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GTR Home > Conditions/Phenotypes > Vesicoureteral reflux 8

Vesicoureteral reflux 8

Summary

Any vesicoureteral reflux in which the cause of the disease is a mutation in the TNXB gene. [from MONDO]

Available tests

15 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (15 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

Associated genes Help
Genes reported to contribute to the condition.

TNXB
75 tests
Also known as: EDS3, EDSCLL, EDSCLL1, HXBL, TENX, TN-X, TNX, TNXB1, TNXB2, TNXBS, VUR8, XB, XBS, TNXB
Summary: tenascin XB

Imported from Human Phenotype Ontology (HPO)

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Abnormality of the genitourinary system
- Duplicated collecting system
  Duplicated collecting system
  - MedGen UID: 346936
  - Concept ID: C1858565
  - Finding: Anatomical Abnormality
  Abnormality of the genitourinary system
  See: Feature record | Search on this feature
- Recurrent urinary tract infections
  Recurrent urinary tract infections
  - MedGen UID: 120466
  - Concept ID: C0262655
  - Finding: Disease or Syndrome
  Abnormality of the genitourinary system
  See: Feature record | Search on this feature
- Vesicoureteral reflux
  Vesicoureteral reflux
  - MedGen UID: 21852
  - Concept ID: C0042580
  - Finding: Disease or Syndrome
  Abnormality of the genitourinary system
  See: Feature record | Search on this feature
Abnormality of the musculoskeletal system
- Joint hypermobility
  Joint hypermobility
  - MedGen UID: 336793
  - Concept ID: C1844820
  - Finding: Finding
  Abnormality of the musculoskeletal system
  See: Feature record | Search on this feature

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Clinical resources

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