Disease #07258 (CMYO10B (myopathy, congenital, type 10B, mild variant), OMIM:620249)

Global Variome shared LOVD

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Official abbreviation	CMYO10B
Name	myopathy, congenital, type 10B, mild variant
OMIM ID	620249
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MEGF10
Associated tissues	-
Disease features	-
Remarks	-
Date created	2026-04-10 22:29:38 +02:00 (CEST)
Date last edited	2026-04-10 22:32:21 +02:00 (CEST)

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