MeSH Browser

MeSH Heading: Cardiomyopathy, Hypertrophic, Familial
Tree Number(s): C14.280.238.100.500; C14.280.484.048.750.070.160.500; C16.320.160
Unique ID: D024741
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D024741
Scope Note: An autosomal dominant inherited form of HYPERTROPHIC CARDIOMYOPATHY. It results from any of more than 50 mutations involving genes encoding contractile proteins such as VENTRICULAR MYOSINS; cardiac TROPONIN T; ALPHA-TROPOMYOSIN.
Entry Term(s): Asymmetric Septal Hypertrophy, Familial; Cardiomyopathy, Familial Hypertrophic; Familial Hypertrophic Cardiomyopathy; Hereditary Ventricular Hypertrophy; Hypertrophic Subaortic Stenosis, Idiopathic; Obstructive Asymmetric Septal Hypertrophy; Ventricular Hypertrophy, Familial; Ventricular Hypertrophy, Hereditary
NLM Classification #: WG 280
Previous Indexing: Cardiomyopathy, Hypertrophic/genetics (1983-2001)
See Also: Tropomyosin; Troponin T; Ventricular Myosins
Public MeSH Note: 2002
History Note: 2002
Date Established: 2002/01/01
Date of Entry: 2001/07/25
Revision Date: 2020/02/28

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

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immunology (IM)

metabolism (ME)

microbiology (MI)

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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, Familial MeSH Descriptor Data 2024