Phenotype #0000295598
| Individual ID |
00402837 |
| Associated disease |
- |
| Phenotype details |
lesions, right eye/left eye: single, vitelliruptive lesion/vitelliruptive lesion, visual acuity: right eye, left eye: 20/100, 20/63, color vision: errors, visual field: relative scotoma, electro-oculogram right eye/left eye: 149/141 |
| Diagnosis/Initial |
- |
| Inheritance |
Familial, autosomal dominant |
| Diagnosis/Definite |
dystrophy, macular, vitelliform type 2 (VMD2) |
| Age/Examination |
56y5m (56 years, 5 months) |
| Age/Diagnosis |
- |
| Age/Onset |
21y |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
LOVD |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Anna Tracewska |
| Date created |
2022-02-11 14:52:14 +01:00 (CET) |
| Date last edited |
N/A |
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