Disease #07008 (HYC5 (hydrocephalus, congenital, type 5, susceptibility), OMIM:620241)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curators: Raymond Dalgleish, Gerard Pals, and Dimitra Micha

Official abbreviation	HYC5
Name	hydrocephalus, congenital, type 5, susceptibility
OMIM ID	620241
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SMARCC1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-04-07 10:56:32 +02:00 (CEST)
Date last edited	N/A

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