Disease #03477 (CMH18 (cardiomyopathy, hypertrophic, familial, type 18 (CMH-18)), OMIM:613874)

Official abbreviation CMH18
Name cardiomyopathy, hypertrophic, familial, type 18 (CMH-18)
OMIM ID 613874
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene PLN
Associated tissues -
Disease features -
Remarks -

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