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Sjogren-Larsson Syndrome
Hierarchy: | ∟ ∟ ∟ ∟ ∟ Sjogren-Larsson Syndrome 26 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ Sjogren-Larsson Syndrome 26 coordinate concepts∟ ∟ ∟ ∟ Sjogren-Larsson Syndrome 26 coordinate concepts∟ ∟ ∟ ∟ Sjogren-Larsson Syndrome 26 coordinate concepts∟ ∟ ∟ ∟ ∟ Sjogren-Larsson Syndrome 26 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ Sjogren-Larsson Syndrome 26 coordinate concepts∟ ∟ ∟ ∟ ∟ Sjogren-Larsson Syndrome 26 coordinate concepts∟ ∟ ∟ ∟ ∟ Sjogren-Larsson Syndrome 26 coordinate concepts∟ ∟ ∟ ∟ Sjogren-Larsson Syndrome 26 coordinate conceptsX |
Broader terms: | ∟ ∟ ∟ ∟ ∟ Sjogren-Larsson Syndrome ∟ ∟ ∟ ∟ ∟ ∟ Sjogren-Larsson Syndrome ∟ ∟ ∟ ∟ Sjogren-Larsson Syndrome ∟ ∟ ∟ ∟ Sjogren-Larsson Syndrome ∟ ∟ ∟ ∟ ∟ Sjogren-Larsson Syndrome ∟ ∟ ∟ ∟ ∟ ∟ Sjogren-Larsson Syndrome ∟ ∟ ∟ ∟ ∟ Sjogren-Larsson Syndrome ∟ ∟ ∟ ∟ ∟ Sjogren-Larsson Syndrome ∟ ∟ ∟ ∟ Sjogren-Larsson Syndrome |
Annotation: | do not confuse with SJOGREN'S SYNDROME; in titles & translations use diacritic: Sjögren-Larsson
X |
History note: | Ichthyosis (1966-1990)X |
historyNote*: | 91; was see ICHTHYOSIS 1984-90
X |
onlineNote*: | search ICHTHYOSIS 1984-90
X |
publicMeSHNote*: | 91; was see ICHTHYOSIS 1984-90
X |
Scope note: | An autosomal recessive neurocutaneous disorder characterized by severe ichthyosis MENTAL RETARDATION; SPASTIC PARAPLEGIA; and congenital ICHTHYOSIS. It is caused by mutation of gene encoding microsomal fatty ALDEHYDE DEHYDROGENASE leading to defect in fatty alcohol metabolism.
X |
activeMeSHYear*: | 2007X |
dateCreated*: | 1990-06-06X |
dateEstablished*: | 1991-01-01X |
dateRevised*: | 2006-07-05X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | lktX |
recordOriginator*: | AGSX |
Type: | |
Coordinate terms: | |
URI: | |
Labels and equivalent concepts: | Sjögren-Larssonin oireyhtymä (fi) XFatty Aldehyde Dehydrogenase Deficiency Disease (en, replaced) Síndrome de Sjögren-Larsson (es) σύνδρομο Sjogren-Larsson (el) Sjögren-Larsson-Syndrom (de) Sjoegrenův-Larssonův syndrom (cs) |
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