,0,201,Asphyxia,D001237,1,1
1,0,201,"Spastic Paraplegia, Optic Atrophy, and Neuropathy",C563702,1,1
1,0,201,NEPHRONOPHTHISIS 7,C566930,1,1
1,0,201,"Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis",C567195,1,1
1,0,201,JOUBERT SYNDROME 6,C537689,1,1
1,0,201,"CILIARY DYSKINESIA, PRIMARY, 11",C567212,1,1
1,0,201,"Dyskinesia, Familial, with Facial Myokymia",C564676,1,1
1,0,201,Polyposis Of Gastric Fundus Without Polyposis Coli,C566775,2,1
1,0,201,Branchio-skeleto-genital syndrome,C537084,1,1
1,0,201,"Cystinosis, Infantile Nephropathic",C565655,1,1
1,0,201,Megaloblastic Anemia due to Dihydrofolate Reductase Deficiency,C565095,1,1
1,0,201,Nocardia Infections,D009617,1,1
1,0,201,Behr syndrome,C537669,1,1
1,0,201,Colloid Cysts,D056364,1,1
1,0,201,"Peroxisome Biogenesis Disorder, Complementation Group J",C563965,1,1
1,0,201,Anauxetic dysplasia,C538256,1,1
1,0,201,"Cardiomyopathy, Familial Hypertrophic, 2",C566171,1,1
1,0,201,"Cardiomyopathy, Dilated, 1g",C565824,1,1
1,0,201,"CARDIOMYOPATHY, DILATED, 1N",C564388,1,1
1,0,201,"Spondyloepiphyseal dysplasia, Omani type",C535789,1,1
1,0,201,Richieri Costa Pereira syndrome,C535677,1,1
1,0,201,Food intolerance (disorder),D000073923,1,1
1,0,201,Catel Manzke syndrome,C535347,1,1
1,0,201,"Deafness, Autosomal Dominant 28",C563890,1,1
1,0,201,D-glycericacidemia,C535767,1,1
1,0,201,Juvenile-onset dystonia,C537704,1,1
1,0,201,"Pancreatitis, Graft",D055589,1,1
1,0,201,Lactate dehydrogenase deficiency type A,C538133,1,1
1,0,201,"Microphthalmia, Syndromic 5",C566441,1,1
1,0,201,"Thrombophilia, Hereditary, Due To Protein S Deficiency, Autosomal Dominant",C567347,1,1
1,0,201,"46,Xy Gonadal Dysgenesis, Complete, Sry-Related",C567574,1,1
1,0,201,"CARDIOMYOPATHY, DILATED, 1D (disorder)",C563306,1,1
1,0,201,Pyruvate Dehydrogenase E3-Binding Protein Deficiency,C565447,1,1
1,0,201,"Deafness, Autosomal Recessive 9",C563396,1,1
1,0,201,Spheroid body myopathy,C000598645,1,1
1,0,201,ICHTHYOSIS PREMATURITY SYNDROME,C536271,1,1
1,0,201,"Spastic paraplegia 3, autosomal dominant",C536864,1,1
1,0,201,"CILIARY DYSKINESIA, PRIMARY, 6",C567057,1,1
1,0,201,"Nystagmus 1, congenital, X- linked",C537853,1,1
1,0,201,X-linked myopathy with excessive autophagy,C564093,1,1
1,0,201,"Polymicrogyria, Asymmetric",C567658,1,1
1,0,202,Juvenile nephropathic cystinosis (disorder),C562683,2,1
1,0,202,Keshan disease,C536166,2,1
1,0,202,"Onchocerciasis, Ocular",D015827,4,1
1,0,202,Epilepsia Partialis Continua,D017036,3,1
1,0,202,"Deafness, Sensorineural, Autosomal-Mitochondrial Type",C565637,3,1
1,0,202,"PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE (disorder)",C538104,2,1
1,0,202,"Kenny-Caffey syndrome, type 2",C537020,2,1
1,0,202,Foley-Denny-Brown Syndrome,D009468,2,1
1,0,202,"2,4-Dienoyl-CoA Reductase Deficiency",C565624,2,1
1,0,202,"DIABETES MELLITUS, INSULIN-DEPENDENT, 8",C563433,2,1
1,0,202,Desmosterolosis,C566555,2,1
1,0,202,Ectodermal dysplasia/ skin fragility syndrome,C536183,2,1
1,0,202,"MICROCEPHALY, PRIMARY AUTOSOMAL RECESSIVE, 1",C565384,2,1
1,0,202,Picornaviridae Infections,D010850,2,1
1,0,202,Chromosome 17p Deletion Syndrome,C538045,2,1
1,0,202,Polymicrogyria With Optic Nerve Hypoplasia,C567715,2,1
1,0,202,North Carolina macular dystrophy,C537835,5,1
1,0,202,Presbycusis,D011304,2,1
1,0,202,Nevus of Ota,D009507,3,1
1,0,202,"KENNY-CAFFEY SYNDROME, TYPE 1",C537021,2,1
1,0,202,"Hemangiopericytoma, Malignant",C562740,2,1
1,0,202,Cri-du-Chat Syndrome,D003410,5,1
1,0,202,"Peroxisomal Dysfunction, General",D018901,2,1
1,0,202,Diamond-Blackfan Anemia 5,C567280,2,1
1,0,202,Pelvic Cancer,D010386,2,1
1,0,202,Dihydropyrimidine Dehydrogenase Deficiency,D054067,3,1
1,0,202,"Congenital Disorder Of Glycosylation, Type IIF",C567040,2,1
1,0,202,Propionicaciduria,D056693,2,1
1,0,202,Oligosynaptic Infertility,C562902,2,1
1,0,202,Cancer-Associated Retinopathy,D059545,3,1
1,0,202,"SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT (disorder)",C536866,2,1
1,0,202,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE, WITH AXONAL NEUROPATHY",C537313,2,1
1,0,202,Platelet aggregation,D010974,5,1
1,0,202,Lujan Fryns syndrome,C537724,3,1
1,0,202,CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS (disorder),C567401,2,1
1,0,202,Adjustment Disorders,D000275,2,1
1,0,202,"Impotence, Vasculogenic",D018783,3,1
1,0,202,Complement Component 6 Deficiency,C567307,2,1
1,0,202,Temporomandibular ankylosis,C536957,2,1
1,0,202,Alagille Syndrome 1,D016738,2,1
1,0,202,Medullary Cystic Kidney Disease Type 2,C548033,2,1
1,0,202,Spondyloepimetaphyseal dysplasia with multiple dislocations,C535784,2,1
1,0,202,Mulibrey Nanism,D050336,2,1
1,0,202,Inherited Thyroxine-Binding Globulin Deficiency,C580199,2,1
1,0,202,Myxedema,D009230,2,1
1,0,202,Pulmonary Alveolar Microlithiasis,C562405,2,1
1,0,202,PRESENILE AND SENILE DEMENTIA,C563254,2,1
1,0,202,"MUSCULAR DYSTROPHY, CONGENITAL, 1C",C564691,2,1
1,0,202,Potassium Deficiency,D011191,2,1
1,0,202,Thyroxine-Binding Globulin Deficiency,C564049,2,1
1,0,202,Congenital alopecia X-linked,C535981,2,1
1,0,202,WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME,C536708,2,1
1,0,202,BARDET-BIEDL SYNDROME 14 (disorder),C567141,2,1
1,0,202,Woodhouse Sakati syndrome,C536742,2,1
1,0,202,CONE DYSTROPHY 3 (disorder),C566579,2,1
1,0,202,Pontocerebellar Hypoplasia Type 6,C548074,2,1
1,0,202,Marcus Gunn phenomenon,C535908,2,1
1,0,202,"Iris Coloboma with Ptosis, Hypertelorism, and Mental Retardation",C565462,2,1
1,0,202,Premature Ejaculation,D061686,2,1
1,0,202,Corticosterone Methyl Oxidase Type I Deficiency,C537806,2,1
1,0,202,Malignant neoplasm of sigmoid colon,D012811,2,1
1,0,202,Cole Carpenter syndrome,C535963,2,1
1,0,202,"Pyruvate Dehydrogenase Complex Deficiency Disease, Neonatal",D015325,2,1
1,0,202,"DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT",C565079,2,1
1,0,202,"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2K",C535418,2,1
1,0,202,Monosomy 5p,C538482,2,1
1,0,202,"Infections, Arenavirus",D001117,3,1
1,0,202,Harding ataxia,C535633,2,1
1,0,202,Primary lateral sclerosis juvenile,C536416,2,1
1,0,202,Cerebral Venous Angioma,D020787,2,1
1,0,202,Hecht syndrome (disorder),C535857,2,1
1,0,202,"Spondylocostal Dysostosis 4, Autosomal Dominant",C565149,2,1
1,0,202,"Chromosome 5, monosomy 5q35",C537647,2,1
1,0,202,BORNHOLM EYE DISEASE,C564092,3,1
1,0,202,"Tachycardia, Ectopic Junctional",D013613,2,1
1,0,202,"Congenital Disorder Of Glycosylation, Type IIB",C565264,2,1
1,0,202,Facial Hemiatrophy,D005150,2,1
1,0,202,Neurothekeoma,D018321,2,1
1,0,202,Congenital disorder of glycosylation type 1G,C535745,2,1
1,0,202,Senior-Loken Syndrome 5,C563763,2,1
1,0,202,"Chondrodysplasia, Megarbane-Dagher-Melki Type",C567644,2,1
1,0,202,"MENTAL RETARDATION, X-LINKED 3",C563136,2,1
1,0,202,Anoxia of brain,D002534,2,1
1,0,202,"Congenital Disorder Of Glycosylation, Type IIH",C566987,2,1
1,0,202,Congenital disorder of glycosylation type 1X,C535751,2,1
1,0,202,Arrhinia,C537438,2,1
1,0,202,CAPOS syndrome,C535351,2,1
1,0,202,Calcium Metabolism Disorders,D002128,2,1
1,0,202,Sleep Latency,D000074361,3,1
1,0,202,"Epidermolysis bullosa, lethal acantholytic",C535493,2,1
1,0,202,Congenital disorder of glycosylation type 1L,C535750,2,1
1,0,202,Van Maldergem Wetzburger Verloes syndrome,C536530,2,1
1,0,202,Renal hepatic pancreatic dysplasia Dandy Walker cyst,C537756,2,1
1,0,202,Retinal cone dystrophy 2,C538363,2,1
1,0,202,"Arrhythmogenic Right Ventricular Dysplasia, Familial, 9",C563808,4,1
1,0,202,"Peroxisome Biogenesis Disorder, Complementation Group 7",C566422,2,1
1,0,202,"ATAXIA, SPASTIC, 1, AUTOSOMAL DOMINANT",C566993,2,1
1,0,202,Postoperative Residual Curarization,D055191,2,1
1,0,202,"Anemia, Diamond-Blackfan, 2",C536130,3,1
1,0,202,"Microphthalmia, syndromic 1",C537464,4,1
1,0,202,Uterine Cervicitis,D002575,2,1
1,0,202,"Colonic Diseases, Functional",D003109,2,1
1,0,202,"Angiomatosis, Bacillary",D016917,2,1
1,0,202,Lymphedema distichiasis syndrome,C537710,2,1
1,0,202,Arginine:Glycine Amidinotransferase Deficiency,C567192,2,1
1,0,202,"Cystinuria, Type B",C565652,2,1
1,0,202,"CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1",C564258,2,1
1,0,202,"EPILEPSY, PROGRESSIVE MYOCLONIC 2B",C564976,2,1
1,0,202,Broca Aphasia,D001039,2,1
1,0,202,Traumatic Brain Injury,D000070642,2,1
1,0,202,Dyschromatosis universalis hereditaria,C535730,4,1
1,0,202,"Cataract, posterior polar, 3",C535343,2,1
1,0,202,"Acquired Metabolic Diseases, Nervous System",D001928,2,1
1,0,202,Hypotrichosis And Recurrent Skin Vesicles,C567751,2,1
1,0,202,Social Communication Disorder,D000067404,5,1
1,0,202,Meckel syndrome type 3,C536132,3,1
1,0,202,"Keratosis Follicularis Spinulosa Decalvans, X-Linked",C536159,2,1
1,0,202,Combined Oxidative Phosphorylation Deficiency 3,C566467,2,1
1,0,202,Magnesium Deficiency,D008275,3,1
1,0,202,"Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 2",C567656,3,1
1,0,202,Choroidal sclerosis,C535358,2,1
1,0,202,"Adrenal Insufficiency, Congenital",C566130,2,1
1,0,202,"Mental Retardation, X-Linked 45",C564503,3,1
1,0,202,"Porphyria Cutanea Tarda, Type I",C566768,2,1
1,0,202,Lethal tight skin contracture syndrome (disorder),C536920,4,1
1,0,202,Oliver-McFarlane syndrome,C536554,2,1
1,0,202,Symphysis Pubis Dysfunction,D059388,7,1
1,0,202,Acrocephalopolysyndactyly type 2,C563187,4,1
1,0,202,Brachydactyly with hypertension,C537095,2,1
1,0,202,MAST SYNDROME,C565409,2,1
1,0,202,Herpes Labialis,D006560,2,1
1,0,202,"CONE DYSTROPHY, X-LINKED, 1",C564439,3,1
1,0,202,Lassa Fever,D007835,2,1
1,0,202,"Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation",C566970,2,1
1,0,202,OROFACIAL CLEFT 10,C566605,2,1
1,0,202,Muscle Disease Manifestations,D020879,2,1
1,0,202,"FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3B (disorder)",C567739,2,1
1,0,202,Cerebrofrontofacial Syndrome,C563904,2,1
1,0,202,"Alzheimer Disease, Early-Onset, With Cerebral Amyloid Angiopathy",C566299,2,1
1,0,202,HTLV-II Infections,D015491,7,1
1,0,202,Nager syndrome,C538184,2,1
1,0,202,Benign essential blepharospasm,C535428,3,1
1,0,202,Histidinuria renal tubular defect,C538321,2,1
1,0,202,Glycogen Storage Disease XIV,C567859,2,1
1,0,202,PARTINGTON X-LINKED MENTAL RETARDATION SYNDROME,C536300,2,1
1,0,202,Gastric Antral Vascular Ectasia,D020252,3,1
1,0,202,LIG4 Syndrome,C564694,2,1
1,0,202,"Congenital Disorder Of Glycosylation, Type Im",C563666,2,1
1,0,202,"Hyperuricemic Nephropathy, Familial Juvenile 2",C567760,2,1
1,0,202,Spastic Paraplegia Type 4,C580456,3,1
1,0,202,Congenital absence of thymus,C536288,3,1
1,0,202,HEREDITARY RENAL CANCER ASSOCIATED 1,C564169,2,1
1,0,202,Aminoacylase 1 deficiency,C538246,2,1
1,0,202,Atkin syndrome,C538195,3,1
1,0,202,"Charcot-Marie-Tooth Disease, Dominant Intermediate C",C564257,2,1
1,0,202,Cadmium poisoning,D002105,2,1
1,0,202,Neural tube defects X-linked,C536410,6,1
1,0,202,"PARKINSON DISEASE 7, AUTOSOMAL RECESSIVE EARLY-ONSET",C565238,2,1
1,0,202,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 5",C537311,2,1
1,0,202,Michelin tire baby syndrome,C537575,2,1
1,0,202,"Chromosome 3, monosomy 3p25",C536807,3,1
1,0,202,Beta-Hydroxyisobutyryl CoA Deacylase Deficiency,C562803,2,1
1,0,202,HEM dysplasia,C535858,2,1
1,0,202,Vesicovaginal Fistula,D014719,2,1
1,0,202,Severe combined immunodeficiency with sensitivity to ionizing radiation,C537589,2,1
1,0,202,Combined Oxidative Phosphorylation Deficiency 5,C567126,2,1
1,0,202,Ataxia-Telangiectasia Variant,C566865,2,1
1,0,202,Osteoma,D010016,2,1
1,0,202,"CORNEAL DYSTROPHY, POSTERIOR AMORPHOUS",C567546,2,1
1,0,202,"Leukoencephalopathy, Cystic, Without Megalencephaly",C567845,2,1
1,0,202,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 9",C567436,2,1
1,0,202,Very long chain acyl-CoA dehydrogenase deficiency,C536353,3,1
1,0,202,Lichen Simplex Chronicus,D009450,2,1
1,0,202,Synpolydactyly 3,C565216,2,1
1,0,202,Exhibitionism,D005084,2,1
1,0,202,6-pyruvoyl-tetrahydropterin synthase deficiency,C535325,2,1
1,0,202,gamma-Glutamyltransferase deficiency,C536836,2,1
1,0,202,Glycogen Storage Disease IXC,C567809,2,1
1,0,202,Coumarin Sensitivity,C567276,2,1
1,0,202,"GRISCELLI SYNDROME, TYPE 2",C537302,3,1
1,0,202,"Spina Bifida, X-Linked",C564459,5,1
1,0,202,Pallister-Killian syndrome,C538105,3,1
1,0,202,LETHAL CONGENITAL CONTRACTURAL SYNDROME 3,C566961,2,1
1,0,202,"Microcephaly, Primary Autosomal Recessive, 5",C563871,2,1
1,0,202,Split-Hand-Foot Malformation With Long Bone Deficiency 1,C536425,2,1
1,0,202,Favism,D005236,2,1
1,0,202,"Leukodystrophy, Hypomyelinating, 4",C567390,2,1
1,0,202,"Deafness, Autosomal Dominant 12",C563295,2,1
1,0,202,Meigs Syndrome,D008539,2,1
1,0,202,"HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY",C562793,2,1
1,0,202,Combined Oxidative Phosphorylation Deficiency 2,C566468,2,1
1,0,202,Blepharo-cheilo-dontic syndrome,C536188,2,1
1,0,202,"Mesothelioma, Cystic",D018261,4,1
1,0,202,succinic semialdehyde dehydrogenase deficiency,C535803,3,1
1,0,202,Subacute thyroiditis,D013968,2,1
1,0,202,Hydroxylysinuria,C565502,2,1
1,0,202,SENIOR-LOKEN SYNDROME 4,C537581,2,1
1,0,202,"Hypospadias 1, X-Linked",C567482,2,1
1,0,202,MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS,C536141,6,1
1,0,202,"Porphyria, South African type",C538659,2,1
1,0,202,"Leukokeratosis, Hereditary Mucosal",D053529,2,1
1,0,202,"Hereditary orotic aciduria, type 1",C537136,2,1
1,0,202,Renal hypouricemia,C537757,3,1
1,0,202,Watermelon stomach disease,C538665,2,1
1,0,202,"DEAFNESS, AUTOSOMAL DOMINANT 25 (disorder)",C565319,2,1
1,0,202,"USHER SYNDROME, TYPE ID",C563400,2,1
1,0,202,Dent Disease 2,C564487,2,1
1,0,202,Dentinogenesis imperfecta - Shield's type III (disorder),C538216,3,1
1,0,202,"Methylcobalamin Deficiency, CblG Type",C565394,2,1
1,0,202,NORTH AMERICAN INDIAN CHILDHOOD CIRRHOSIS,C565737,2,1
1,0,202,Opitz trigonocephaly syndrome,C537418,2,1
1,0,202,Osteochondrosis,D055034,2,1
1,0,202,"MENTAL RETARDATION, X-LINKED 34 (disorder)",C563148,3,1
1,0,202,Digitorenocerebral Syndrome,C563052,3,1
1,0,202,Bardet-Biedl syndrome 4 (disorder),C537912,2,1
1,0,202,"Usher syndrome, type 1F",C536489,2,1
1,0,202,Oto-Palato-digital syndrome type 1,C536065,2,1
1,0,202,Colpocephaly,C535973,5,1
1,0,202,Thiamine responsive megaloblastic anemia syndrome,C536510,2,1
1,0,202,Johanson-Blizzard syndrome,C535880,3,1
1,0,202,"Sucrase-isomaltase deficiency, congenital",C538139,2,1
1,0,202,BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 1,C567618,2,1
1,0,202,Ehlers-Danlos syndrome 6B,C536192,3,1
1,0,202,"Alpha-Thalassemia Mental Retardation Syndrome, Deletion-Type",C563050,2,1
1,0,202,Multiple Carboxylase Deficiency,D009100,2,1
1,0,202,Dent disease 1,C538212,2,1
1,0,202,"Liver Abscess, Amebic",D008101,3,1
1,0,202,Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects,C562515,3,1
1,0,202,"SPINAL MUSCULAR ATROPHY, TYPE IV",C563948,2,1
1,0,202,"Mental Retardation, Autosomal Dominant 5",C567234,4,1
1,0,202,Adenosine monophosphate deaminase deficiency,C538234,2,1
1,0,202,"BARTTER SYNDROME, TYPE 4B",C567762,2,1
1,0,202,Fascioliasis,D005211,4,1
1,0,202,"CITRULLINEMIA, TYPE II, NEONATAL-ONSET",C536398,2,1
1,0,202,Borderline leprosy,D015439,2,1
1,0,202,Trematode Infections,D014201,2,1
1,0,202,"Mental Retardation, X-Linked 9",C563137,3,1
1,0,202,Congenital disorder of glycosylation type 1J,C535748,2,1
1,0,202,Diastema of Teeth,D003970,6,1
1,0,202,"Coloboma, Ocular, And Ichthyosis, Brain Malformations, And Endocrine Abnormalities",C567328,2,1
1,0,202,"SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE (disorder)",C564811,2,1
1,0,202,Retinitis Pigmentosa 25,C566425,2,1
1,0,202,Hyperventilation,D006985,7,1
1,0,202,WOLFRAM SYNDROME 2,C565733,3,1
1,0,202,"Mental Retardation, X-Linked 58",C564566,3,1
1,0,202,Hereditary Myopathy with Early Respiratory Failure,C566343,2,1
1,0,202,Cone-Rod Dystrophy 7,C566350,2,1
1,0,202,"Glycogen Storage Disease, Type IXD",C564485,2,1
1,0,202,"Woolly Hair, Autosomal Recessive",C564735,2,1
1,0,202,SENIOR-LOKEN SYNDROME 6,C565708,2,1
1,0,202,"Chorea, Benign Familial",C565851,2,1
1,0,202,Vitamin E Deficiency,D014811,3,1
1,0,202,Keratolytic winter erythema,C536155,2,1
1,0,202,"Pigmented Nodular Adrenocortical Disease, Primary, 2",C566472,2,1
1,0,202,Contiguous Abcd1-Dxs1375e Deletion Syndrome,C564508,2,1
1,0,202,"MALE PSEUDOHERMAPHRODITISM: DEFICIENCY OF TESTICULAR 17,20-DESMOLASE",C564109,2,1
1,0,202,Pick Complex,C563966,2,1
1,0,202,"DEAFNESS, AMINOGLYCOSIDE-INDUCED",C564013,3,1
1,0,202,Deafness enamel hypoplasia nail defects,C535994,2,1
1,0,202,Familial Osteochondritis Dissecans,C580095,3,1
1,0,202,Anodontia of Permanent Dentition,C563203,7,1
1,0,202,Retinitis Pigmentosa 10,C566715,2,1
1,0,202,"Congenital disorder of glycosylation, type 2G",C535756,2,1
1,0,202,Chromosome 17p13.3 Duplication Syndrome,C567705,2,1
1,0,202,"Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive",C567145,2,1
1,0,202,"Congenital Disorder of Glycosylation, Type Io",C567857,2,1
1,0,202,"Mandibulofacial dysostosis, Treacher Collins type, autosomal recessive",C535707,2,1
1,0,202,RENAL-HEPATIC-PANCREATIC DYSPLASIA,C567142,2,1
1,0,202,"Usher syndrome, type 1D",C536487,2,1
1,0,202,Linear IgA Bullous Dermatosis,D062027,3,1
1,0,202,Congenital disorder of glycosylation type 2D,C535753,2,1
1,0,202,Retinitis Pigmentosa 18,C563320,2,1
1,0,202,"ICHTHYOSIS, LAMELLAR, 3",C537265,2,1
1,0,202,"Transposition of the Great Arteries, Dextro-Looped 1",C563853,5,1
1,0,202,Hand foot uterus syndrome,C535627,2,1
1,0,202,CAMPTODACTYLY-ARTHROPATHY-COXA VARA-PERICARDITIS SYNDROME,C537560,3,1
1,0,202,"POLYPOSIS SYNDROME, HEREDITARY MIXED, 1",C563365,3,1
1,0,202,"DYSTONIA 4, TORSION, AUTOSOMAL DOMINANT (disorder)",C538004,2,1
1,0,202,LEBER OPTIC ATROPHY AND DYSTONIA,C536024,2,1
1,0,202,"GRISCELLI SYNDROME, TYPE 3",C537303,2,1
1,0,202,Infantile onset spinocerebellar ataxia,C535523,2,1
1,0,202,"47, XYY syndrome",C535317,2,1
1,0,202,NEPHRONOPHTHISIS 3,C565780,2,1
1,0,202,"HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC (disorder)",C565261,2,1
1,0,202,Bilateral Vestibulopathy,D000071699,2,1
1,0,202,"NONCOMPACTION OF LEFT VENTRICULAR MYOCARDIUM, FAMILIAL ISOLATED, AUTOSOMAL DOMINANT 1",C565821,2,1
1,0,202,3-Hydroxyisobutyric aciduria,C535312,2,1
1,0,202,"Usher syndrome, type 1C",C536486,2,1
1,0,202,TYLOSIS WITH ESOPHAGEAL CANCER,C536164,2,1
1,0,202,Anisocoria,D015875,2,1
1,0,202,"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I",C564612,2,1
1,0,202,"Lactic Acidosis, Congenital Infantile, Due To Lad Deficiency",C573012,2,1
1,0,202,XFE Progeroid Syndrome,C567043,2,1
1,0,202,Ascorbic Acid Deficiency,D001206,3,1
1,0,202,Posterior column ataxia,C536342,2,1
1,0,202,Mucolipidosis III Gamma,C565367,2,1
1,0,202,Ebstein Anomaly,D004437,2,1
1,0,202,alpha-Mannosidosis,D008363,4,1
1,0,202,Zika Virus Infection,D000071243,4,1
1,0,202,Congenital disorder of glycosylation type 2E,C535754,2,1
1,0,202,RHYNS syndrome,C537612,2,1
1,0,202,"Inclusion body myopathy, autosomal dominant",C538330,2,1
1,0,202,Mobius II syndrome,C531747,2,1
1,0,202,Adenylosuccinate lyase deficiency (disorder),C538235,2,1
1,0,202,HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME,C537157,3,1
1,0,202,Hepatoerythropoietic Porphyria,D017121,3,1
1,0,202,"SPASTIC PARAPLEGIA 2, X-LINKED (disorder)",C536857,3,1
1,0,202,"Polycystic kidneys, severe infantile with tuberous sclerosis",C536328,2,1
1,0,202,Optic Disk Drusen,D015594,3,1
1,0,202,Congenital disorder of glycosylation type 1K,C535749,2,1
1,0,202,Combined Oxidative Phosphorylation Deficiency 4,C565690,2,1
1,0,203,"Brain Diseases, Metabolic, Inborn",D020739,4,1
1,0,203,Fetal hydantoin syndrome,C537922,4,1
1,0,203,"Xanthinuria, Type I",C562584,4,1
1,0,203,"Maple Syrup Urine Disease, Type IA",C535710,3,1
1,0,203,Motion Sickness,D009041,15,1
1,0,203,After-cataract,D058442,5,1
1,0,203,Growth Deficiency and Mental Retardation with Facial Dysmorphism,C565358,3,1
1,0,203,"Dyskeratosis Congenita, Autosomal Recessive",C565611,3,1
1,0,203,"Hypercholanemia, Familial",C564336,3,1
1,0,203,"Anemia, hereditary spherocytic hemolytic",C536356,3,1
1,0,203,Angiomyoma,D018229,3,1
1,0,203,Calcification of Joints and Arteries,C565891,3,1
1,0,203,Mucopolysaccharidosis VII,D016538,3,1
1,0,203,NF1 Microdeletion Syndrome,C563524,3,1
1,0,203,Aphonia,D001044,3,1
1,0,203,Cysticercosis,D003551,3,1
1,0,203,Deoxyguanosine Kinase Deficiency,C580039,3,1
1,0,203,Hirschsprung disease 1,C538540,5,1
1,0,203,"ALZHEIMER DISEASE, FAMILIAL, 1",C566298,4,1
1,0,203,"MAPLE SYRUP URINE DISEASE, TYPE II",C535712,3,1
1,0,203,Phosphoglycerate Kinase 1 Deficiency,C567067,3,1
1,0,203,"Lactic Acidosis, Fatal Infantile",C566885,3,1
1,0,203,Blood Group Incompatibility,D001787,3,1
1,0,203,Pili Torti,C562485,8,1
1,0,203,Hereditary Non-Polyposis Colon Cancer Type 2,D055847,3,1
1,0,203,"Hyperaldosteronism, Familial, Type II",C565312,3,1
1,0,203,Guanidinoacetate methyltransferase deficiency,C537622,3,1
1,0,203,"HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 1",C576976,5,1
1,0,203,"Heterotopia, Periventricular, Autosomal Recessive",C564292,3,1
1,0,203,"FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 2",C566587,3,1
1,0,203,Hypotrichosis Simplex of Scalp,C564143,3,1
1,0,203,Persian Gulf Syndrome,D018923,3,1
1,0,203,Lactose Intolerance,D007787,5,1
1,0,203,Familial juvenile gout,C537696,4,1
1,0,203,"Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, NK Cell-Positive",C563311,3,1
1,0,203,"SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE",C564599,4,1
1,0,203,Splenic Diseases,D013158,3,1
1,0,203,Focal Epithelial Hyperplasia,D017573,3,1
1,0,203,Discitis,D015299,4,1
1,0,203,Paraneoplastic Encephalomyelitis,D020361,4,1
1,0,203,Congenital disorder of glycosylation type 1C,C535741,3,1
1,0,203,Primary hypomagnesemia (disorder),C537153,3,1
1,0,203,"Osteopetrosis, Autosomal Recessive 6",C566931,3,1
1,0,203,Tubulointerstitial nephritis and uveitis,C536922,3,1
1,0,203,"Xeroderma pigmentosum, variant type",C536766,3,1
1,0,203,Burn-Mckeown syndrome,C537411,3,1
1,0,203,Combined Oxidative Phosphorylation Deficiency 1,C563797,3,1
1,0,203,"TOE SYNDACTYLY, TELECANTHUS, AND ANOGENITAL AND RENAL MALFORMATIONS",C567475,4,1
1,0,203,Combined molybdoflavoprotein enzyme deficiency,C535811,3,1
1,0,203,Hemorrhoids,D006484,3,1
1,0,203,Hyperlysinemias,D020167,3,1
1,0,203,"Short rib-polydactyly syndrome, Beemer type",C537599,3,1
1,0,203,"Spina Bifida, Folate-Sensitive",C566648,6,1
1,0,203,Cholesterol Ester Storage Disease,D015217,3,1
1,0,203,"Microcephaly with Chorioretinopathy, Autosomal Recessive",C565379,3,1
1,0,203,Fumarase deficiency,C538191,4,1
1,0,203,Brachytelephalangic Chondrodysplasia Punctata,C535941,3,1
1,0,203,Naxos disease,C538346,3,1
1,0,203,Neu-Laxova syndrome,C536405,4,1
1,0,203,Diamond-Blackfan Anemia 1,C567302,3,1
1,0,203,Amyopathic dermatomyositis,C538250,3,1
1,0,203,"HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 3",C537251,3,1
1,0,203,3-methylcrotonyl CoA carboxylase 1 deficiency,C535308,5,1
1,0,203,"17,20-Lyase Deficiency, Isolated",C567076,3,1
1,0,203,Testicular Microlithiasis,C566478,3,1
1,0,203,Lynch syndrome I (site-specific colonic cancer),C537261,3,1
1,0,203,Tn Syndrome,C562719,3,1
1,0,203,Ornithine carbamoyltransferase deficiency,D020163,9,1
1,0,203,"Mental Retardation, X-Linked 63",C564522,3,1
1,0,203,"Eye Diseases, Hereditary",D015785,7,1
1,0,203,MUCOLIPIDOSIS II ALPHA/BETA (disorder),C567100,3,1
1,0,203,"Macular dystrophy, concentric annular",C537833,3,1
1,0,203,"Vitamin D-dependent rickets, type 1",C562688,3,1
1,0,203,Congenital disorder of glycosylation type 1B,C535740,4,1
1,0,203,No-Reflow Phenomenon,D054318,3,1
1,0,203,Sulfite oxidase deficiency,C538141,3,1
1,0,203,PITT-HOPKINS SYNDROME,C537403,3,1
1,0,203,MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA (disorder),C564969,4,1
1,0,203,Glycogen Storage Disease Type VIII,D006015,3,1
1,0,203,"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id",C535742,3,1
1,0,203,Bulla,D001768,4,1
1,0,203,Neurodegeneration Due To Cerebral Folate Transport Deficiency,C567791,3,1
1,0,203,Heinz Body Anemias,C563030,3,1
1,0,203,X-Linked Infantile Nystagmus,C580539,3,1
1,0,203,COACH syndrome,C536430,3,1
1,0,203,Neisseriaceae Infections,D016870,3,1
1,0,203,Familial cerebral cavernous malformation,C536610,3,1
1,0,203,Hereditary Coproporphyria,D046349,4,1
1,0,203,"Mental Retardation, X-Linked 46",C564513,5,1
1,0,203,"MICROCEPHALY, PRIMARY AUTOSOMAL RECESSIVE, 7 (disorder)",C567198,3,1
1,0,203,Hiccup,D006606,3,1
1,0,203,Whipple Disease,D008061,4,1
1,0,203,"Microcephaly, Primary Autosomal Recessive, 6",C564247,3,1
1,0,203,"Abnormalities, Drug-Induced",D000014,5,1
1,0,203,"Maple syrup urine disease, type 1B",C535711,3,1
1,0,203,Renpenning syndrome 1,C537761,3,1
1,0,203,"Usher syndrome, type 2C",C536492,3,1
1,0,203,Speech Sound Disorders,D066229,4,1
1,0,203,"Cutis Laxa, Autosomal Recessive, Type IIA",C562632,3,1
1,0,203,Bile Reflux,D001655,4,1
1,0,203,Achromatopsia 2,C536128,3,1
1,0,203,Familial encephalopathy with neuroserpin inclusion bodies,C536841,4,1
1,0,203,Diamond-Blackfan Anemia With Microtia And Cleft Palate,C565256,3,1
1,0,203,Argininosuccinic Aciduria,D056807,4,1
1,0,203,"CHORIORETINAL ATROPHY, PROGRESSIVE BIFOCAL",C535356,3,1
1,0,203,JOUBERT SYNDROME 4 (disorder),C536296,3,1
1,0,203,"Reticuloendotheliosis, familial, with eosinophilia",C538564,3,1
1,0,203,Mainzer-Saldino Disease,C535463,4,1
1,0,203,Glycogen Storage Disease Type III,D006010,5,1
1,0,203,CAMFAK syndrome,C537965,4,1
1,0,203,Harderoporphyria,C562816,4,1
1,0,203,Pseudobulbar Palsy,D020828,4,1
1,0,203,Glycosylphosphatidylinositol deficiency,C537277,3,1
1,0,203,Megaduodenum and-or Megacystis,C563597,3,1
1,0,203,ALZHEIMER DISEASE 4,C536596,3,1
1,0,203,Congenital disorder of glycosylation type 1H,C535746,3,1
1,0,203,Martsolf syndrome,C536028,3,1
1,0,203,Brown-Vialetto-Van Laere syndrome,C537111,4,1
1,0,203,"Gout, HPRT-Related",C562583,3,1
1,0,203,"MENTAL RETARDATION, X-LINKED 72",C564547,3,1
1,0,203,Iritis,D007500,4,1
1,0,203,"Bartter syndrome, antenatal type 1",C537652,3,1
1,0,203,Dwarfism tall vertebrae,C535725,3,1
1,0,203,Cone-Rod Dystrophy 5,C563415,3,1
1,0,203,Glucose-6-phosphate transport defect,C562594,3,1
1,0,203,MITOCHONDRIAL MYOPATHY AND SIDEROBLASTIC ANEMIA,C536101,3,1
1,0,203,Stargardt disease 4,C535521,3,1
1,0,203,"Hyperglycinemia, Transient Neonatal",C562672,3,1
1,0,203,"Stress Disorders, Traumatic",D040921,4,1
1,0,203,Purine-nucleoside phosphorylase deficiency,C562587,4,1
1,0,203,Muscle Fatigue,D018763,4,1
1,0,203,Calcium pyrophosphate arthropathy,C563162,4,1
1,0,203,Arterial calcification of infancy,C537440,3,1
1,0,203,3-Methylglutaconic aciduria type 3,C535311,6,1
1,0,203,Enterocutaneous Fistula,D007412,3,1
1,0,203,"Congenital Disorder Of Glycosylation, Type In",C567437,4,1
1,0,203,Medium-chain acyl-coenzyme A dehydrogenase deficiency,C536038,7,1
1,0,203,CEREBRAL CAVERNOUS MALFORMATIONS 2,C566394,3,1
1,0,203,Wrinkly skin syndrome,C536750,4,1
1,0,203,Renal carnitine transport defect,C536778,11,1
1,0,203,"Dermatitis, Occupational",D009783,4,1
1,0,203,Holocarboxylase Synthetase Deficiency,D028922,3,1
1,0,203,"Neutropenia, Severe Congenital, X-Linked",C564539,3,1
1,0,203,"LEBER CONGENITAL AMAUROSIS, TYPE II (disorder)",C536601,5,1
1,0,203,"Leukodystrophy, Hypomyelinating, with Hypodontia and Hypogonadotropic Hypogonadism",C567313,4,1
1,0,203,Encephalocraniocutaneous lipomatosis,C535736,3,1
1,0,203,Oculovestibuloauditory syndrome,D055952,4,1
1,0,203,"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1B (disorder)",C535898,4,1
1,0,203,"Paget's Disease, Mammary",D010144,3,1
1,0,203,Tooth Diseases,D014076,3,1
1,0,203,ALPHA-KETOGLUTARATE DEHYDROGENASE DEFICIENCY,C536582,3,1
1,0,203,"Spastic paraplegia 15, autosomal recessive",C536642,3,1
1,0,203,"Chondrodysplasia Punctata, Rhizomelic",D018902,3,1
1,0,203,"KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT (disorder)",C567553,4,1
1,0,203,"Deafness, Autosomal Recessive 12",C563327,3,1
1,0,203,"Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis",C564570,3,1
1,0,203,"CLEFT PALATE, X-LINKED",C536426,6,1
1,0,203,Epidermolysa bullosa simplex and limb girdle muscular dystrophy,C535955,3,1
1,0,203,Lathosterolosis,C537880,3,1
1,0,203,"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE If",C535744,3,1
1,0,203,Uterine Anomalies,C562565,6,1
1,0,203,"Myopathy, Centronuclear, Autosomal Recessive",C562934,4,1
1,0,203,Juberg-Marsidi syndrome,C537457,3,1
1,0,203,"Mental Retardation, X-Linked 47",C563151,3,1
1,0,203,Pena Shokeir syndrome Type 2,C536646,4,1
1,0,203,Alpha-Methylacyl-CoA Racemase Deficiency,C565768,3,1
1,0,203,"Dental Fluorosis, Acquired",D009050,11,1
1,0,203,"FANCONI ANEMIA, COMPLEMENTATION GROUP J",C563801,3,1
1,0,203,Riddle Syndrome,C567453,3,1
1,0,203,"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ie",C535743,3,1
1,0,203,RETINITIS PIGMENTOSA 2 (disorder),C567523,4,1
1,0,203,Spotted Fever Group Rickettsiosis,D000073605,4,1
1,0,203,Alpha-Thalassemia Myelodysplasia Syndrome,C563023,4,1
1,0,203,"Corneal dystrophy, Lattice type 3",C535480,6,1
1,0,204,Motor Disorders,D000068079,8,1
1,0,204,"RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1",C531651,4,1
1,0,204,Infantile hypophosphatasia,C562646,9,1
1,0,204,"Mental Retardation, X-Linked 30",C563146,4,1
1,0,204,"Bare Lymphocyte Syndrome, Type II, Complementation Group D",C565910,4,1
1,0,204,Endocardial Fibroelastosis,D004695,5,1
1,0,204,Auditory neuropathy,C538268,5,1
1,0,204,Enhanced S-Cone Syndrome,C564835,4,1
1,0,204,"Amyotrophy, monomelic",C538253,6,1
1,0,204,RETINAL CONE DYSTROPHY 1,C566719,4,1
1,0,204,"Cirrhosis, Cryptogenic",C562577,9,1
1,0,204,HHH syndrome,C538380,4,1
1,0,204,Cataract and cardiomyopathy,C538280,5,1
1,0,204,"Mineralocorticoid Excess Syndrome, Apparent",D043204,5,1
1,0,204,"Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1",C563575,4,1
1,0,204,Mastoiditis,D008417,4,1
1,0,204,Pontocerebellar Hypoplasia Type 2,C548070,5,1
1,0,204,Juvenile-Onset Vitelliform Macular Dystrophy,D057826,4,1
1,0,204,"RENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL RECESSIVE",C537758,4,1
1,0,204,"FANCONI ANEMIA, COMPLEMENTATION GROUP N",C563657,4,1
1,0,204,"USHER SYNDROME, TYPE IIA",C536490,5,1
1,0,204,Schwartz-Lelek syndrome,C537519,4,1
1,0,204,11-Beta-hydroxylase deficiency,C535978,4,1
1,0,204,3 beta-Hydroxysteroid dehydrogenase deficiency,C579862,5,1
1,0,204,"Phenylketonuria, Maternal",D017042,5,1
1,0,204,MITOCHONDRIAL NEUROGASTROINTESTINAL ENCEPHALOPATHY SYNDROME,C537477,4,1
1,0,204,"Usher syndrome, type 1B",C536485,4,1
1,0,204,LEBER CONGENITAL AMAUROSIS 12 (disorder),C565697,4,1
1,0,204,Miller Fisher Syndrome,D019846,5,1
1,0,204,DYSTONIA 12,C538001,4,1
1,0,204,"Woolly hair, congenital",C536745,4,1
1,0,204,"Alkalosis, Respiratory",D000472,5,1
1,0,204,Congenital Methemoglobinemia,C580280,4,1
1,0,204,"PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE",C564926,4,1
1,0,204,"CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 2",C535479,5,1
1,0,204,Cortisone reductase deficiency,C536447,4,1
1,0,204,Actinic cheilitis,C535669,4,1
1,0,204,3-Methylglutaconic Aciduria Type IV,C565393,4,1
1,0,204,Arthrogryposis renal dysfunction cholestasis syndrome,C535382,5,1
1,0,204,"Adrenal hyperplasia, congenital, type 5",C538237,4,1
1,0,204,"ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE",C535661,5,1
1,0,204,Monilethrix,D056734,4,1
1,0,204,"Spastic paraplegia 4, autosomal dominant",C536865,6,1
1,0,204,"Hypomagnesemia 1, Intestinal",C566593,5,1
1,0,204,Acidosis,D000138,11,1
1,0,204,Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells,C538539,6,1
1,0,204,"HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 3",C567935,4,1
1,0,204,Arima syndrome,C537430,5,1
1,0,204,Congenital hypoplastic anemia,D029502,4,1
1,0,204,"Alzheimer disease, familial, type 3",C536598,4,1
1,0,204,Genomic Instability,D042822,5,1
1,0,204,Deficiency of galactokinase,D005693,6,1
1,0,204,Retinitis Pigmentosa 17,C563437,4,1
1,0,204,Weaver syndrome,C536687,6,1
1,0,204,"Colorectal cancer, hereditary nonpolyposis, type 1",C535972,4,1
1,0,204,"Spastic paraplegia type 5A, recessive",C536871,5,1
1,0,204,Polyploidy,D011123,4,1
1,0,204,"Hypergonadotropic Ovarian Failure, X-Linked",C567593,7,1
1,0,204,Spastic paraplegia 17,C536644,4,1
1,0,204,Iminoglycinuria,C536285,4,1
1,0,204,15q24 Microdeletion,C579849,5,1
1,0,204,Alcohol-Induced Disorders,D020751,4,1
1,0,204,RETINITIS PIGMENTOSA 3,C564520,7,1
1,0,204,"STRIATONIGRAL DEGENERATION, INFANTILE (disorder)",C537500,5,1
1,0,204,Neuroferritinopathy,C548080,7,1
1,0,204,Blushing,D001821,8,1
1,0,204,delta-Thalassemia,D055538,5,1
1,0,204,Warburg Sjo Fledelius syndrome,C536681,6,1
1,0,204,Megacystis microcolon intestinal hypoperistalsis syndrome,C536138,5,1
1,0,204,Mongolian Spot,D049328,4,1
1,0,204,"Immunodeficiency syndrome, variable",C537362,5,1
1,0,204,Wallerian Degeneration,D014855,4,1
1,0,204,"Multiple Endocrine Neoplasia, Type IV",C567059,4,1
1,0,204,"Spinal Muscular Atrophy, Childhood, Proximal, Autosomal Dominant",C563560,5,1
1,0,204,Bardet-Biedl syndrome 3,C537911,4,1
1,0,204,Alcohol-Related Disorders,D019973,6,1
1,0,204,Li-Fraumeni-Like Syndrome,C567189,4,1
1,0,204,Microglossia,D014060,8,1
1,0,204,"Dystonia 6, torsion (disorder)",C538003,4,1
1,0,204,"Optic Atrophies, Hereditary",D015418,4,1
1,0,204,Obsessions,D009770,8,1
1,0,204,"Parkinsonism-Dystonia, Infantile",C567730,4,1
1,0,204,Stargardt disease 3,C535805,4,1
1,0,204,"Hyperphenylalaninemia, BH4-Deficient, B",C562656,4,1
1,0,204,"CATARACT, NONNUCLEAR POLYMORPHIC CONGENITAL, AUTOSOMAL DOMINANT",C538284,5,1
1,0,204,GLOMUVENOUS MALFORMATIONS,C536827,4,1
1,0,204,Hajdu-Cheney Syndrome,D031845,4,1
1,0,204,Enuresis,D004775,9,1
1,0,204,Neuropathy ataxia and retinis pigmentosa,C537396,4,1
1,0,204,Xerophthalmia,D014985,10,1
1,0,204,Keratitis sicca,C531719,8,1
1,0,204,"Amyotrophic Lateral Sclerosis 4, Juvenile",C566550,6,1
1,0,204,Hay-Wells syndrome,C535847,8,1
1,0,204,Ureteral Calculi,D014514,4,1
1,0,204,DYSTONIA 18 (disorder),C564288,4,1
1,0,204,Aneuploidy,D000782,5,1
1,0,204,ATRIAL SEPTAL DEFECT 1,C566239,5,1
1,0,204,"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1E",C566589,4,1
1,0,204,Gender Dysphoria,D000068116,4,1
1,0,204,HERMANSKY-PUDLAK SYNDROME 2,C537709,5,1
1,0,205,"Xeroderma pigmentosum, group F",C562592,5,1
1,0,205,Cornelia de Lange Syndrome 3,D003635,5,1
1,0,205,SECKEL SYNDROME 2,C537534,5,1
1,0,205,Familial Glucocorticoid Deficiency Type 1,C565974,5,1
1,0,205,Porphobilinogen synthase deficiency,C562618,5,1
1,0,205,"Anemia, Hemolytic, Congenital Nonspherocytic",D000746,5,1
1,0,205,Pontocerebellar Hypoplasia Type 1,C548069,6,1
1,0,205,ATAXIA-TELANGIECTASIA-LIKE DISORDER,C565779,6,1
1,0,205,Warburton Anyane Yeboa syndrome,C536682,5,1
1,0,205,"Opitz-G syndrome, type 2",C538387,9,1
1,0,205,Meconium ileus,D000074270,11,1
1,0,205,Microcolon,C562563,6,1
1,0,205,Intermittent Maple Syrup Urine Disease,D008375,5,1
1,0,205,Histiocytoid Cardiomyopathy,C535584,6,1
1,0,205,SPINAL MUSCULAR ATROPHY WITH RESPIRATORY DISTRESS 1,C536880,5,1
1,0,205,Medullary cystic kidney disease 1,C536137,7,1
1,0,205,Hydranencephaly,D006832,8,1
1,0,205,"Liver Diseases, Parasitic",D008109,9,1
1,0,205,Kaufman-McKusick syndrome,C538159,6,1
1,0,205,"Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency",C565784,5,1
1,0,205,TARP syndrome,C536942,6,1
1,0,205,"DEAFNESS, AUTOSOMAL DOMINANT 1 (disorder)",C565121,10,1
1,0,205,Marek Disease,D008380,7,1
1,0,205,"CARDIOMYOPATHY, DILATED, 1S",C563538,6,1
1,0,205,Cranioectodermal Dysplasia,C562966,8,1
1,0,205,Glucocorticoid-remediable aldosteronism,C563177,7,1
1,0,205,Pseudohypoparathyroidism Type 1B,C548075,7,1
1,0,205,Tyrosinemias,D020176,8,1
1,0,205,Multiple Mitochondrial Dysfunctions Syndrome,C565304,5,1
1,0,205,Congenital disorder of glycosylation type 1A,C535739,7,1
1,0,205,Leri-Weill dyschondrosteosis,C537119,10,1
1,0,205,Perry Syndrome,C566822,9,1
1,0,205,"Short rib-polydactyly syndrome, Verma-Naumoff type",C537602,6,1
1,0,205,Congenital ectopic pupil,C536185,8,1
1,0,205,OROFACIAL CLEFT 1,C566121,7,1
1,0,205,Spastic Paraplegia Type 7,C580457,5,1
1,0,205,MUNGAN SYNDROME,C548078,5,1
1,0,205,Cystinuria type 1,C531664,5,1
1,0,205,Aspartylglucosaminuria,D054880,5,1
1,0,205,"Neural tube defect, folate-sensitive",C536409,8,1
1,0,205,"MYOPATHY, DISTAL 2",C565262,6,1
1,0,205,Hyperamylasemia,D034321,6,1
1,0,205,Endemic goiter,D006043,5,1
1,0,205,Lubs X-linked mental retardation syndrome,C537723,6,1
1,0,205,Adrenal incidentaloma,C538238,5,1
1,0,205,"Uniparental disomy, paternal, chromosome 14",C536471,6,1
1,0,205,Biotinidase Deficiency,D028921,5,1
1,0,205,Hyperphosphatasia with Mental Retardation,C565495,5,1
1,0,205,"Pyloric Stenosis, Hypertrophic",D046248,8,1
1,0,205,Miosis disorder,D015877,10,1
1,0,205,Hot flushes,D019584,6,1
1,0,205,Bile Duct Diseases,D001649,7,1
1,0,205,"EPILEPSY, LATERAL TEMPORAL LOBE, AUTOSOMAL DOMINANT",C537297,7,1
1,0,205,WARFARIN SENSITIVITY (disorder),C567080,5,1
1,0,205,Dubowitz syndrome,C535718,7,1
1,0,205,Torre-Muir syndrome,D055653,5,1
1,0,205,Dysuria,D053159,5,1
1,0,206,MOSAIC VARIEGATED ANEUPLOIDY SYNDROME,C536987,6,1
1,0,206,"Heredodegenerative Disorders, Nervous System",D020271,12,1
1,0,206,Acro-Osteolysis,D030981,13,1
1,0,206,Galloway Mowat syndrome,C537548,7,1
1,0,206,Choline Deficiency,D002796,7,1
1,0,206,Retinitis Pigmentosa 7,C564284,7,1
1,0,206,"SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE 3",C535781,6,1
1,0,206,"Bartter syndrome, type 3",C537653,6,1
1,0,206,Spinal Muscular Atrophies of Childhood,D014897,6,1
1,0,206,Schwannomatosis,C536641,8,1
1,0,206,Coumarin Resistance,C563039,6,1
1,0,206,Mitochondrial Complex II Deficiency,C565375,6,1
1,0,206,Vitamin B 6 Deficiency,D026681,8,1
1,0,206,"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ii",C535747,6,1
1,0,206,Microvillus inclusion disease,C537470,8,1
1,0,206,Primary Hyperoxaluria,D006960,6,1
1,0,206,Hereditary macular coloboma,C535968,8,1
1,0,206,Glucocorticoid deficiency with achalasia,C536008,8,1
1,0,206,Inherited Peripheral Neuropathy,C548028,8,1
1,0,206,Cryptophthalmos syndrome,D058497,6,1
1,0,206,Congenital nystagmus,D020417,9,1
1,0,206,Combined D-2- and L-2-hydroxyglutaric aciduria,C535306,6,1
1,0,206,Sjogren-Larsson Syndrome,D016111,9,1
1,0,206,STOMATOCYTOSIS I,C566111,6,1
1,0,206,Voice Fatigue,D014832,8,1
1,0,206,Hemoglobin M Disease,C581942,6,1
1,0,206,Dysostoses,D004413,10,1
1,0,206,Adrenogenital Syndrome,D047808,6,1
1,0,206,Gonadal dysgenesis XX type deafness,C537286,9,1
1,0,206,Refsum Disease,D012035,6,1
1,0,206,Apparent mineralocorticoid excess,C537422,9,1
1,0,206,Retinitis punctata albescens (disorder),C562733,7,1
1,0,206,"Hyalinosis, Systemic",D057770,9,1
1,0,206,Glucose tolerance test,D005951,10,1
1,0,206,"Syndactyly, type 2",C538153,8,1
1,0,206,Congenital Fibrosis of the Extraocular Muscles,C580012,8,1
1,0,206,Deficiency of acetyl-CoA acetyltransferase,C535434,6,1
1,0,206,Thyroid Dyshormonogenesis 1,C564766,6,1
1,0,206,Respiratory Paralysis,D012133,8,1
1,0,206,Alternating hemiplegia of childhood,C536589,7,1
1,0,206,MASA SYNDROME (disorder),C536029,9,1
1,0,206,Carnitine palmitoyl transferase 2 deficiency,C535589,7,1
1,0,206,"ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, TYPE IIA",C537288,9,1
1,0,206,VATER Association,C536534,10,1
1,0,207,Hypoparathyroidism familial isolated,C537156,7,1
1,0,207,Citrullinemia,D020159,9,1
1,0,207,GALACTOSIALIDOSIS,C536411,11,1
1,0,207,Semantic-Pragmatic Disorder,D007805,10,1
1,0,207,Entropion,D004774,9,1
1,0,207,REM Sleep Behavior Disorder,D020187,9,1
1,0,207,"Porphyria, Erythropoietic",D017092,8,1
1,0,207,Choroid Diseases,D015862,8,1
1,0,207,Frontonasal dysplasia,C538065,7,1
1,0,207,Caroli Disease,D016767,7,1
1,0,207,Tricuspid Valve Stenosis,D014264,15,1
1,0,207,Xerocytosis,C536764,8,1
1,0,207,Thiamine Deficiency,D013832,8,1
1,0,207,OVARIOLEUKODYSTROPHY,C565836,7,1
1,0,207,Variegate Porphyria,D046350,9,1
1,0,207,Giardiasis,D005873,9,1
1,0,207,"FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF",C565577,9,1
1,0,207,Hypochromic anemia,D000747,9,1
1,0,207,Wernicke-Korsakoff Syndrome,D020915,7,1
1,0,207,Alphavirus Infections,D018354,12,1
1,0,207,Chromosomal Instability,D043171,8,1
1,0,207,Delta-Beta Thalassemia,C562716,10,1
1,0,208,Jarcho-Levin syndrome,C537565,9,1
1,0,208,Abruptio Placentae,D000037,8,1
1,0,208,OROFACIODIGITAL SYNDROME VI,C536531,8,1
1,0,208,hypertensive nephropathy,C563161,11,1
1,0,208,Congenital Amaurosis of Retinal Origin,D057130,8,1
1,0,208,Mandibuloacral dysostosis,C535705,11,1
1,0,208,heart rate,D006339,24,1
1,0,208,Male sterility due to Y-chromosome deletions,C536297,8,1
1,0,208,"MYOPATHY, MYOFIBRILLAR, DESMIN-RELATED",C563319,10,1
1,0,208,Gastroparesis,D018589,10,1
1,0,208,Congenital absence of external ear,D065817,8,1
1,0,208,"Hyperbilirubinemia, Hereditary",D006933,8,1
1,0,208,"Jaundice, Chronic Idiopathic",D007566,12,1
1,0,208,"Retinal Dystrophy, Early Onset Severe",C565741,9,1
1,0,208,Pancreatic Cyst,D010181,13,1
1,0,208,Bardet-Biedl syndrome 1 (disorder),C537909,9,1
1,0,208,"Leigh syndrome , French Canadian type",C537004,8,1
1,0,208,"Congenital secretory diarrhea, sodium type (disorder)",C562576,8,1
1,0,208,"Glycogen storage disease, type IX",C580130,9,1
1,0,208,Self-Injurious Behavior,D016728,21,1
1,0,208,Coloboma of optic disc,C535970,14,1
1,0,208,NEPHRONOPHTHISIS 2,C566582,8,1
1,0,208,Hair Diseases,D006201,12,1
1,0,208,"NEPHROLITHIASIS, CALCIUM OXALATE",C563477,14,1
1,0,208,"Spastic paraplegia 10, autosomal dominant",C537482,10,1
1,0,208,"CATARACT, AUTOSOMAL DOMINANT",C565815,8,1
1,0,208,Ellis-Van Creveld Syndrome,D004613,8,1
1,0,209,Congenital pontocerebellar hypoplasia,C580383,15,1
1,0,209,"Usher syndrome, type 1A",D052245,11,1
1,0,209,Primary Progressive Nonfluent Aphasia,D057178,10,1
1,0,209,Dentin Dysplasia,D003805,12,1
1,0,209,"Porphyrias, Hepatic",D017094,9,1
1,0,209,Glycogen Storage Disease Type VII,D006014,11,1
1,0,209,3-Methylglutaconic Aciduria,C579867,12,1
1,0,209,Palmar-plantar erythrodysesthesia syndrome,D060831,11,1
1,0,209,Hartnup Disease,D006250,13,1
1,0,209,Athetosis,D001264,18,1
1,0,209,Hyper-beta-alaninemia,C562684,14,1
1,0,209,Impulsive Behavior,D007175,17,1
1,0,209,Maternally Inherited Leigh Syndrome,C536035,9,1
1,0,209,Lucey-Driscoll syndrome (disorder),C562692,9,1
1,0,209,HOYERAAL-HREIDARSSON SYNDROME,C536068,11,1
1,0,209,Albright's hereditary osteodystrophy,C537045,14,1
1,0,209,Alopecia universalis,C537055,12,1
1,0,209,"Hearing Loss, High-Frequency",D006316,24,1
1,0,209,MITOCHONDRIAL COMPLEX III DEFICIENCY (disorder),C565128,10,1
1,0,210,Carney Triad,C565803,10,1
1,0,210,Multiple Acyl Coenzyme A Dehydrogenase Deficiency,D054069,12,1
1,0,210,RETINITIS PIGMENTOSA 1,C538365,16,1
1,0,210,"Ceroid lipofuscinosis, neuronal 1, infantile",C537948,12,1
1,0,210,Familial Testotoxicosis,C536961,12,1
1,0,210,"Xeroderma pigmentosum, group B",C562590,11,1
1,0,210,Laryngitis,D007827,11,1
1,0,210,Wolcott-Rallison syndrome,C536739,10,1
1,0,210,Polycystic liver disease,C536330,14,1
1,0,210,"Crigler Najjar syndrome, type 2",C536213,10,1
1,0,210,Patella aplasia-hypoplasia,C535568,13,1
1,0,210,Congenital keratoglobus,C562829,16,1
1,0,210,Neurofibrillary degeneration (morphologic abnormality),D016874,15,1
1,0,210,Osteofibrous Dysplasia,C563276,15,1
1,0,210,"Xeroderma pigmentosum, group G",C562593,10,1
1,0,210,Myoglobinuria,D009212,12,1
1,0,210,Dopa-Responsive Dystonia,C538007,15,1
1,0,210,Kernicterus,D007647,11,1
1,0,210,Malignant Hypertension,D006974,12,1
1,0,210,Exudative retinopathy,D058456,12,1
1,0,210,"CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)",C566168,10,1
1,0,211,"Pseudohypoaldosteronism, Type I, Autosomal Dominant",D011546,11,1
1,0,211,Aarskog syndrome,C535331,13,1
1,0,211,"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1",C537308,12,1
1,0,211,Adams Oliver syndrome,C538225,12,1
1,0,211,STARGARDT DISEASE 1 (disorder),C535804,13,1
1,0,211,Laryngomalacia,D055092,19,1
1,0,211,Glucagonoma,D005935,14,1
1,0,211,"Primary hyperoxaluria, type I",C536414,14,1
1,0,211,Hereditary sideroblastic anemia,C536761,13,1
1,0,211,Dental Plaque,D003773,17,1
1,0,211,Hemoglobinuria,D006456,14,1
1,0,211,"Nephronophthisis, familial juvenile",C537699,14,1
1,0,212,Nail-Patella Syndrome,D009261,16,1
1,0,212,Wolfram Syndrome,D014929,14,1
1,0,212,"Congenital, Hereditary, and Neonatal Diseases and Abnormalities",D009358,12,1
1,0,212,Zellweger-Like Syndrome,D015211,12,1
1,0,212,Rubinstein-Taybi Syndrome,D012415,20,1
1,0,212,Vocal Cord Paralysis,D014826,16,1
1,0,212,COENZYME Q10 DEFICIENCY,C564403,13,1
1,0,212,Cholecystitis,D002764,16,1
1,0,212,"Elliptocytosis, Hereditary",D004612,14,1
1,0,212,Exotropia,D005099,29,1
1,0,212,Body Weight,D001835,19,1
1,0,212,Dent's disease,D057973,17,1
1,0,212,Retinal blind spot,D009898,17,1
1,0,212,Trifunctional Protein Deficiency With Myopathy And Neuropathy,C566945,14,1
1,0,212,Methemoglobinemia,D008708,13,1
1,0,212,Sclerocornea,C565209,26,1
1,0,212,Anorectal Malformations,D000071056,20,1
1,0,212,Autosome Abnormalities,D002869,15,1
1,0,212,Hypertensive Retinopathy,D058437,13,1
1,0,212,"AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE (disorder)",C565957,17,1
1,0,212,"HYPERCHOLESTEROLEMIA, AUTOSOMAL RECESSIVE",C566331,15,1
1,0,213,Acute onset pain,D059787,14,1
1,0,213,Pleuropulmonary blastoma,C537516,15,1
1,0,213,Tachypnea,D059246,23,1
1,0,213,Cystinuria,D003555,13,1
1,0,213,Oguchi disease,C537743,15,1
1,0,213,Vitamin B 12 Deficiency,D014806,16,1
1,0,213,Liddle Syndrome,D056929,15,1
1,0,213,MOHR-TRANEBJAERG SYNDROME,C535808,22,1
1,0,213,Ethylmalonic encephalopathy,C535737,15,1
1,0,213,Familial Hyperaldosteronism,C580087,16,1
1,0,213,Inverted Papilloma,D018308,14,1
1,0,214,Saldino-Noonan Syndrome,D012779,14,1
1,0,214,Atrophoderma maculatum,D057088,15,1
1,0,214,Disorders of Porphyrin Metabolism,D011164,17,1
1,0,214,Sinus Tachycardia,D013616,16,1
1,0,214,"Oncocytoma, renal",C537750,20,1
1,0,214,Mouth Diseases,D009059,16,1
1,0,214,"Adenoma, Villous",D018253,15,1
1,0,214,Acth-Independent Macronodular Adrenal Hyperplasia,C565662,18,1
1,0,214,"Spermatogenic Failure, Nonobstructive, Y-Linked",C564030,14,1
1,0,214,Microcytic hypochromic anemia (disorder),C536357,19,1
1,0,214,Taurodontism,C536946,20,1
1,0,214,"Crigler Najjar syndrome, type 1",D003414,14,1
1,0,214,Spastic Ataxia,C564815,22,1
1,0,214,"ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA",C538013,16,1
1,0,215,Occipital Encephalocele,D004677,19,1
1,0,215,Mandibulofacial Dysostosis,D008342,18,1
1,0,215,Mitochondrial encephalopathy,C538525,16,1
1,0,215,Steatorrhea,D045602,23,1
1,0,215,"Necrotizing encephalopathy, infantile subacute, of Leigh",C538590,15,1
1,0,215,"46, XY female",C536769,18,1
1,0,215,HYPERGLYCINURIA (disorder),C563009,15,1
1,0,215,Asthenozoospermia,D053627,28,1
1,0,215,Dysphonia,D055154,30,1
1,0,215,Leigh Syndrome Due To Mitochondrial Complex II Deficiency,C564961,15,1
1,0,215,Leigh Syndrome due to Mitochondrial Complex V Deficiency,C564964,15,1
1,0,215,"Anemia, Megaloblastic",D000749,22,1
1,0,215,Choroideremia,D015794,22,1
1,0,216,Hyperkalemia,D006947,20,1
1,0,216,Leigh Syndrome due to Mitochondrial Complex IV Deficiency,C564963,16,1
1,0,216,Leigh Syndrome due to Mitochondrial Complex III Deficiency,C564962,16,1
1,0,216,Esophageal Stenosis,D004940,19,1
1,0,216,Radioulnar Synostosis,C562408,36,1
1,0,216,"ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, NONDELETION TYPE, X-LINKED",C538258,18,1
1,0,216,"Optic Atrophy, Autosomal Dominant",D029241,23,1
1,0,216,"Heterotaxy, Visceral, 3, Autosomal",C565237,25,1
1,0,216,Renal dysplasia and retinal aplasia (disorder),C537580,17,1
1,0,217,Rothmund-Thomson syndrome,D011038,23,1
1,0,217,Reticulocytosis,D045262,24,1
1,0,217,Cyanosis,D003490,23,1
1,0,218,"46, XY Disorders of Sex Development",D058490,18,1
1,0,218,Sudden death,D003645,20,1
1,0,218,"Xanthomatosis, Cerebrotendinous",D019294,20,1
1,0,218,Aase Smith syndrome 2,C538442,19,1
1,0,218,Infantile Refsum Disease (disorder),D052919,18,1
1,0,219,LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY,C564021,20,1
1,0,219,"Blindness, Cortical",D019575,35,1
1,0,220,Autosomal Recessive Primary Microcephaly,C579935,24,1
1,0,220,Progressive intrahepatic cholestasis (disorder),C535933,26,1
1,0,220,"Hepatic Fibrosis, Congenital",C562378,26,1
1,0,221,Chloracne,D054506,40,1
1,0,221,Hydrophthalmos,D006871,28,1
1,0,221,Ectopic Tissue,D002828,28,1
1,0,221,Gonadoblastoma,D018238,22,1
1,0,221,"Albinism, Ocular",D016117,26,1
1,0,222,Talipes,D000070558,35,1
1,0,222,Sialorrhea,D012798,36,1
1,0,222,Sideroblastic anemia,D000756,27,1
1,0,222,"ALBINOIDISM, OCULOCUTANEOUS, AUTOSOMAL DOMINANT",C566872,27,1
1,0,224,X-Linked Emery-Dreifuss Muscular Dystrophy,D020389,28,1
1,0,224,"Pancreatitis, Alcoholic",D019512,37,1
1,0,224,"DEAFNESS, AUTOSOMAL RECESSIVE (disorder)",C564609,32,1
1,0,224,Birth Weight,D001724,38,1
1,0,224,Esophageal atresia with or without tracheoesophageal fistula,C531835,27,1
1,0,226,Hammer Toe,D037801,33,1
1,0,226,"XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C",C567886,27,1
1,0,226,Pyloric Stenosis,D011707,42,1
1,0,227,X-linked Adrenal Hypoplasia,D000075262,35,1
1,0,227,Hypoplastic Left Heart Syndrome,D018636,35,1
1,0,228,Myofibrillar Myopathy,C580316,36,1
1,0,231,NADH:Q(1) Oxidoreductase deficiency,C537475,31,1
1,0,231,Hypertrichosis,D006983,47,1
1,0,231,Esophageal Atresia,D004933,33,1
1,0,234,"Prostate cancer, familial",C537243,45,1
1,0,234,Oculomotor apraxia,C537423,51,1
1,0,234,Behavioral Symptoms,D001526,43,1
1,0,234,Angelman Syndrome,D017204,46,1
1,0,235,Cone-Rod Dystrophies,D000071700,46,1
1,0,235,Foot Deformities,D005530,44,1
1,0,235,Hereditary Breast and Ovarian Cancer Syndrome,D061325,41,1
1,0,236,Albinism,D000417,44,1
1,0,238,Difficulty walking,D051346,58,1
1,0,239,Potato nose,C538354,73,1
1,0,239,Oligohydramnios,D016104,58,1
1,0,239,Tracheoesophageal Fistula,D014138,45,1
1,0,240,Cytochrome-c Oxidase Deficiency,D030401,43,1
1,0,244,Ciliary Motility Disorders,D002925,57,1
1,0,245,Hermanski-Pudlak Syndrome,D022861,49,1
1,0,247,Hyperopia,D006956,77,1
1,0,247,Nonsyndromic Deafness,C580334,77,1
1,0,249,Familial aplasia of the vermis,C536293,53,1
1,0,251,"Malformations of Cortical Development, Group II",D054081,76,1
1,0,253,Corneal Opacity,D003318,73,1
1,0,255,Muscle Cramp,D009120,80,1
1,0,257,Rhabdomyolysis,D012206,61,1
1,0,257,Familial dilated cardiomyopathy,C536231,69,1
1,0,259,Pachygyria,D054082,85,1
1,0,259,Gait Ataxia,D020234,75,1
1,0,261,Cystic Kidney Diseases,D052177,65,1
1,0,269,Aggressive behavior,D000374,106,1
1,0,277,Congenital ocular coloboma (disorder),D003103,95,1
1,0,282,"Spastic Paraplegia, Hereditary",D015419,98,1
1,0,300,Night Blindness,D009755,118,1
1,0,302,Congenital Disorders of Glycosylation,D018981,116,1
1,0,319,Blindness,D001766,151,1
1,0,330,Conductive hearing loss,D006314,170,1