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Frasier Syndrome
Hierarchy: | ∟ ∟ ∟ ∟ Frasier Syndrome 9 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Frasier Syndrome 9 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Frasier Syndrome 9 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ |
Broader terms: | |
historyNote*: | 2006; use DENYS-DRASH SYNDROME 2002-2005
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publicMeSHNote*: | 2006; see DENYS-DRASH SYNDROME 2002-2005
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Scope note: | A syndrome characterized by CHRONIC KIDNEY FAILURE and GONADAL DYSGENESIS in phenotypic females with karyotype of 46,XY or 46,XX. It is caused by donor splice-site mutations of Wilms tumor suppressor gene (GENES, WILMS TUMOR) on chromosome 11.
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activeMeSHYear*: | 2007X |
dateCreated*: | 2005-06-30X |
dateEstablished*: | 2006-01-01X |
dateRevised*: | 2006-07-05X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | lktX |
recordOriginator*: | lktX |
Type: | |
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Labels and equivalent concepts: | Frasierin oireyhtymä (fi) XSíndrome de Frasier (es) Frasier-Syndrom (de) syndrom Frasier (cs) |
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