Disease #05756 (CNM6 (myopathy, centronuclear, type 6, with fiber-type disproportion (CNM6)), OMIM:617760)

Global Variome shared LOVD

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

Official abbreviation	CNM6
Name	myopathy, centronuclear, type 6, with fiber-type disproportion (CNM6)
OMIM ID	617760
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MAP3K20
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-05-25 13:38:36 +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.