Autoimmune Polyglandular Syndrome

Preferred Label : Autoimmune Polyglandular Syndrome;

NCIt related terms : Polyglandular Autoimmune Syndrome; Autoimmune Polyendocrine Syndrome; Autoimmune Polyglandular Syndrome(s);

Alternative definition : NICHD: A group of diverse conditions that are characterized by spontaneous, multi-organ autoimmunity, which target both endocrine (adrenal, gonad, pancreatic islet cells, parathyroid, pituitary, thyroid) and non-endocrine (gastrointestinal, integumentary, lymphatic) tissues.;

NCI Metathesaurus CUI : CL513017;

Details

Origin ID

C129726;

UMLS CUI

C4316913;

Currated CISMeF NLP mapping
- Autoimmune polyendocrinopathy [ORDO Disease]
- Autoimmune polyendocrinopathy [ICD-11 Category]
- Autoimmune polyendocrinopathy (disorder) [SNOMED CT concept]
- autoimmune polyendocrine syndrome [DO Concept]
- autoimmune polyendocrinopathy [Disease (Nov.)]
- autoimmune polyendocrinopathy, nos [SNOMED Notion]
- polyendocrinopathies, autoimmune [MeSH Descriptor]
- polyendocrinopathies, autoimmune [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
concept_is_in_subset
- CTRP Disease Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
- NICHD Terminology [NCIt concept]
- Pediatric Endocrinology Terminology [NCIt concept]

Keyword's position in hierarchy(ies) :

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