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National Drug File - Reference Terminology
Last uploaded:
July 6, 2018
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| Preferred Name | Polyendocrinopathies, Autoimmune [Disease/Finding] | |
| Synonyms |
Polyendocrinopathies, Autoimmune |
|
| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000003500 |
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| altLabel |
Polyendocrinopathies, Autoimmune
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|
| cui |
C0085409
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| MESH 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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| MESH DUI |
D016884
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|
| MeSH name |
Polyendocrinopathies, Autoimmune
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|
| MESH UI |
M0025689
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|
| NDFRT kind |
DISEASE_KIND
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|
| notation |
N0000003500
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|
| NUI |
N0000003500
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|
| prefLabel |
Polyendocrinopathies, Autoimmune [Disease/Finding]
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|
| SNOMED CID |
41864002
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|
| tui |
T047
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| subClassOf |
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