| DISEASE NAME | Alport syndrome |
| DISEASE CATEGORY (ICD10) | Congenital malformations, deformations and chromosomal abnormalities |
| DISEASE ID (ICD10) | Q87.8 |
| DISEASE ID (OMIM) | 104200; 203780; 301050 |
| 35 combinations linked to 63 | OLI033; OLI034; OLI133; OLI154; OLI155; OLI156; OLI157; OLI318; OLI376; OLI377; OLI378; OLI379; OLI380; OLI381; OLI382; OLI383; OLI384; OLI385; OLI386; OLI387; OLI388; OLI516; OLI971; OLI972; OLI973; OLI974; OLI975; OLI1373; OLI1374; OLI1375; OLI1644; OLI1645; OLI1646; OLI1647; OLI1648 |
| 4 gene combinations linked to 63 | COL4A3; COL4A4; COL4A6; COL4A3; COL4A5; COL4A4; COL4A5; COL4A3; COL4A4 |
| ORPHANET ID | 63 |