Vesicoureteral reflux 8

Preferred Label : Vesicoureteral reflux 8;

Symbol : VUR8;

CISMeF acronym : VUR8;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutation in the tenascin XB gene (TNXB, 600985.0006);

Prefixed ID : #615963;

Details

Origin ID

615963;

UMLS CUI

C4014831;

DO Cross reference
- vesicoureteral reflux [DO Concept]
Genes related to phenotype
- Tenascin xb [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Duplicated collecting system [HPO term]
- Joint hypermobility [HPO term]
- Recurrent urinary tract infections [HPO term]
- Vesicoureteral reflux [HPO term]
ORDO concept(s)
- Familial vesicoureteral reflux [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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