Disease #06877 (DFNA (deafness, nonsyndromic (DFNA, autosomal dominant)))
| Official abbreviation |
DFNA |
| Name |
deafness, nonsyndromic (DFNA, autosomal dominant) |
| OMIM ID |
- |
| Inheritance |
- |
| Individuals reported having this disease |
20 |
| Phenotype entries for this disease |
8 |
| Associated with 6 genes |
GREB1L, MYO6, MYO7A, REST, TECTA, TMC1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-12-10 23:20:41 +01:00 (CET) |
| Date last edited |
N/A |
Individuals
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