Phenotype #0000350872
| Individual ID |
00465320 |
| Associated disease |
USH1F |
| Phenotype details |
congenital bilateral hearing loss and first began to experience night blindness when the proband was about 10 years old |
| Diagnosis/Initial |
USH |
| Inheritance |
Familial, autosomal recessive |
| Diagnosis/Definite |
USH1F |
| Age/Examination |
26y (26 years) |
| Age/Diagnosis |
26y |
| Age/Onset |
congenital |
| Phenotype/Onset |
congenital |
| Protein |
We |
| Owner name |
Yanbao Xiang |
| Database submission license |
No license selected |
| Created by |
Yanbao Xiang |
| Date created |
2025-05-13 10:12:45 +02:00 (CEST) |
| Date last edited |
2025-05-14 09:27:40 +02:00 (CEST) |
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