Disease #04611 (PMGYCHA (polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis (PMGYCHA)), OMIM:616531)

Official abbreviation	PMGYCHA
Name	polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis (PMGYCHA)
OMIM ID	616531
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PI4KA
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-09-23 10:25:23 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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Global Variome shared LOVD