| DISEASE NAME | Benign familial hematuria |
| DISEASE CATEGORY (ICD10) | Congenital malformations, deformations and chromosomal abnormalities |
| DISEASE ID (ICD10) | Q87.8 |
| DISEASE ID (OMIM) | 104200; 203780; 301050 |
| 5 combinations linked to 97562 | OLI133; OLI318; OLI319; OLI504; OLI916 |
| 4 gene combinations linked to 97562 | COL4A3; COL4A4; COL4A6; COL4A3; COL4A5; COL4A3; COL4A4; COL4A5; LAMA5 |
| ORPHANET ID | 97562 |