Disease #07119 (CMYO22B (myopathy, congenital, type 22B), OMIM:620369)

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	CMYO22B
Name	myopathy, congenital, type 22B
OMIM ID	620369
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SCN4A
Associated tissues	-
Disease features	-
Remarks	-
Date created	2024-11-11 21:47:23 +01:00 (CET)
Date last edited	N/A

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