Disease #02766 (CMD-1O (cardiomyopathy, dilated, type 1O (CMD-1O)), OMIM:608569)

Official abbreviation CMD-1O
Name cardiomyopathy, dilated, type 1O (CMD-1O)
OMIM ID 608569
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene ABCC9
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited N/A

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