DeCS

Descriptor English:

Cardiomyopathy, Hypertrophic, Familial

Descriptor Spanish:

Cardiomiopatía Hipertrófica Familiar

Spanish from Spain

Descriptor	miocardiopatía hipertrófica familiar
Scope note:	Forma hereditaria autosómica dominante de MIOCARDIOPATÍalt-0141A HIPERTRÓFICA. Es consecuencia de cualquiera de más de 50 mutaciones que afectan a los genes que codifican las proteínas contráctiles, como las MIOSINAS VENTRICULARES, TROPONINA T cardíaca, TROPOMIOSINA ALFA.

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

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

Concept UI	M0579499
Preferred term	Obstructive Asymmetric Septal Hypertrophy

Concept UI	M0579500
Preferred term	Hypertrophic Subaortic Stenosis, Idiopathic

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