Disease #02787

Official abbreviation CMH-10
Name cardiomyopathy, hypertrophic, familial, type 10 (CMH-10)
OMIM ID 608758
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene MYL2
Associated tissues -
Disease features -
Remarks -