Disease #02594 (CMD-1L (cardiomyopathy, dilated, type 1L (CMD-1L)), OMIM:606685)

Official abbreviation CMD-1L
Name cardiomyopathy, dilated, type 1L (CMD-1L)
OMIM ID 606685
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene SGCD
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited N/A