Phenotype #0000157642

Individual ID 00209036
Associated disease OCA
Diagnosis/Initial oculocutaneous albinism
Diagnosis/Definite OCA-1A
Phenotype details Oculocutaneous albinism
Inheritance Familial, autosomal recessive
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2018-12-22 15:10:51 +01:00 (CET)
Date last edited N/A

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