Disease #07099 (CMYO2B (myopathy, congenital, type 2B, severe infantile), OMIM:620265)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	CMYO2B
Name	myopathy, congenital, type 2B, severe infantile
OMIM ID	620265
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
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 18:58:31 +02:00 (CEST)
Date last edited	N/A

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