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) |
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