Phenotype #0000056270
Individual ID |
00076495 |
Associated disease |
STGD1 |
Phenotype details |
Stargardt disease; moderate central fundus changes, visual acuity: OD 1,6/10, OS 1,6/10 |
Diagnosis/Initial |
- |
Inheritance |
Unknown |
Diagnosis/Definite |
- |
Age/Examination |
- |
Age/Diagnosis |
- |
Age/Onset |
6y |
Phenotype/Onset |
unknown |
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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