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Bardet-Biedl Syndrome
MeSH Descriptor Data 2024
Details
Qualifiers
MeSH Tree Structures
Concepts
MeSH Heading
Bardet-Biedl Syndrome
Tree Number(s)
C10.228.140.617.200
C11.270.684.624
C16.131.077.245.125
C16.320.184.125
Unique ID
D020788
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D020788
Annotation
note entry term: do not confuse with
LAURENCE-MOON SYNDROME
Scope Note
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)
Entry Term(s)
Laurence-Moon-Bardet-Biedl Syndrome
Previous Indexing
Bardet-Biedl Syndrome (1966-1999)
See Also
Intellectual Disability
Public MeSH Note
2000
History Note
2000
Date Established
2000/01/01
Date of Entry
1999/11/08
Revision Date
2018/06/15
Allowable Qualifiers
blood (BL)
cerebrospinal fluid (CF)
chemically induced (CI)
classification (CL)
complications (CO)
diagnosis (DI)
diagnostic imaging (DG)
diet therapy (DH)
drug therapy (DT)
economics (EC)
embryology (EM)
enzymology (EN)
epidemiology (EP)
ethnology (EH)
etiology (ET)
genetics (GE)
history (HI)
immunology (IM)
metabolism (ME)
microbiology (MI)
mortality (MO)
nursing (NU)
parasitology (PS)
pathology (PA)
physiopathology (PP)
prevention & control (PC)
psychology (PX)
radiotherapy (RT)
rehabilitation (RH)
surgery (SU)
therapy (TH)
urine (UR)
veterinary (VE)
virology (VI)
Nervous System Diseases [C10]
Central Nervous System Diseases [C10.228]
Brain Diseases [C10.228.140]
Hypothalamic Diseases [C10.228.140.617]
Bardet-Biedl Syndrome [C10.228.140.617.200]
Hypothalamic Neoplasms [C10.228.140.617.477]
Laurence-Moon Syndrome [C10.228.140.617.500]
Pituitary Diseases [C10.228.140.617.738]
Eye Diseases [C11]
Eye Diseases, Hereditary [C11.270]
Retinitis Pigmentosa [C11.270.684]
Alstrom Syndrome [C11.270.684.249]
Bardet-Biedl Syndrome [C11.270.684.624]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Abnormalities, Multiple [C16.131.077]
Ciliopathies [C16.131.077.245]
Alstrom Syndrome [C16.131.077.245.063]
Bardet-Biedl Syndrome [C16.131.077.245.125]
Caroli Disease [C16.131.077.245.250]
Ciliary Motility Disorders [C16.131.077.245.500]
von Hippel-Lindau Disease [C16.131.077.245.750]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Ciliopathies [C16.320.184]
Alstrom Syndrome [C16.320.184.063]
Bardet-Biedl Syndrome [C16.320.184.125]
Caroli Disease [C16.320.184.250]
Ciliary Motility Disorders [C16.320.184.500]
Polycystic Kidney Diseases [C16.320.184.625]
von Hippel-Lindau Disease [C16.320.184.750]
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Bardet-Biedl Syndrome
Preferred
Concept UI
M0328149
Scope Note
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)
Terms
Bardet-Biedl Syndrome
Preferred Term
Term UI
T358149
Date
10/12/1999
LexicalTag
EPO
ThesaurusID
Laurence-Moon-Bardet-Biedl Syndrome
Term UI
T366093
Date
10/12/1999
LexicalTag
EPO
ThesaurusID
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