Autoimmune Hypophysitis

Preferred Label : Autoimmune Hypophysitis;

NCIt related terms : Lymphocytic Hypophysitis;

Alternative definition : NICHD: An autoimmune condition affecting the pituitary gland, characterized by lymphocytic infiltration, commonly presenting with pituitary hormone deficiencies.;

Details

Origin ID

C132055;

UMLS CUI

C0342410;

Automatic exact mappings (from CISMeF team)
- Autoimmune Hypophysitis [MeSH Descriptor]
- Autoimmune Hypophysitis [MeSH concept]
- Autoimmune hypophysitis [MedDRA LLT]
- Autoimmune hypophysitis (disorder) [SNOMED CT concept]
- Lymphocytic hypophysitis [MedDRA Preferred Term]
- Lymphocytic hypophysitis [ICD-11 More detail]
- Lymphocytic hypopituitarism (disorder) [SNOMED CT concept]
- Primary hypophysitis [ORDO Disease]
- lymphocytic hypophysitis [Radlex concept]
Has associated anatomic sites
- Head and Neck [NCIt concept]
- Pituitary Gland [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autoimmune Hypophysitis [MeSH Descriptor]
- Autoimmune hypophysitis [MedDRA LLT]
- Autoimmune hypophysitis (disorder) [SNOMED CT concept]
- Primary hypophysitis [ORDO Disease]
concept_is_in_subset
- NICHD Terminology [NCIt concept]
- Pediatric Endocrinology Terminology [NCIt concept]
disease_has_primary_anatomic_site
- Pituitary Gland [NCIt concept]

Keyword's position in hierarchy(ies) :

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