Phenotype #0000128226
Individual ID |
00163089 |
Associated disease |
DFNA |
Phenotype details |
- |
Diagnosis/Initial |
deafness, nonsyndromic (DFNA) |
Inheritance |
Familial, autosomal dominant |
Diagnosis/Definite |
DFNA-22 |
Age/Examination |
- |
Age/Diagnosis |
- |
Age/Onset |
- |
Phenotype/Onset |
- |
Protein |
- |
Owner name |
Anne-Françoise Roux |
|
|