Phenotype #0000054920
Individual ID |
00075145 |
Associated disease |
STGD1 |
Phenotype details |
Stargardt disease; rapid disease progression with central atrophy of the macula and numerous flecks in the midperiphery |
Diagnosis/Initial |
- |
Inheritance |
Unknown |
Diagnosis/Definite |
- |
Age/Examination |
- |
Age/Diagnosis |
- |
Age/Onset |
24y |
Phenotype/Onset |
- |
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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