Phenotype #0000157446
| Individual ID |
00208837 |
| Associated disease |
- |
| Phenotype details |
20/60 OD, 20/70 OS, nyctalopia, no nystagmus, bony spicules, flat ERG |
| Diagnosis/Initial |
Early onset retinal dystrophy |
| Inheritance |
Familial, autosomal recessive |
| Diagnosis/Definite |
- |
| Age/Examination |
15y (15 years) |
| Age/Diagnosis |
- |
| Age/Onset |
00y18m |
| Phenotype/Onset |
- |
| Protein |
WBaileyGlen |
| Owner name |
Bailey Glen |
| Database submission license |
No license selected |
| Created by |
Bailey Glen |
| Date created |
2018-12-17 20:25:33 +01:00 (CET) |
| Date last edited |
2019-03-03 11:47:38 +01:00 (CET) |
|