Phenotype #0000242972
Individual ID |
00324430 |
Associated disease |
OCA1 |
Phenotype details |
Subclinical nystagmus, Grade 1 foveal hypoplasia, |
Diagnosis/Initial |
Albinism |
Inheritance |
Familial, autosomal recessive |
Diagnosis/Definite |
Albinism |
Age/Examination |
05y (5 years) |
Age/Diagnosis |
05y |
Age/Onset |
- |
Phenotype/Onset |
- |
Protein |
- |
Owner name |
Mervyn Thomas |
Database submission license |
No license selected |
Created by |
Mervyn Thomas |
Date created |
2020-12-12 11:25:16 +01:00 (CET) |
Date last edited |
2020-12-13 10:46:27 +01:00 (CET) |
|