Phenotype #0000157445
Individual ID |
00208836 |
Associated disease |
LCA2 |
Phenotype details |
20/400 OD, 20/1200 OS, nyctalopia, no nystagmus, flat ERG |
Diagnosis/Initial |
- |
Inheritance |
Familial, autosomal recessive |
Diagnosis/Definite |
- |
Age/Examination |
05y (5 years) |
Age/Diagnosis |
- |
Age/Onset |
00y18m |
Phenotype/Onset |
- |
Protein |
- |
Owner name |
Bailey Glen |
Database submission license |
No license selected |
Created by |
Bailey Glen |
Date created |
2018-12-17 20:22:55 +01:00 (CET) |
Date last edited |
2019-03-03 11:47:38 +01:00 (CET) |
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