Polyendocrinopathies, Autoimmune


AIRE Deficiencies

AIRE Deficiency


APS Type 1

Autoimmune Polyendocrine Syndrome, Type 2

Autoimmune Polyendocrine Syndrome, Type II

Autoimmune Polyendocrinopathy

Autoimmune Polyendocrinopathy Candidiasis Ectodermal Dystrophy

Autoimmune Polyendocrinopathy Syndrome Type 1

Autoimmune Polyendocrinopathy with Candidiasis and Ectodermal Dystrophy

Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy

Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal-Dystrophy

Autoimmune Polyglandular Syndrome Type I

Autoimmune Polyglandular Syndrome Type II

Autoimmune Polyglandular Syndrome Type III

Autoimmune Polyglandular Syndrome, Type 1

Autoimmune Polyglandular Syndrome, Type 3

Autoimmune Polyglandular Syndrome, Type I

Autoimmune Syndrome Type I, Polyglandular

Autoimmune Syndrome Type II, Polyglandular

Autoimmune Syndrome Type III, Polyglandular

Deficiency, AIRE

Diabetes Mellitus, Addison Disease, Myxedema

Diabetes Mellitus, Addison's Disease, Myxedema

Multiple Endocrine Deficiency Syndrome, Type 2

Polyendocrine Autoimmune Syndrome, Type II

Polyendocrinopathy Candidiasis Ectodermal Dystrophy, Autoimmune

Polyendocrinopathy, Autoimmune

Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy, Autoimmune

Polyendocrinopathy-Candidiasis-Ectodermal-Dystrophy, Autoimmune

Polyglandular Autoimmune Syndrome, Type 1

Polyglandular Autoimmune Syndrome, Type 2

Polyglandular Autoimmune Syndrome, Type 3

Polyglandular Autoimmune Syndrome, Type I

Polyglandular Deficiency Syndrome, Type 2

Polyglandular Type I Autoimmune Syndrome

Polyglandular Type II Autoimmune Syndrome

Polyglandular Type III Autoimmune Syndrome

Schmidt Syndrome

Schmidt's Syndrome

Syndrome, Schmidt

Syndrome, Schmidt's

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.