Table 2.
Target Disease | Associated via Reference Network | Associated via Complemented Network | ||
---|---|---|---|---|
Celiac Disease | Diabetes Mellitus Metabolic Syndrome X Glucose Intolerance Hyperinsulinism Hyperlipidemias |
Calcinosis Dyslipidemias Hyperhomocysteinemia Anemia, Iron-Deficiency Homochromatosis |
Diabetes Mellitus†
Metabolic Syndrome X† Glucose Intolerance† Hyperinsulinism† Congentital Hyperinsulinism** |
Malabsorption Syndromes* Hypoglycemia** Dyslipidemais† Hyperglycemia** Hyperhomocysteinemia† |
Lactose Intolerance | Diabetes Mellitus Metabolic Syndrome X Glucose Intolerance Celiac Disease Dyslipidemias |
Hyperinsulinism Amyotrophic Lateral Sclerosis Insulin Resistance Hyperlipidemias Glucose Metabolism Disorders |
Mucolipidoses* Celiac Disease* Glycogen Storage Disease* Metabolism, Inborn Errors* Malabsorption Syndromes* |
Diabetes Mellitus†
Hypoglycemia** Hyperinsulinism** Glucose Intolerance** Hypokalemia* |
Hypophosphatasia | Metabolic Syndrome X Diabetes Mellitus Glucose Intolerance Metabolic Diseases Dyslipidemias |
Amyotrophic Lateral Sclerosis Diabetes, Gestational Hyperlipidemias Hyperinsulinism Calcinosis |
Acidosis, Renal Tubular* Zellweger Syndrome* Celiac Disease* Peroxisomal Disorders** Refsum Disease* |
Metabolism, Inborn Errors* Adrenoleukodystrophy* Homocystinuria** Diabetes Mellitus† Phenylketonurias* |
Refsum Disease | Zellweger Syndrome Peroxisomal Disorders Chondrodysplasia Punctata, Rhizomelic Adrenoleukodystrophy Homocystinuria |
Porphyrias Protoporphyria, Erythropoietic Hyperhomocysteinemia Diabetic Ketoacidosis Lipid Metabolism, Inborn Errors |
Neuronal Ceroid-Lipofuscinoses* Lipidoses* Peroxisomal Disorders† Zellweger Syndrome† Diabetes Mellitus* |
Leigh Disease* Glycogen Storage Disease* Adrenoleukodystrophy† Malabsorption Syndromes* Glucose Intolerance** |
Fanconi Syndrome |
Hypophosphatemia Glycogen Storage Disease Hypercalcemia Glucose Intolerance Metal Metabolism, Inborn Errors |
Osteomalacia Xanthomatosis, Cerebrotendinous Diabetes Mellitus Calcinosis Metabolic Syndrome X |
Celiac Disease* Glycogen Storage Disease† Diabetes Mellitus† Carbohydrate Metabolism, Inborn Errors* Leigh Disease* |
Diabetes, Gestational* Glucose Intolerance† Hyperinsulinism* Hypoglycemia* Congenital Hyperinsulinism** |
Menkes Kinky Hair Syndrome | N/A | Congenital Disorders of Glycosylation* Hyperglycinemia, Nonketotic* Zellweger Syndrome* Peroxisomal Disorders** Hepatolenticular Degeneration* |
Refsum Disease** Acidosis, Lactic* Albinism* Mitochondrial Myopathies* Adrenoleukodystrophy** |
|
Pyruvate Carboxylase Deficiency Disease |
N/A | Acidosis, Renal Tubular* Carbohydrate Metabolism, Inborn Errors* Hyperglycinemia, Nonketotic* Maple Syrup Urine Disease* Glycogen Storage Disease* |
Amino Acid Metabolism, Inborn Errors* Renal Aminoacidurias** Metabolism, Inborn Errors* Acidosis, Lactic* Pyruvate Metabolism, Inborn Errors* |
|
Rothmund-Thomson Syndrome | N/A | DNA Repair-Deficiency Disorders* Celiac Disease* Metal Metabolism, Inborn Errors** Acidosis* Xanthomatosis, Cerebrotendinous** |
Hypercalcemia* Skin Diseases, Metabolic* Amyloidosis, Familial* Achlorhydria** Osteomalacia** |
|
Sphingolipidoses | N/A | Neuronal Ceroid-Lipofuscinoses* Lipidoses* Carbohydrate Metabolism, Inborn Errors* Diabetes Mellitus* Peroxisomal Disorders* |
Zellweger Syndrome** Glycogen Storage Disease* Adrenoleukodystrophy* Refsum Disease* Glucose Intolerance** |
|
Alkaptonuria | N/A | Carbohydrate Metabolism, Inborn Errors* Glycogen Storage Disease* Zellweger Syndrome* Metabolism, Inborn Errors* Peroxisomal Disorders** |
Amino Acid Metabolism, Inborn Errors* Refsum Disease* Adrenoleukodystrophy** Diabetes Mellitus* Lipid Metabolism, Inborn Errors* |
Notations ‘†’, ‘*’ and ‘**’ are identical to those in Fig. 5