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Medical Subject Headings
| Preferred Name | Polyendocrinopathies, Autoimmune | |
| Synonyms |
Autoimmune Syndrome Type I, Polyglandular Polyendocrinopathy-Candidiasis-Ectodermal-Dystrophy, Autoimmune Multiple Endocrine Deficiency Syndrome, Type 2 Autoimmune Polyendocrinopathy Polyglandular Autoimmune Syndrome, Type 1 AIRE Deficiencies Polyglandular Autoimmune Syndrome, Type 2 Autoimmune Polyendocrine Syndrome, Type II Autoimmune Polyendocrine Syndrome, Type 2 Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy, Autoimmune Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal-Dystrophy Polyglandular Type I Autoimmune Syndrome Autoimmune Polyglandular Syndrome, Type I Autoimmune Polyendocrinopathy Candidiasis Ectodermal Dystrophy Polyglandular Type III Autoimmune Syndrome Autoimmune Polyglandular Syndrome Type I Autoimmune Polyglandular Syndrome Type III Polyendocrine Autoimmune Syndrome, Type II Schmidt Syndrome Polyglandular Autoimmune Syndrome, Type 3 Autoimmune Polyendocrinopathy with Candidiasis and Ectodermal Dystrophy Polyglandular Deficiency Syndrome, Type 2 Autoimmune Polyglandular Syndrome Type II Autoimmune Syndrome Type III, Polyglandular Diabetes Mellitus, Addison's Disease, Myxedema Polyendocrinopathy, Autoimmune Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy APECED Autoimmune Polyendocrinopathy Syndrome Type 1 AIRE Deficiency APS Type 1 Polyglandular Autoimmune Syndrome, Type I Polyendocrinopathy Candidiasis Ectodermal Dystrophy, Autoimmune Autoimmune Polyglandular Syndrome, Type 3 Deficiency, AIRE Syndrome, Schmidt's Autoimmune Polyglandular Syndrome, Type 1 Polyglandular Type II Autoimmune Syndrome Autoimmune Syndrome Type II, Polyglandular Diabetes Mellitus, Addison Disease, Myxedema Syndrome, Schmidt Schmidt's Syndrome |
|
| Definitions |
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. |
|
| ID |
http://purl.bioontology.org/ontology/MESH/D016884 |
|
| altLabel |
Autoimmune Syndrome Type I, Polyglandular Polyendocrinopathy-Candidiasis-Ectodermal-Dystrophy, Autoimmune Multiple Endocrine Deficiency Syndrome, Type 2 Autoimmune Polyendocrinopathy Polyglandular Autoimmune Syndrome, Type 1 AIRE Deficiencies Polyglandular Autoimmune Syndrome, Type 2 Autoimmune Polyendocrine Syndrome, Type II Autoimmune Polyendocrine Syndrome, Type 2 Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy, Autoimmune Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal-Dystrophy Polyglandular Type I Autoimmune Syndrome Autoimmune Polyglandular Syndrome, Type I Autoimmune Polyendocrinopathy Candidiasis Ectodermal Dystrophy Polyglandular Type III Autoimmune Syndrome Autoimmune Polyglandular Syndrome Type I Autoimmune Polyglandular Syndrome Type III Polyendocrine Autoimmune Syndrome, Type II Schmidt Syndrome Polyglandular Autoimmune Syndrome, Type 3 Autoimmune Polyendocrinopathy with Candidiasis and Ectodermal Dystrophy Polyglandular Deficiency Syndrome, Type 2 Autoimmune Polyglandular Syndrome Type II Autoimmune Syndrome Type III, Polyglandular Diabetes Mellitus, Addison's Disease, Myxedema Polyendocrinopathy, Autoimmune Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy APECED Autoimmune Polyendocrinopathy Syndrome Type 1 AIRE Deficiency APS Type 1 Polyglandular Autoimmune Syndrome, Type I Polyendocrinopathy Candidiasis Ectodermal Dystrophy, Autoimmune Autoimmune Polyglandular Syndrome, Type 3 Deficiency, AIRE Syndrome, Schmidt's Autoimmune Polyglandular Syndrome, Type 1 Polyglandular Type II Autoimmune Syndrome Autoimmune Syndrome Type II, Polyglandular Diabetes Mellitus, Addison Disease, Myxedema Syndrome, Schmidt Schmidt's Syndrome
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| AN |
do not coordinate with specific endocrine disease term or CANDIDIASIS unless particularly discussed
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|
| AQL |
BL CF CI CL CN CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI
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|
| cui |
C0085859 C1535942 C0085409 C0085860
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|
| DC |
1
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|
| definition |
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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| DX |
19920101
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|
| HN |
1992
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| Inverse of AQ |
http://purl.bioontology.org/ontology/MESH/Q000097 http://purl.bioontology.org/ontology/MESH/Q000178 http://purl.bioontology.org/ontology/MESH/Q000175 http://purl.bioontology.org/ontology/MESH/Q000628 http://purl.bioontology.org/ontology/MESH/Q000276 http://purl.bioontology.org/ontology/MESH/Q000134 http://purl.bioontology.org/ontology/MESH/Q000139 http://purl.bioontology.org/ontology/MESH/Q000266 http://purl.bioontology.org/ontology/MESH/Q000378 http://purl.bioontology.org/ontology/MESH/Q000517 http://purl.bioontology.org/ontology/MESH/Q000662 http://purl.bioontology.org/ontology/MESH/Q000469 http://purl.bioontology.org/ontology/MESH/Q000151 http://purl.bioontology.org/ontology/MESH/Q000150 http://purl.bioontology.org/ontology/MESH/Q000821 http://purl.bioontology.org/ontology/MESH/Q000191 http://purl.bioontology.org/ontology/MESH/Q000196 http://purl.bioontology.org/ontology/MESH/Q000473 http://purl.bioontology.org/ontology/MESH/Q000145 http://purl.bioontology.org/ontology/MESH/Q000382 http://purl.bioontology.org/ontology/MESH/Q000451 http://purl.bioontology.org/ontology/MESH/Q000453 http://purl.bioontology.org/ontology/MESH/Q000534 http://purl.bioontology.org/ontology/MESH/Q000532 http://purl.bioontology.org/ontology/MESH/Q000503 http://purl.bioontology.org/ontology/MESH/Q000188 http://purl.bioontology.org/ontology/MESH/Q000235 http://purl.bioontology.org/ontology/MESH/Q000201 http://purl.bioontology.org/ontology/MESH/Q000209 http://purl.bioontology.org/ontology/MESH/Q000208 http://purl.bioontology.org/ontology/MESH/Q000601 http://purl.bioontology.org/ontology/MESH/Q000000981 http://purl.bioontology.org/ontology/MESH/Q000652 |
|
| Machine permutation |
1992
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| Mapped from |
http://purl.bioontology.org/ontology/MESH/C538273 |
|
| MDA |
19910502
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|
| MMR |
20130708
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|
| MN |
C20.111.750 C19.787
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| notation |
D016884
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| prefLabel |
Polyendocrinopathies, Autoimmune
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| TERMUI |
T812003 T781369 T781368 T811993 T840969 T050549 T781328 T781327 T781323 T840967 T781370 T050550 T844116 T781325 T811989 T781367 T817906 T781371 T637908 T050545 T840966 T812005 T050544 T637907 T844117 T781326 T050547 T050548 T840962 T811992 T750782 T050546 T817905 T817904
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| TH |
OMIM (2013) NLM (2012) NLM (1992) NLM (2010) GHR (2014) NLM (2006) ORD (2010)
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| tui |
T047
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| subClassOf |
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