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Disease Ontology Browser
hypertrophic cardiomyopathy (DOID:11984)
Alliance: disease page
Synonyms: familial hypertrophic cardiomyopathy; hypertrophic obstructive cardiomyopathy
Alt IDs: DOID:11986, ICD10CM:I42.1, ICD9CM:425.1, ICD9CM:425.11, KEGG:05410, MESH:D002312, MESH:D024741, NCI:C34449, NCI:C84773, OMIM:PS192600, ORDO:155, UMLS_CUI:C0007194, UMLS_CUI:C0949658
Definition: An intrinsic cardiomyopathy that has_material_basis_in autosomal dominant inheritance and that is characterized by abnormal thickening (hypertrophy) of the heart without any obvious cause.

Disease References using Mouse Models (84)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
11/14/2017
MGI 6.11
The Jackson Laboratory