Disease #06005 (SHPM (myopathy, scapulohumeroperoneal), OMIM:616852)

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	SHPM
Name	myopathy, scapulohumeroperoneal
OMIM ID	616852
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ACTA1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-12-10 23:20:41 +01:00 (CET)
Date last edited	2024-09-05 19:00:31 +02:00 (CEST)

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