Disease #03868 (CMD1KK;CMH22;RCM4 (cardiomyopathy, dilated, type 1KK (CMD-1KK, hypertrophic type 22 (CHM-22), restrictive (RCM-4))), OMIM:615248)

Official abbreviation CMD1KK;CMH22;RCM4
Name cardiomyopathy, dilated, type 1KK (CMD-1KK, hypertrophic type 22 (CHM-22), restrictive (RCM-4))
OMIM ID 615248
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene MYPN
Associated tissues -
Disease features autosomal dominant
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)

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