Disease #01733 (ARCL3A (cutis laxa, autosomal recessive, type IIIA (ARCL-3A, De Barsy syndrome)), OMIM:219150)

Global Variome shared LOVD

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Official abbreviation	ARCL3A
Name	cutis laxa, autosomal recessive, type IIIA (ARCL-3A, De Barsy syndrome)
OMIM ID	219150
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ALDH18A1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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