Disease #07250 (CMYO25 (myopathy, congenital, type 25), OMIM:620964)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	CMYO25
Name	myopathy, congenital, type 25
OMIM ID	620964
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	JPH1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2026-03-30 15:27:20 +02:00 (CEST)
Date last edited	N/A

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