Search Ontology:
Human Disease

familial hypertrophic cardiomyopathy

Term ID
DOID:0080326
Synonyms
Definition
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. https://ghr.nlm.nih.gov/condition/familial-hypertrophic-cardiomyopathy#genes
References
Ontology
Human Disease   ( DOID:0080326 )
Relationships
is a type of
has subtype
Other Pages
Genes Involved
Zebrafish Models