Disease #00474 (OCA-1B (albinism, oculocutaneous, type IB (OCA-1B)), OMIM:606952)

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	Curator: Johan T. den Dunnen

Official abbreviation	OCA-1B
Name	albinism, oculocutaneous, type IB (OCA-1B)
OMIM ID	606952
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 21:37:14 +02:00 (CEST)
Date last edited	N/A