Disease #03728 (CNM-4 (myopathy, centronuclear, type 4 (CNM-4)), OMIM:614807)

Official abbreviation CNM-4
Name myopathy, centronuclear, type 4 (CNM-4)
OMIM ID 614807
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene CCDC78
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited N/A