Disease #03291 (CMH-13 (cardiomyopathy, hypertrophic, familial, type 13 (CMH-13)), OMIM:613243)

Official abbreviation CMH-13
Name cardiomyopathy, hypertrophic, familial, type 13 (CMH-13)
OMIM ID 613243
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene TNNC1
Associated tissues -
Disease features -
Remarks -