Phenotype #0000027067
| Individual ID |
00033638 |
| Associated disease |
STGD |
| Phenotype details |
Stargardt disease, severe; severe cone-rod dystrophy; y37, visual acuity OD: 20/400, OS: 20/400. y32: Severe chorioretinal atrophy, macula up to periphery most affected |
| Diagnosis/Initial |
- |
| Inheritance |
Familial, autosomal recessive |
| Diagnosis/Definite |
- |
| Age/Examination |
>07y (later than 7 years) |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Miriam Bauwens |
| Database submission license |
No license selected |
| Created by |
Miriam Bauwens |
| Date created |
2014-10-11 14:12:32 +02:00 (CEST) |
| Date last edited |
2016-07-15 09:36:40 +02:00 (CEST) |
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