| Descriptor English: | Polyendocrinopathies, Autoimmune | ||||||
| Descriptor Spanish: |
Poliendocrinopatías Autoinmunes
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| Descriptor Portuguese: | Poliendocrinopatias Autoimunes | ||||||
| Descriptor French: | Polyendocrinopathies auto-immunes | ||||||
| Entry term(s): |
AIRE Deficiencies AIRE Deficiency APECED 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 |
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| Tree number(s): |
C19.787 C20.111.750 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D016884 | ||||||
| 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. |
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| Annotation: | do not coordinate with specific endocrine disease term or CANDIDIASIS unless particularly discussed |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CN congenital CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Previous Indexing: |
Autoimmune Diseases (1968-1991) Endocrine Diseases (1978-1991) |
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| Public MeSH Note: | 1992 |
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| History Note: | 1992 |
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| DeCS ID: | 29879 | ||||||
| Unique ID: | D016884 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1992/01/01 | ||||||
| Date of Entry: | 1991/05/02 | ||||||
| Revision Date: | 2013/07/08 |
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Polyendocrinopathies, Autoimmune
- Preferred
Polyglandular Type III Autoimmune Syndrome
- Narrower
Polyglandular Type I Autoimmune Syndrome
- Narrower
Polyglandular Type II Autoimmune Syndrome
- Narrower
| Concept UI |
M0025689 |
| 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. |
| Preferred term | Polyendocrinopathies, Autoimmune |
| Entry term(s) |
Autoimmune Polyendocrinopathy Polyendocrinopathy, Autoimmune |
| Concept UI |
M0552088 |
| Preferred term | Polyglandular Type III Autoimmune Syndrome |
| Entry term(s) |
Autoimmune Polyglandular Syndrome Type III Autoimmune Polyglandular Syndrome, Type 3 Autoimmune Syndrome Type III, Polyglandular Polyglandular Autoimmune Syndrome, Type 3 |
| Concept UI |
M0025691 |
| Preferred term | Polyglandular Type I Autoimmune Syndrome |
| Entry term(s) |
AIRE Deficiencies AIRE Deficiency APECED APS Type 1 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 1 Autoimmune Polyglandular Syndrome, Type I Autoimmune Syndrome Type I, Polyglandular Deficiency, AIRE Polyendocrinopathy Candidiasis Ectodermal Dystrophy, Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy, Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal-Dystrophy, Autoimmune Polyglandular Autoimmune Syndrome, Type 1 Polyglandular Autoimmune Syndrome, Type I |
| Concept UI |
M0025692 |
| Preferred term | Polyglandular Type II Autoimmune Syndrome |
| Entry term(s) |
Autoimmune Polyendocrine Syndrome, Type 2 Autoimmune Polyendocrine Syndrome, Type II Autoimmune Polyglandular Syndrome Type II Autoimmune Syndrome Type II, Polyglandular Diabetes Mellitus, Addison Disease, Myxedema Diabetes Mellitus, Addison's Disease, Myxedema Multiple Endocrine Deficiency Syndrome, Type 2 Polyendocrine Autoimmune Syndrome, Type II Polyglandular Autoimmune Syndrome, Type 2 Polyglandular Deficiency Syndrome, Type 2 Schmidt Syndrome Schmidt's Syndrome Syndrome, Schmidt Syndrome, Schmidt's |
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