Idiopathic Retroperitoneal Fibrosis

Preferred Label : Idiopathic Retroperitoneal Fibrosis;

NCIt related terms : Ormond's Disease;

Alternative definition : NICHD: A condition characterized by abnormal proliferation of fibrous tissue in the compartment posterior to the peritoneum, for which no underlying cause has been identified.;

Details

Origin ID

C123249;

UMLS CUI

C4048297;

Automatic exact mappings (from CISMeF team)
- Idiopathic retroperitoneal fibrosis [MedDRA LLT]
- Idiopathic retroperitoneal fibrosis (disorder) [SNOMED CT concept]
- IgG4-related retroperitoneal fibrosis [ORDO Disease]
- Primary retroperitoneal fibrosis [ICD-11 Sub-sub category]
- Retroperitoneal fibrosis [MedDRA Preferred Term]
- Retroperitoneal fibrosis [ICD-11 Subcategory]
- Retroperitoneal fibrosis (disorder) [SNOMED CT concept]
- retroperitoneal fibrosis [MeSH Descriptor]
Has associated anatomic sites
- Peritoneum and Retroperitoneum [NCIt concept]
- Retroperitoneum [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Idiopathic retroperitoneal fibrosis [MedDRA LLT]
- Idiopathic retroperitoneal fibrosis (disorder) [SNOMED CT concept]
- Ormond's disease [MedDRA LLT]
concept_is_in_subset
- NICHD Terminology [NCIt concept]
- Pediatric Nephrology Terminology [NCIt concept]
disease_has_primary_anatomic_site
- Peritoneum and Retroperitoneum [NCIt concept]
- Retroperitoneum [NCIt concept]

Keyword's position in hierarchy(ies) :

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