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Bardet-Biedl Syndrome
Hierarchy: | ∟ ∟ ∟ ∟ Bardet-Biedl Syndrome 34 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Bardet-Biedl Syndrome 34 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ |
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Annotation: | note X ref: do not confuse with LAURENCE-MOON-BARDET-BIEDL SYNDROME see BARDET-BIEDL SYNDROME
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History note: | Bardet-Biedl Syndrome (1966-1999)X |
historyNote*: | 2000
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publicMeSHNote*: | 2000
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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)
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activeMeSHYear*: | |
dateCreated*: | 1999-11-08X |
dateEstablished*: | 2000-01-01X |
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Labels and equivalent concepts: | Bardet-Biedlin oireyhtymä (fi) XLawrence-Moon-Bardet-Biedl’n syndrooma (fi, replaced) Lawrence-Moon-Bardet-Biedl’n oireyhtymä (fi, replaced) Bardet-Biedlin syndrooma (fi, replaced) Bardet-Biedls syndrom (sv) Laurence-Moon-Bardet-Biedls syndrom (sv, replaced) Laurence-Moon-Bardet-Biedl Syndrome (en, replaced) Syndroma Bardet-Biedl (la-FI, replaced) |
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