Visningssätt för begreppens/termernas förhållanden:
Det sätt begreppsrelationer visas:
Det sätt begreppsrelationer visas:
Polyendokrinopatier, autoimmuna
Hierarki: | ∟ ∟ Polyendokrinopatier, autoimmuna 30 sidobegrepp∟ ∟ ∟ Polyendokrinopatier, autoimmuna 30 sidobegreppX |
Bredare villkor: | |
Anmärkning: | |
Anmärkning: | Autoimmune diseases affecting multiple endocrine organs. Type I is characterized by childhood onset and chronic mucocutaneous candidiasis (CANDIDIASIS, CHRONIC MUCOCUTANEOUS), while type II exhibits any combination of adrenal insufficiency (ADDISON'S DISEASE), lymphocytic thyroiditis (THYROIDITIS, AUTOIMMUNE;), HYPOPARATHYROIDISM; and gonadal failure. In both types organ-specific ANTIBODIES against a variety of ENDOCRINE GLANDS have been detected. The type II syndrome differs from type I in that it is associated with HLA-A1 and B8 haplotypes, onset is usually in adulthood, and candidiasis is not present.
X |
Annotation: | do not coordinate with specific endocrine disease term or CANDIDIASIS unless particularly discussed
X |
historyNote*: | 92
X |
publicMeSHNote*: | 92
X |
activeMeSHYear*: | |
dateCreated*: | 1991-05-02X |
dateEstablished*: | 1992-01-01X |
dateRevised*: | 2005-08-02X |
recordAuthorizer*: | agsX |
recordMaintainer*: | agsX |
recordOriginator*: | AGSX |
Typ: | |
Samordna villkor: | |
URI: | |
Termer och motsvarande begrepp: | Autoimmuunipolyendokrinopatiat (fi) XAPS I (sv, ersatt) APS II (sv, ersatt) Autoimmunt polyglandulärt syndrom typ I (sv, ersatt) Autoimmunt polyglandulärt syndrom typ II (sv, ersatt) Polyendocrinopathies, Autoimmune (en) Schmidt's Syndrome (en, ersatt) Autoimmune Syndrome Type II, Polyglandular (en, ersatt) Autoimmune Polyglandular Syndrome Type I (en, ersatt) Autoimmune Polyglandular Syndrome Type II (en, ersatt) Autoimmune Syndrome Type I, Polyglandular (en, ersatt) Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal-Dystrophy (en, ersatt) |
Dela: |
Laddar resultat...