Autoimmune Polyendocrinopathy Syndrome

Preferred Label : Autoimmune Polyendocrinopathy Syndrome;

NCIt synonyms : Autoimmune Polyendocrinopathy;

NCIt definition : A rare genetic syndrome characterized by autoantibodies production against more than one endocrine organ. The range of endocrinopathies includes hypoparathyroidism, adrenal insufficiency, hypogonadism, type 1 diabetes mellitus and hypothyroidism.;

Détails

Origin ID

C84576;

UMLS CUI

C0085409;

Currated CISMeF NLP mapping
- Autoimmune polyendocrinopathy [ICD-11 Category]
- Autoimmune polyendocrinopathy [ORDO Disease]
- 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]
DO Cross reference
- autoimmune polyendocrine syndrome [DO Concept]
Has associated anatomic sites
- Endocrine Gland [NCIt concept]
- Endocrine System [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autoimmune polyendocrinopathy [ORDO Disease]
- Autoimmune polyendocrinopathy [ICD-11 Category]
- Autoimmune polyendocrinopathy (disorder) [SNOMED CT concept]
- Autoimmune polyglandular failure [ICD-10 Sub-category]
- autoimmune polyendocrine syndrome [DO Concept]
- autoimmune polyendocrinopathy [Disease (Nov.)]
- autoimmune polyendocrinopathy, nos [SNOMED Notion]
- lloyd's syndrome [SNOMED Notion]
- polyendocrinopathies, autoimmune [MeSH Descriptor]
- polyendocrinopathies, autoimmune [MeSH concept]
disease_has_finding
- Rare Lesion [NCIt concept]
disease_has_primary_anatomic_site
- Endocrine System [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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