Disease #05864 (MYOFTA (myopathy, congenital, with fast-twitch (type II) fiber atrophy (MYOFTA)), OMIM:618414)

Global Variome shared LOVD

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Official abbreviation	MYOFTA
Name	myopathy, congenital, with fast-twitch (type II) fiber atrophy (MYOFTA)
OMIM ID	618414
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MYL1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-10-27 09:59:32 +01:00 (CET)
Date last edited	N/A

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