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Porphyria cutanea tarda
Hierarki: | ∟ ∟ ∟ ∟ ∟ Porphyria cutanea tarda 5 sidobegrepp∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Porphyria cutanea tarda 5 sidobegrepp∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Porphyria cutanea tarda 5 sidobegrepp∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Porphyria cutanea tarda 5 sidobegrepp∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Porphyria cutanea tarda 5 sidobegrepp∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Porphyria cutanea tarda 5 sidobegrepp∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Porphyria cutanea tarda 5 sidobegrepp∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Porphyria cutanea tarda 5 sidobegrepp∟ ∟ ∟ ∟ ∟ |
Bredare villkor: | |
Anmärkning: | Porphyria (1966-1992)X |
Anmärkning: | An autosomal dominant or acquired porphyria due to a deficiency of UROPORPHYRINOGEN DECARBOXYLASE in the LIVER. It is characterized by photosensitivity and cutaneous lesions with little or no neurologic symptoms. Type I is the acquired form and is strongly associated with liver diseases and hepatic toxicities caused by alcohol or estrogenic steroids. Type II is the familial form.
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historyNote*: | 95; was PORPHYRIA, CUTANEA TARDA 1993-94
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onlineNote*: | use PORPHYRIA CUTANEA TARDA to search PORPHYRIA, CUTANEA TARDA 1993-94
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publicMeSHNote*: | 95; was PORPHYRIA, CUTANEA TARDA 1993-94
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activeMeSHYear*: | 2007X |
dateCreated*: | 1992-05-22X |
dateEstablished*: | 1993-01-01X |
dateRevised*: | 2006-07-05X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | lktX |
recordOriginator*: | PXPX |
Typ: | |
Samordna villkor: | |
URI: | |
Termer och motsvarande begrepp: | Krooninen porfyria (fi) XPorfyria, krooninen (cutanea tarda) (fi, ersatt) Krooninen ihoporfyria (fi, ersatt) Porphyria cutanea tarda (la-FI, ersatt) |
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