Structured Summary
Abstract
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)
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Synonyms
5 entry terms
- Laurence-Moon-Bardet-Biedl Syndrome
- Bardet Biedl Syndrome
- Laurence Moon Bardet Biedl Syndrome
- Syndrome, Bardet-Biedl
- Syndrome, Laurence-Moon-Bardet-Biedl
MeSH Record
Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
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Indexing Annotation
note entry term: do not confuse with LAURENCE-MOON SYNDROME
MeSH Record
History Note
2000
MeSH Record
Previous Indexing
- Bardet-Biedl Syndrome (1966-1999)
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AMA Style
References
- National Library of Medicine. Bardet-Biedl Syndrome. Medical Subject Headings (MeSH). 2026. Unique ID D020788. http://id.nlm.nih.gov/mesh/2026/D020788
- Bardet-Biedl Syndrome. In: Wikipedia. https://en.wikipedia.org/wiki/Bardet%E2%80%93Biedl_syndrome
- Bardet-Biedl Syndrome. In: Wikidata. https://www.wikidata.org/wiki/Q1678281