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Congenital Hypothyroidism
Hierarchy: | ∟ ∟ ∟ ∟ Congenital Hypothyroidism 11 coordinate concepts∟ ∟ ∟ Congenital Hypothyroidism 11 coordinate concepts∟ ∟ ∟ ∟ Congenital Hypothyroidism 11 coordinate concepts∟ ∟ ∟ ∟ ∟ Congenital Hypothyroidism 11 coordinate concepts∟ ∟ ∟ ∟ Congenital Hypothyroidism 11 coordinate conceptsX |
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historyNote*: | 2006 (1966)
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publicMeSHNote*: | 2006; see CRETINISM 1966-2005
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Scope note: | A condition in infancy or early childhood due to an in-utero deficiency of THYROID HORMONES that can be caused by genetic or environmental factors, such as thyroid dysgenesis or HYPOTHYROIDISM in infants of mothers treated with THIOURACIL during pregnancy. Endemic cretinism is the result of iodine deficiency. Clinical symptoms include severe MENTAL RETARDATION, impaired skeletal development, short stature, and MYXEDEMA.
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activeMeSHYear*: | |
dateCreated*: | 1999-01-01X |
dateRevised*: | 2005-08-02X |
recordAuthorizer*: | agsX |
recordMaintainer*: | agsX |
recordOriginator*: | NLMX |
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Labels and equivalent concepts: | Kretinismi (fi) XSynnynnäinen kilpirauhasen vajaatoiminta (fi, replaced) Synnynnäinen hypotyreoosi (fi, replaced) Kongenitaalinen hypotyreoosi (fi, replaced) Kretinism (sv) Cretinism (en, replaced) Cretinismus (la-FI, replaced) |
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