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Familial vesicoureteral reflux
7 OMIM references -
2 associated genes
9 connected diseases
No signs/symptoms info
Disease Type of connection
Burkitt lymphoma
Precursor T-cell acute lymphoblastic leukemia
Autosomal dominant nonsyndromic intellectual deficit
Craniopharyngioma
Desmoid tumor
Hepatocellular carcinoma, childhood-onset
Pilomatrixoma
Chronic berylliosis
Granulomatosis with polyangiitis
Synonym(s):
- Familial VUR
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare urogenital disease
Classification (ICD10):
- Diseases of the genitourinary system -
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
External references:
7 OMIM references -
No MeSH references
Gene symbol UniProt reference OMIM reference
ROBO2 Q9HCK4602431
SOX17 Q9H6I2610928
No signs/symptoms info available.