Disease #05641 (HELIX (HELIX syndrome (HELIX)), OMIM:617671)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Official abbreviation	HELIX
Name	HELIX syndrome (HELIX)
OMIM ID	617671
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CLDN10
Associated tissues	-
Disease features	-
Remarks	autosomal recessive
Date created	2019-08-01 13:02:23 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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