Phenotype #0000174272
| Individual ID |
00233850 |
| Associated disease |
STGD |
| Phenotype details |
visual acuity now R-20/60 L-20/20; central scotoma (-HP:0000603); no central vision defect; ERG rod-normal/cone-normal |
| Diagnosis/Initial |
Stargardt disease |
| Inheritance |
Familial, autosomal recessive |
| Diagnosis/Definite |
STGD-1 |
| Age/Examination |
46y (46 years) |
| Age/Diagnosis |
29y |
| 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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