Disease #05787 (MFM7 (myopathy, myofibrillar, type 7 (MFM7)), OMIM:617114)

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	MFM7
Name	myopathy, myofibrillar, type 7 (MFM7)
OMIM ID	617114
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	KY
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-07-14 18:35:23 +02:00 (CEST)
Date last edited	N/A

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