| DISEASE NAME | Non-syndromic genetic deafness |
| DISEASE CATEGORY (ICD10) | Diseases of the ear and mastoid process |
| DISEASE ID (ICD10) | H90.5 |
| DISEASE ID (OMIM) | N.A. |
| 15 combinations linked to 87884 | OLI013; OLI060; OLI135; OLI136; OLI192; OLI193; OLI194; OLI251; OLI252; OLI254; OLI406; OLI454; OLI497; OLI831; OLI1649 |
| 8 gene combinations linked to 87884 | GJB2; MITF; GJB2; GJB3; GJB2; TMPRSS3; PCDH15; USH1G; ADGRV1; USH1G; ATP2B2; CDH23; ADGRV1; PDZD7; GFI1; MYO6 |
| ORPHANET ID | 87884 |