Disease #01224 (CMH-2 (cardiomyopathy, hypertrophic, familial, type 2 (CMH-2)), OMIM:115195)

Official abbreviation CMH-2
Name cardiomyopathy, hypertrophic, familial, type 2 (CMH-2)
OMIM ID 115195
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 -