Disease #00473 (OCA-1A (albinism, oculocutaneous, type IA (OCA-1A)), OMIM:203100)

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Official abbreviation	OCA-1A
Name	albinism, oculocutaneous, type IA (OCA-1A)
OMIM ID	203100
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TYR
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-07-24 21:36:02 +02:00 (CEST)
Date last edited	N/A