Phenotype #0000275808
Individual ID |
00381966 |
Associated disease |
- |
Phenotype details |
visual acuity : od: 0.1, os: 0.1; fundus: subtle oval foveal depression in each eye; color vision: absent; electroretinography: scotopic: normal, 30 hz flicker + photopic: severely abnormal and delayed; photophobia: yes; nystagmus : yes; progression: no |
Diagnosis/Initial |
achromatopsia |
Inheritance |
Familial, autosomal recessive |
Diagnosis/Definite |
- |
Age/Examination |
41y (41 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 |
2021-09-06 15:38:00 +02:00 (CEST) |
Date last edited |
N/A |
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