Disease #05807 (ARCL2C (cutis laxa, autosomal recessive, type IIC (ARCL2C)), OMIM:617402)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	ARCL2C
Name	cutis laxa, autosomal recessive, type IIC (ARCL2C)
OMIM ID	617402
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ATP6V1E1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-08-08 20:56:19 +02:00 (CEST)
Date last edited	N/A

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