MeSH Browser

MeSH Heading: Cardiomyopathy, Hypertrophic
Tree Number(s): C14.280.238.100; C14.280.484.048.750.070.160
Unique ID: D002312
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D002312
Annotation: do not confuse with CARDIAC HYPERTROPHY see CARDIOMEGALY
Scope Note: 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).
Entry Version: SUBVALV STENOSIS
Entry Term(s): Cardiomyopathy, Hypertrophic Obstructive
NLM Classification #: WG 280
Public MeSH Note: 86; was IDIOPATHIC HYPERTROPHIC SUBVALVULAR STENOSIS 1966-85
Online Note: use CARDIOMYOPATHY, HYPERTROPHIC to search IDIOPATHIC HYPERTROPHIC SUBVALVULAR STENOSIS 1966-85
History Note: 86; was IDIOPATHIC HYPERTROPHIC SUBVALVULAR STENOSIS 1966-85
Date Established: 1966/01/01
Date of Entry: 1999/01/01
Revision Date: 2020/02/28

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

congenital (CN)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Cardiomyopathy, Hypertrophic MeSH Descriptor Data 2025