Phenotype #0000281759
Individual ID |
00388166 |
Associated disease |
- |
Phenotype details |
Nystagmus: Wandering eye movement, best corrected visual acuity right eye/left eye: UCSM/UCSM, fundus: Macular coloboma like degeneration, ERG: Extinguished |
Diagnosis/Initial |
Leber congenital amaurosis |
Inheritance |
Unknown |
Diagnosis/Definite |
Leber congenital amaurosis |
Age/Examination |
6m |
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 |
2021-11-02 11:59:44 +01:00 (CET) |
Date last edited |
N/A |
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