Bardet-Biedl Syndrome

"Bardet-Biedl Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

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)

Descriptor ID	D020788
MeSH Number(s)	C10.228.140.617.200 C16.131.077.112
Concept/Terms	Bardet-Biedl Syndrome Bardet-Biedl Syndrome Bardet Biedl Syndrome Syndrome, Bardet-Biedl Laurence-Moon-Bardet-Biedl Syndrome Laurence Moon Bardet Biedl Syndrome Syndrome, Laurence-Moon-Bardet-Biedl

Below are MeSH descriptors whose meaning is more general than "Bardet-Biedl Syndrome".

Diseases [C]
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]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Abnormalities, Multiple [C16.131.077]
Bardet-Biedl Syndrome [C16.131.077.112]

Below are MeSH descriptors whose meaning is related to "Bardet-Biedl Syndrome".

Below are MeSH descriptors whose meaning is more specific than "Bardet-Biedl Syndrome".

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