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Laurence-Moon Syndrome
Hierarchy: | ∟ ∟ ∟ ∟ Laurence-Moon Syndrome 34 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Laurence-Moon 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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historyNote*: | 2000 (1966)
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publicMeSHNote*: | 2000; see LAURENCE-MOON-BIEDL SYNDROME 1966-1999
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Scope note: | An autosomal recessive condition characterized by hypogonadism; spinocerebellar degeneration; MENTAL RETARDATION; RETINITIS PIGMENTOSA; and OBESITY. This syndrome was previously referred to as Laurence-Moon-Biedl syndrome until BARDET-BIEDL SYNDROME was identified as a distinct entity. (From N Engl J Med. 1989 Oct 12;321(15):1002-9)
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activeMeSHYear*: | |
dateCreated*: | 1999-01-01X |
dateRevised*: | 1999-11-03X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | KEVX |
recordOriginator*: | NLMX |
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Labels and equivalent concepts: | Laurence-Moonin oireyhtymä (fi) XLaurence-Moon-Biedl Syndrome (en, replaced) Síndrome de Laurence-Moon (es) σύνδρομο Laurence-Moon-Biedl (el) Laurence-Moon-Syndrom (de) Laurenceův-Moonův syndrom (cs) Síndrome de Laurence-Moon-Biedl (es, replaced) Laurence-Moon-Biedl-Syndrom (de, replaced) |
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