* We recommend a score >= 0.08 for meaningful Gene-Disease associations
| GeneID | Gene_Symbol | DisGeNet_diseaseID | Disease_name | DisGeNet_sourceDB | |
| 5372 | PMM1 | C0019189 | Hepatitis, Chronic | 0.00273291246481375 | LHGDN |
| 5372 | PMM1 | C0027612 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities | 0.00273291246481375 | LHGDN |
| 5372 | PMM1 | C0349653 | Congenital disorder of glycosylation type 1A | 0.0008241803526393 | BEFREE |