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Peutz-Jeghers syndrom
Hierarki: | ∟ ∟ ∟ ∟ ∟ ∟ ∟ Peutz-Jeghers syndrom 12 sidobegrepp∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Peutz-Jeghers syndrom 12 sidobegrepp∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Peutz-Jeghers syndrom 12 sidobegrepp∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Peutz-Jeghers syndrom 12 sidobegrepp∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ |
Bredare villkor: | |
Anmärkning: | A hereditary disease caused by autosomal dominant mutations involving CHROMOSOME 19. It is characterized by the presence of INTESTINAL POLYPS, consistently in the JEJUNUM, and mucocutaneous pigmentation with MELANIN spots of the lips, buccal MUCOSA, and digits.
X |
historyNote*: | 65; was see under POLYPI (now POLYPS) 1963-64
X |
publicMeSHNote*: | 65; was see under POLYPI (now POLYPS) 1963-64
X |
activeMeSHYear*: | |
dateCreated*: | 1999-01-01X |
dateEstablished*: | 1965-01-01X |
dateRevised*: | 2003-07-09X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | lktX |
recordOriginator*: | NLMX |
Typ: | |
Samordna villkor: | |
URI: | |
Termer och motsvarande begrepp: | Peutz-Jeghersin oireyhtymä (fi) XPeutz-Jeghersin syndrooma (fi, ersatt) Peutz-Jeghersin polypoosi (fi, ersatt) Peutz-Jeghers Syndrome (en) Polyps-and-Spots Syndrome (en, ersatt) Peutz-Jegher's Syndrome (en, ersatt) Polyposis, Hamartomatous Intestinal (en, ersatt) Lentiginosis, Perioral (en, ersatt) Syndroma Peutz-Jeghers (la-FI, ersatt) |
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