Vesicoureteral reflux 2

Preferred Label : Vesicoureteral reflux 2;

Symbol : VUR2;

CISMeF acronym : VUR2;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutation in the roundabout guidance receptor 2 gene (ROBO2, 602431.0001);

Prefixed ID : #610878;

Details

Origin ID

610878;

UMLS CUI

C1970483;

Automatic exact mappings (from CISMeF team)
- Familial vesicoureteral reflux [ORDO Disease]
Currated CISMeF NLP mapping
- vesicoureteral reflux 2 [MeSH concept]
- vesicoureteral reflux 2 [MeSH Supplementary Concept]
DO Cross reference
- vesicoureteral reflux [DO Concept]
Genes related to phenotype
- Roundabout guidance receptor 2 [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Renal hypoplasia [HPO term]
- Vesicoureteral reflux [HPO term]
ORDO concept(s)
- Familial vesicoureteral reflux [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- vesicoureteral reflux 2 [MeSH Supplementary Concept]
- vesicoureteral reflux 2 [MeSH concept]

Keyword's position in hierarchy(ies) :

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