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
C11.270.684.500
C11.768.585.731.813
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:  
blood cerebrospinal fluid
chemically induced classification
congenital complications
diet therapy diagnosis
drug therapy economics
ethnology embryology
enzymology epidemiology
etiology genetics
history immunology
metabolism microbiology
mortality nursing
pathology prevention & control
physiopathology parasitology
psychology radiography
rehabilitation radionuclide imaging
radiotherapy surgery
therapy urine
ultrasonography veterinary
virology  
Record Number:   50480 
Unique Identifier:   D052245 

Occurrence in VHL:
 

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