Disease #07100 (CMYO2C (myopathy, congenital, type 2C, severe infantile), OMIM:620278)

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	CMYO2C
Name	myopathy, congenital, type 2C, severe infantile
OMIM ID	620278
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ACTA1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2024-09-05 18:59:46 +02:00 (CEST)
Date last edited	N/A

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