Disease #02786

Official abbreviation CMH-8
Name cardiomyopathy, hypertrophic, familial, type 8 (CMH-8)
OMIM ID 608751
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene MYL3
Associated tissues -
Disease features -
Remarks -