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DO Term : familial hypertrophic cardiomyopathy [DOID:0080326] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A hypertrophic cardiomyopathy that is characterized by thickening of the heart muscle and has_material_basis_in autosomal dominant inheritance of one or more gene mutations.

synonyms:
UMLS_CUI:C0949658,
MESH:D024741,
ORDO:217569,
NCI:C84773,
SNOMEDCT_US_2023_03_01:83978005,
PS192600,
OMIM:PS192600

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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