| DISEASE NAME | Rare genetic deafness |
| DISEASE CATEGORY (ICD10) | None |
| DISEASE ID (ICD10) | N.A. |
| DISEASE ID (OMIM) | N.A. |
| 12 combinations linked to 96210 | OLI1100; OLI1101; OLI1102; OLI1103; OLI1104; OLI1313; OLI1314; OLI1315; OLI1316; OLI1317; OLI1318; OLI1319 |
| 11 gene combinations linked to 96210 | CDH23; GJB2; KCNQ4; MPDZ; SLC26A4; GJB2; KCNQ4; MPDZ; CDH23; MPDZ; SLC26A4; CDH23; GJB2; MPDZ; SLC26A4; CDH23; GJB2; MPDZ; GJB2; SLC4A11; EYA1; GJB2; GJB2; OTOA; GJB2; GSDME; GJB2; OTOA; OTOF; PJVK; ADGRV1; USH2A |
| ORPHANET ID | 96210 |