| | Disease Ontology | MeSH |
| Disease ID: | DOID:11984 | D002312 |
| Disease Name: | hypertrophic cardiomyopathy | Cardiomyopathy, Hypertrophic |
| Category: | Disease Ontology | MeSH |
| Type: | | Cardiovascular Diseases |
| Define: | An intrinsic cardiomyopathy that is characterized by abnormal thickening (hypertrophy) of the heart without any obvious cause. | A form of CARDIAC MUSCLE disease, characterized by left and/or right ventricular hypertrophy (HYPERTROPHY, LEFT VENTRICULAR; HYPERTROPHY, RIGHT VENTRICULAR), frequent asymmetrical involvement of the HEART SEPTUM, and normal or reduced left ventricular volume. Risk factors include HYPERTENSION; AORTIC STENOSIS; and gene MUTATION; (FAMILIAL HYPERTROPHIC CARDIOMYOPATHY). |
| Alias: | hypertrophic obstructive cardiomyopathy | Cardiomyopathy, Hypertrophic//Cardiomyopathies, Hypertrophic//Hypertrophic Cardiomyopathies//Hypertrophic Cardiomyopathy//Cardiomyopathy, Hypertrophic Obstructive//Cardiomyopathies, Hypertrophic Obstructive//Hypertrophic Obstructive Cardiomyopathies//Hypertrophic Obstructive Cardiomyopathy//Obstructive Cardiomyopathies, Hypertrophic//Obstructive Cardiomyopathy, Hypertrophic |
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