Disease #03137 (RCM-3 (cardiomyopathy, restrictive, familial, type 3 (RCM-3)), OMIM:612422)

Official abbreviation RCM-3
Name cardiomyopathy, restrictive, familial, type 3 (RCM-3)
OMIM ID 612422
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene TNNT2
Associated tissues -
Disease features -
Remarks -