Disease #05474 (MFM8 (myopathy, myofibrillar, type 8 (MFM-8)), OMIM:617258)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	MFM8
Name	myopathy, myofibrillar, type 8 (MFM-8)
OMIM ID	617258
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PYROXD1
Associated tissues	-
Disease features	autosomal recessive
Remarks	-
Date created	2018-10-19 06:30:51 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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