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Nervous System Diseases > Central Nervous System Diseases > Brain Diseases > Hypothalamic Diseases > Bardet-Biedl Syndrome
... > Eye Diseases > Retinal Diseases > Retinal Degeneration > Retinal Dystrophies > Retinitis Pigmentosa > Bardet-Biedl Syndrome
... > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Eye Diseases, Hereditary > Retinal Degeneration > Retinal Dystrophies > Retinitis Pigmentosa > Bardet-Biedl Syndrome
... > Eye Diseases > Eye Diseases, Hereditary > Retinal Degeneration > Retinal Dystrophies > Retinitis Pigmentosa > Bardet-Biedl Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Ciliopathies > Bardet-Biedl Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Abnormalities, Multiple > Ciliopathies > Bardet-Biedl Syndrome

Preferred term

Bardet-Biedl Syndrome  

Type

  • Topical Descriptor

Broader concept

Related concepts

Entry terms

  • Laurence Moon Bardet Biedl Syndrome
  • Laurence-Moon-Bardet-Biedl Syndrome
  • Syndrome, Laurence-Moon-Bardet-Biedl

Note

  • 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)

History note

  • 2000

In other languages

  • Bardet-Biedlin oireyhtymä

    Finnish

  • Bardet-Biedl
  • Bardet-Biedlin syndrooma
  • Lawrence-Moon-Bardet-Biedl
  • Lawrence-Moon-Bardet-Biedl'n oireyhtymä
  • Lawrence-Moon-Bardet-Biedl'n syndrooma
  • syndroma Bardet-Biedl
  • Bardet-Biedls syndrom

    Swedish

  • Laurence-Moon-Bardet-Biedls syndrom

URI

http://www.yso.fi/onto/mesh/D020788

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