Disease #00850 (OCA7 (albinism, oculocutaneous, type VII (OCA7)), OMIM:615179)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	OCA7
Name	albinism, oculocutaneous, type VII (OCA7)
OMIM ID	615179
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	C10orf11
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2020-08-27 12:00:26 +02:00 (CEST)

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