Phenotype #0000174253
Individual ID |
00233821 |
Associated disease |
STGD |
Phenotype details |
visual acuity now R-20/200 L-20/50; central scotoma (HP:0000603); severe central vision defect; ERG rod-dec/cone-normal |
Diagnosis/Initial |
Stargardt disease |
Inheritance |
Familial, autosomal recessive |
Diagnosis/Definite |
STGD-1 |
Age/Examination |
62y (62 years) |
Age/Diagnosis |
39y |
Age/Onset |
- |
Phenotype/Onset |
- |
Protein |
- |
Owner name |
Terry-Lynn Young |
Database submission license |
No license selected |
Created by |
Jim Houston |
Date created |
2019-03-20 11:55:21 +01:00 (CET) |
Date last edited |
N/A |
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