Disease #02319 (CMH-6 (cardiomyopathy, hypertrophic, familial, type 6 (CMH-6)), OMIM:600858)

Official abbreviation CMH-6
Name cardiomyopathy, hypertrophic, familial, type 6 (CMH-6)
OMIM ID 600858
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene PRKAG2
Associated tissues -
Disease features -
Remarks -