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Hamartomsyndrom, multipelt
Hierarki: | ∟ ∟ ∟ Hamartomsyndrom, multipelt 13 sidobegrepp∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Hamartomsyndrom, multipelt 13 sidobegrepp∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Hamartomsyndrom, multipelt 13 sidobegrepp∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Hamartomsyndrom, multipelt 13 sidobegrepp∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ |
Bredare villkor: | ∟ ∟ ∟ Hamartomsyndrom, multipelt ∟ ∟ ∟ Hamartomsyndrom, multipelt ∟ ∟ ∟ Hamartomsyndrom, multipelt ∟ ∟ ∟ ∟ Hamartomsyndrom, multipelt |
Anmärkning: | |
Anmärkning: | A hereditary disease characterized by multiple ectodermal, mesodermal, and endodermal nevoid and neoplastic anomalies. Papules of the face and oral mucosa are the most characteristic lesion. Other changes occur in the skin, in the thyroid, the breast, the gastrointestinal system, and the nervous system.
X |
Annotation: | do not use /blood supply /chem /second /secret /ultrastruct
X |
historyNote*: | 91(87); was see under NEOPLASMS, MULTIPLE PRIMARY 1987-90
X |
publicMeSHNote*: | 91; was see under NEOPLASMS, MULTIPLE PRIMARY 1987-90
X |
activeMeSHYear*: | |
dateCreated*: | 1986-06-23X |
dateEstablished*: | 1991-01-01X |
dateRevised*: | 2001-07-25X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | nnsX |
recordOriginator*: | VDKX |
Typ: | |
Samordna villkor: | |
URI: | |
Termer och motsvarande begrepp: | Multippeli hamartooma -oireyhtymä (fi) XMultippeli hamartooma -syndrooma (fi, ersatt) Cowdenin tauti (fi, ersatt) Multipelt hamartomsyndrom (sv, ersatt) Hamartoma Syndrome, Multiple (en) Cowden's Disease (en, ersatt) Multiple Hamartoma Syndrome (en, ersatt) Cowden Disease (en, ersatt) Morbus Cowden (la-FI, ersatt) |
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