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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