Renal Agenesis

Preferred Label : Renal Agenesis;

NCIt definition : A congenital abnormality characterized by the absence of one or both kidneys.;

Details

Origin ID

C99041;

UMLS CUI

C0542519;

Automatic exact mappings (from CISMeF team)
- renal agenesis [DO Concept]
Currated CISMeF NLP mapping
- Kidney agenesis [PASCAL descriptor]
- Oligohydramnios sequence (disorder) [SNOMED CT concept]
- RENAL AGENESIS [WHO-ART Preferred Term]
- Renal agenesis [HPO term]
- Renal agenesis [MedDRA LLT]
- Renal agenesis [ORDO Disease]
- Renal agenesis [ICD-11 Sub-sub category]
- Renal agenesis (disorder) [SNOMED CT concept]
- Renal agenesis, unspecified [ICD-10 Sub-category (who)]
- Renal agenesis, unspecified [ICD-10 Sub-category]
- Renal aplasia [MedDRA Preferred Term]
- Renal dysplasia/aplasia [HPO term]
- Renal hypodysplasia/aplasia 1 [OMIM Phenotype]
- hereditary renal agenesis [MeSH Supplementary Concept]
- renal adysplasia [MeSH Supplementary Concept]
- renal adysplasia [MeSH concept]
- renal agenesis [Radlex concept]
Has associated anatomic sites
- Genitourinary System [NCIt concept]
- Urinary System [NCIt concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Kidney agenesis [PASCAL descriptor]
- RENAL AGENESIS [WHO-ART Preferred Term]
- Renal agenesis [MedDRA LLT]
- Renal agenesis [HPO term]
- Renal agenesis (disorder) [SNOMED CT concept]
- Renal agenesis congenital [MedDRA LLT]
- Renal agenesis, unspecified [ICD-10 Sub-category]
- renal agenesis [Radlex concept]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
- NICHD Terminology [NCIt concept]
- Neonatal Research Network Terminology [NCIt concept]
disease_has_primary_anatomic_site
- Genitourinary System [NCIt concept]
- Urinary System [NCIt concept]

Keyword's position in hierarchy(ies) :

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