Search on: USHER SYNDROMES 
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Descriptor English:   Usher Syndromes 
Descriptor Spanish:   Síndromes de Usher 
Descriptor Portuguese:   Síndromes de Usher 
Tree Number:   C09.218.458.341.186.500.500
C09.218.458.341.887.886
C10.597.751.418.341.186.500.500
C10.597.751.418.341.887.886
C10.597.751.941.162.625.500
C11.768.585.658.500.813
C11.966.075.375.500
C16.131.077.299.500
C16.320.290.684.500
C23.888.592.763.393.341.887.886
Definition English:   Autosomal recessive hereditary disorders characterized by congenital SENSORINEURAL HEARING LOSS and RETINITIS PIGMENTOSA. Genetically and symptomatically heterogeneous, clinical classes include type I, type II, and type III. Their severity, age of onset of retinitis pigmentosa and the degree of vestibular dysfunction are variable. 
History Note English:   2006 
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:   50480 
Unique Identifier:   D052245 

Occurrence in VHL:
 

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