The way property values are displayed:
The way concept relations are shown:
The way concept relations are shown:
Polyendocrinopathies, Autoimmune
Hierarchy: | ∟ ∟ Polyendocrinopathies, Autoimmune 30 coordinate concepts∟ ∟ ∟ Polyendocrinopathies, Autoimmune 30 coordinate conceptsX |
Broader terms: | |
Annotation: | do not coordinate with specific endocrine disease term or CANDIDIASIS unless particularly discussed
X |
History note: | |
historyNote*: | 92
X |
publicMeSHNote*: | 92
X |
Scope note: | 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 |
activeMeSHYear*: | |
dateCreated*: | 1991-05-02X |
dateEstablished*: | 1992-01-01X |
dateRevised*: | 2005-08-02X |
recordAuthorizer*: | agsX |
recordMaintainer*: | agsX |
recordOriginator*: | AGSX |
Type: | |
Coordinate terms: | |
URI: | |
Labels and equivalent concepts: | Autoimmuunipolyendokrinopatiat (fi) XPolyendokrinopatier, autoimmuna (sv) APS I (sv, replaced) APS II (sv, replaced) Autoimmunt polyglandulärt syndrom typ I (sv, replaced) Autoimmunt polyglandulärt syndrom typ II (sv, replaced) Schmidt's Syndrome (en, replaced) Autoimmune Syndrome Type II, Polyglandular (en, replaced) Autoimmune Polyglandular Syndrome Type I (en, replaced) Autoimmune Polyglandular Syndrome Type II (en, replaced) Autoimmune Syndrome Type I, Polyglandular (en, replaced) Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal-Dystrophy (en, replaced) |
Share: |
Loading results...