Table 7.
Putative Associated Diseases for the NIPA2 Gene.
| Number | MalaCards ID | Name of Associated Diseases | MIFTS | Solr Relevance Score |
|---|---|---|---|---|
| 1 | PD006 | Prader–Willi Syndrome | 60 | 5.045 |
| 2 | CHL002 | Childhood Absence Epilepsy | 60 | 4.53 |
| 3 | ANG001 | Angelman Syndrome | 65 | 4.495 |
| 4 | CHL058 | Childhood Electroclinical Syndrome | 21 | 3.568 |
| 5 | ATS013 | Autosomal Recessive Congenital Ichthyosis | 65 | 2.523 |
| 6 | SCH015 | Schizophrenia | 76 | 0.215 |
| 7 | ATS364 | Autism | 68 | 0.196 |
| 8 | EPL164 | Epilepsy | 73 | 0.124 |
| 9 | HYP595 | Hypertension, Essential | 87 | 0.088 |
| 10 | OST002 | Osteoporosis | 79 | 0.088 |
| 11 | BDY004 | Body Mass Index Quantitative Trait Locus 11 | 78 | 0.088 |
| 12 | DWN001 | Down Syndrome | 70 | 0.088 |
| 13 | ATS007 | Autism Spectrum Disorder | 69 | 0.088 |
| 14 | THR014 | Thrombocytopenia | 67 | 0.088 |
| 15 | MCR010 | Microcephaly | 56 | 0.088 |
| 16 | BNM029 | Bone Mineral Density Quantitative Trait Locus 15 | 51 | 0.088 |
| 17 | HYD064 | Hydrocephalus, Congenital, 1 | 47 | 0.088 |
| 18 | BNM022 | Bone Mineral Density Quantitative Trait Locus 8 | 43 | 0.088 |
| 19 | CHR523 | Chromosome 15q11.2 Deletion Syndrome | 31 | 0.088 |
| 20 | IMM162 | Immunoglobulin E Concentration, Serum | 29 | 0.088 |
MalaCards InFormaTion Score (MIFTS)-annotation strength (max 100). Source: MalaCards: HGMD, OMIM, ClinVar, GTR, Orphanet, DISEASES, Novoseek, GeneCards, and MalaCards.