Vesicoureteral reflux 3

Preferred Label : Vesicoureteral reflux 3;

Symbol : VUR3;

CISMeF acronym : VUR3;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutation in the SRY-box 17 gene (SOX17, 610928.0001);

Prefixed ID : #613674;

Details

Origin ID

613674;

UMLS CUI

C3150927;

Automatic exact mappings (from CISMeF team)
- Familial vesicoureteral reflux [ORDO Disease]
- SOX17 wt Allele [NCIt concept]
DO Cross reference
- vesicoureteral reflux [DO Concept]
Genes related to phenotype
- Sry-box 17 [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Hydronephrosis [HPO term]
- Hydroureter [HPO term]
- Polyhydramnios [HPO term]
- Vesicoureteral reflux [HPO term]
ORDO concept(s)
- Familial vesicoureteral reflux [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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