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Crigler-Najjar Syndrome
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historyNote*: | 91(75); was see under HYPERBILIRUBINEMIA, HEREDITARY 1975-90
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onlineNote*: | use HYPERBILIRUBINEMIA, HEREDITARY to search CRIGLER-NAJJAR SYNDROME 1966-74
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publicMeSHNote*: | 91; was see under HYPERBILIRUBINEMIA, HEREDITARY 1975-90
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Scope note: | A familial form of congenital hyperbilirubinemia transmitted as an autosomal recessive trait. It is characterized by icterus and brain damage caused by a glucuronyl transferase deficiency in the liver and faulty bilirubin conjugation.
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activeMeSHYear*: | 2007X |
dateCreated*: | 1999-01-01X |
dateEstablished*: | 1991-01-01X |
dateRevised*: | 2006-07-05X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | lktX |
recordOriginator*: | NLMX |
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Labels and equivalent concepts: | Crigler-Najjarin oireyhtymä (fi) XCrigler-Najjarin syndrooma (fi, replaced) Crigler-Najjars syndrom (sv) Crigler-Najar Syndrome (en, replaced) Syndroma Crigler-Najjar (la-FI, replaced) |
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