Disease #01734 (ARCL-2A (cutis laxa, autosomal recessive, type IIA (ARCL-2A)), OMIM:219200)

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	Curator: Johan T. den Dunnen

Official abbreviation	ARCL-2A
Name	cutis laxa, autosomal recessive, type IIA (ARCL-2A)
OMIM ID	219200
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ATP6V0A2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A