Disease #07100 (CMYO2C (myopathy, congenital, type 2C, severe infantile), OMIM:620278)

Global Variome shared LOVD

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

	Curator: Marc Ferre

Official abbreviation	CMYO2C
Name	myopathy, congenital, type 2C, severe infantile
OMIM ID	620278
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	2024-09-05 18:59:46 +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.