Search on: BARDET-BIEDL SYNDROME 
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Descriptor English:   Bardet-Biedl Syndrome 
Descriptor Spanish:   Síndrome de Bardet-Biedl 
Descriptor Portuguese:   Síndrome de Bardet-Biedl 
Synonyms English:   Laurence-Moon-Bardet-Biedl Syndrome  
Tree Number:   C10.228.140.617.200
C16.131.077.112
Definition English:   An autosomal recessive disorder characterized by RETINITIS PIGMENTOSA; POLYDACTYLY; OBESITY; MENTAL RETARDATION; hypogenitalism; renal dysplasia; and short stature. This syndrome has been distinguished as a separate entity from LAURENCE-MOON SYNDROME. (From J Med Genet 1997 Feb;34(2):92-8) 
Indexing Annotation English:   note entry term: do not confuse with LAURENCE-MOON SYNDROME
See Related English:   Intellectual Disability
 
History Note English:   2000 
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:   34282 
Unique Identifier:   D020788 

Occurrence in VHL:
 

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