Disease #04585 (MSMB (myopathy, myosin storage, autosomal recessive (MSMB)), OMIM:255160)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	MSMB
Name	myopathy, myosin storage, autosomal recessive (MSMB)
OMIM ID	255160
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MYH7
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-09-23 10:25:23 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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