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
|