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Descriptor English: Cardiomyopathy, Hypertrophic, Familial
Descriptor Spanish: Cardiomiopatía Hipertrófica Familiar
Descriptor Portuguese: Cardiomiopatia Hipertrófica Familiar
Descriptor French: Cardiomyopathie hypertrophique familiale
Entry term(s): Asymmetric Septal Hypertrophy, Familial
Cardiomyopathies, Familial Hypertrophic
Cardiomyopathy, Familial Hypertrophic
Familial Hypertrophic Cardiomyopathies
Familial Hypertrophic Cardiomyopathy
Familial Ventricular Hypertrophies
Familial Ventricular Hypertrophy
Hereditary Ventricular Hypertrophies
Hereditary Ventricular Hypertrophy
Hypertrophic Cardiomyopathies, Familial
Hypertrophic Cardiomyopathy, Familial
Hypertrophic Subaortic Stenosis, Idiopathic
Hypertrophies, Hereditary Ventricular
Hypertrophy, Familial Ventricular
Hypertrophy, Hereditary Ventricular
Obstructive Asymmetric Septal Hypertrophy
Ventricular Hypertrophies, Familial
Ventricular Hypertrophies, Hereditary
Ventricular Hypertrophy, Familial
Ventricular Hypertrophy, Hereditary
Tree number(s): C14.280.238.100.500
C14.280.484.048.750.070.160.500
C16.320.160
RDF Unique Identifier: https://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.
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
Previous Indexing: Cardiomyopathy, Hypertrophic/genetics (1983-2001)
Public MeSH Note: 2002
History Note: 2002
Related: Tropomyosin MeSH
Troponin T MeSH
Ventricular Myosins MeSH
DeCS ID: 36019
Unique ID: D024741
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 2002/01/01
Date of Entry: 2001/07/25
Revision Date: 2013/07/08
Cardiomyopathy, Hypertrophic, Familial - Preferred
Concept UI M0371730
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.
Preferred term Cardiomyopathy, Hypertrophic, Familial
Entry term(s) Asymmetric Septal Hypertrophy, Familial
Cardiomyopathies, Familial Hypertrophic
Cardiomyopathy, Familial Hypertrophic
Familial Hypertrophic Cardiomyopathies
Familial Hypertrophic Cardiomyopathy
Familial Ventricular Hypertrophies
Familial Ventricular Hypertrophy
Hereditary Ventricular Hypertrophies
Hereditary Ventricular Hypertrophy
Hypertrophic Cardiomyopathies, Familial
Hypertrophic Cardiomyopathy, Familial
Hypertrophies, Hereditary Ventricular
Hypertrophy, Familial Ventricular
Hypertrophy, Hereditary Ventricular
Ventricular Hypertrophies, Familial
Ventricular Hypertrophies, Hereditary
Ventricular Hypertrophy, Familial
Ventricular Hypertrophy, Hereditary
Obstructive Asymmetric Septal Hypertrophy - Related but not broader or narrower
Concept UI M0579499
Preferred term Obstructive Asymmetric Septal Hypertrophy
Hypertrophic Subaortic Stenosis, Idiopathic - Related but not broader or narrower
Concept UI M0579500
Preferred term Hypertrophic Subaortic Stenosis, Idiopathic



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