Phenotype #0000056540
| Individual ID |
00076765 |
| Associated disease |
STGD1 |
| Phenotype details |
Stargardt disease; y30: Visual acuity OD 20/60 OS 20/50, atrophy in the macula in both eyes, normal ERG |
| Diagnosis/Initial |
- |
| Inheritance |
Unknown |
| Diagnosis/Definite |
- |
| Age/Examination |
- |
| Age/Diagnosis |
- |
| Age/Onset |
25y |
| Phenotype/Onset |
visual symptoms or of first ophthalmic consultation where a diagnosis of Stargardt disease |
| Protein |
- |
| Owner name |
Stéphanie Cornelis |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Stéphanie Cornelis |
| Date created |
2016-02-22 12:22:09 +01:00 (CET) |
| Date last edited |
N/A |
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