Search on: CARDIOMYOPATHY, HYPERTROPHIC, FAMILIAL 
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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:
 

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