Phenotype #0000310973
Individual ID |
00419693 |
Associated disease |
- |
Phenotype details |
- |
Diagnosis/Initial |
Stargardt disease |
Inheritance |
Familial, autosomal dominant |
Diagnosis/Definite |
- |
Age/Examination |
- |
Age/Diagnosis |
- |
Age/Onset |
- |
Phenotype/Onset |
- |
Protein |
- |
Owner name |
Rebekkah Hitti-Malin |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2022-10-21 12:50:15 +02:00 (CEST) |
Date last edited |
N/A |
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