Phenotype #0000306391
| Individual ID |
00414592 |
| Associated disease |
- |
| Phenotype details |
refractive error: myopia; best corrected visual acuity: 0.3; full field electroretinography, flicker: amplitude: 65, implicit time: 32.5; mixed amplitude: a-wave: 149, b-wave: 89; rod response: absent |
| Diagnosis/Initial |
- |
| Inheritance |
Familial, autosomal recessive |
| Diagnosis/Definite |
congenital stationary night blindness |
| Age/Examination |
45y (45 years) |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
LOVD |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Anna Tracewska |
| Date created |
2022-07-29 12:13:59 +02:00 (CEST) |
| Date last edited |
N/A |
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