Disease #07032 (VSCM2 (myopathy, visceral, type 2), OMIM:619350)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
Register as submitter | Log in

	Curator: Global Variome, with Curator vacancy

Official abbreviation	VSCM2
Name	myopathy, visceral, type 2
OMIM ID	619350
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MYH11
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-10-03 16:57:42 +02:00 (CEST)
Date last edited	N/A

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.