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
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- MESH:D024741
- MIM:PS192600
- NCI:C84773
- ORDO:217569
- SNOMEDCT_US_2023_03_01:83978005
- UMLS_CUI:C0949658
- Ontology
- Human Disease ( DOID:0080326 )
- is a type of
-
- has subtype
Other Pages
Genes Involved
Zebrafish Models