Phenotype #0000054434
Individual ID |
00016878 |
Associated disease |
STGD1 |
Phenotype details |
Stargardt disease; Visual acuity: OD 10/100-1, OS 10/60-1, parafoveal or perifoveal flecks with frequent atrophy of the central macula. |
Diagnosis/Initial |
- |
Inheritance |
Unknown |
Diagnosis/Definite |
- |
Age/Examination |
- |
Age/Diagnosis |
- |
Age/Onset |
- |
Phenotype/Onset |
- |
Protein |
- |
Owner name |
Stéphanie Cornelis |
Database submission license |
No license selected |
Created by |
Johan den Dunnen |
Date created |
2016-07-15 13:11:40 +02:00 (CEST) |
Date last edited |
N/A |
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