Phenotype #0000054335
| Individual ID |
00074538 |
| Associated disease |
OCA1A |
| Phenotype details |
Generalized hypopigmentation (HP:0007513) |
| Diagnosis/Initial |
- |
| Inheritance |
Familial, autosomal recessive |
| Diagnosis/Definite |
- |
| Age/Examination |
35y (35 years) |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Pieter Klap |
| Database submission license |
No license selected |
| Created by |
Pieter Klap |
| Date created |
2016-07-08 10:08:48 +02:00 (CEST) |
| Date last edited |
2016-10-11 12:31:54 +02:00 (CEST) |
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