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CARDIOMYOPATHY, HYPERTROPHIC, FAMILIAL
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DeCS
Descriptor
English
:
Cardiomyopathy, Hypertrophic, Familial
Descriptor
Spanish
:
Cardiomiopatía Hipertrófica Familiar
Descriptor
Portuguese
:
Cardiomiopatia Hipertrófica Familiar
Synonyms
English
:
Familial Hypertrophic Cardiomyopathy
Tree Number:
C14.280.238.100.500
C14.280.484.150.070.160.500
C16.320.160
Definition
English
:
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.
See Related
English
:
Tropomyosin
Troponin T
Ventricular Myosins
History Note
English
:
2002
Allowable Qualifiers
English
:
BL
blood
CF
cerebrospinal fluid
CI
chemically induced
CL
classification
CO
complications
DI
diagnosis
DH
diet therapy
DT
drug therapy
EC
economics
EM
embryology
EN
enzymology
EP
epidemiology
EH
ethnology
ET
etiology
GE
genetics
HI
history
IM
immunology
ME
metabolism
MI
microbiology
MO
mortality
NU
nursing
PS
parasitology
PA
pathology
PP
physiopathology
PC
prevention & control
PX
psychology
RA
radiography
RI
radionuclide imaging
RT
radiotherapy
RH
rehabilitation
SU
surgery
TH
therapy
US
ultrasonography
UR
urine
VE
veterinary
VI
virology
Record Number:
36019
Unique Identifier:
D024741
Occurrence in VHL
:
Similar:
DeCS
CID-10
SciELO
LILACS
LIS