Vesicoureteral reflux

Symptom Information:

Symptom ID: HPO:0000076
Synonyms:
Ureteral reflux [HPO:0000076]
Ureteric reflux [HPO:0000076]
Vesicoureteric reflux [HPO:0000076]
Vesicoureteric reflux (disorder) [Orphanet:37800]
Vesico-Ureteral Reflux [Orphanet:37800]
Ureteral reflux [OMIM:Ureteral reflux]
Ureteric reflux [OMIM:Ureteric reflux]
Vesicoureteral reflux [OMIM:Vesicoureteral reflux]
Vesicoureteric reflux [OMIM:Vesicoureteric reflux]
Vesicorenal/vesicoureteral reflux [Orphanet:37800]
Vesicoureteric reflux [Orphanet:37800]
Vesicoureteric reflux [MedDRA:10047370]
Ureteric reflux [MedDRA:10047370]
Vesicoureteral reflux [MedDRA:10047370]
Vesicouretral reflux unspecified or without reflux nephropathy [MedDRA:10047370]
Vesicoureteral reflux (1 patient) [OMIM:Vesicoureteral reflux (1 patient)]
Vesicoureteral reflux (in 1 patient) [OMIM:Vesicoureteral reflux (in 1 patient)]
Vesicoureteral reflux (less common) [OMIM:Vesicoureteral reflux (less common)]
Vesicoureteral reflux (rare) [OMIM:Vesicoureteral reflux (rare)]
Vesicoureteral reflux (seen in patients with contiguous gene defect) [OMIM:Vesicoureteral reflux (seen in patients with contiguous gene defect)]
Vesicoureteral reflux (variable) [OMIM:Vesicoureteral reflux (variable)]
Vesicoureteric reflux (less common) [OMIM:Vesicoureteric reflux (less common)]
Quality:
Cross references:
Orphanet:37800 "Vesicorenal/vesicoureteral reflux" [Orphanet:37800]
OMIM: "Ureteral reflux" [OMIM:Ureteral reflux]
OMIM: "Ureteric reflux" [OMIM:Ureteric reflux]
OMIM: "Vesicoureteral reflux" [OMIM:Vesicoureteral reflux]
OMIM: "Vesicoureteric reflux" [OMIM:Vesicoureteric reflux]
OMIM: "Vesicoureteral reflux (1 patient)" [OMIM:Vesicoureteral reflux (1 patient)]
OMIM: "Vesicoureteral reflux (in 1 patient)" [OMIM:Vesicoureteral reflux (in 1 patient)]
OMIM: "Vesicoureteral reflux (less common)" [OMIM:Vesicoureteral reflux (less common)]
OMIM: "Vesicoureteral reflux (rare)" [OMIM:Vesicoureteral reflux (rare)]
OMIM: "Vesicoureteral reflux (seen in patients with contiguous gene defect)" [OMIM:Vesicoureteral reflux (seen in patients with contiguous gene defect)]
OMIM: "Vesicoureteral reflux (variable)" [OMIM:Vesicoureteral reflux (variable)]
OMIM: "Vesicoureteric reflux (less common)" [OMIM:Vesicoureteric reflux (less common)]
UMLS:C0042580 "Vesico-Ureteral Reflux" [Orphanet:37800]
Is a (Direct Parents):
HPO         Abnormality of the ureter
MedDRA Bladder reflux conditions
HPO         Functional abnormality of the bladder
Orphanet Bladder and ureter anomalies
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the genitourinary system(HPO:0000119)
          Abnormality of the urinary system(HPO:0000079)
             Abnormality of the lower urinary tract(HPO:0010936)
                Abnormality of the bladder(HPO:0000014)
                   Functional abnormality of the bladder(HPO:0000009)
                      Vesicoureteral reflux(HPO:0000076)
             Abnormality of the upper urinary tract(HPO:0010935)
                Abnormality of the ureter(HPO:0000069)
                   Vesicoureteral reflux(HPO:0000076)
MedDRA:
Renal and urinary disorders(MedDRA:10038359)
    Bladder and bladder neck disorders (excl calculi)(MedDRA:10004994)
       Bladder reflux conditions(MedDRA:10005069)
          Vesicoureteral reflux(HPO:0000076)
Database Frequency: 94 / 7739
Resource:

All diseases associated with this symptom:

1q21.1 microdeletion syndrome (Orphanet:250989)
22q11.2 deletion syndrome (Orphanet:567)
8q12 microduplication syndrome (Orphanet:228399)
Acro-pectoro-renal dysplasia (Orphanet:956)
Acro-renal-ocular syndrome (Orphanet:959)
Alagille syndrome due to 20p12 microdeletion (Orphanet:261600)
Alagille syndrome due to a JAG1 point mutation (Orphanet:261619)
Alström syndrome (Orphanet:64)
Atrioventricular defect - blepharophimosis -radial defects (Orphanet:1352)
Autosomal recessive cutis laxa type 1 (Orphanet:90349)
BOR syndrome (Orphanet:107)
BRANCHIOOTORENAL SYNDROME 1 (OMIM:113650)
BRESEK syndrome (Orphanet:85284)
Baller-Gerold syndrome (Orphanet:1225)
Beckwith-Wiedemann syndrome due to NSD1 mutation (Orphanet:238613)
Bladder exstrophy (Orphanet:93930)
Bohring-Opitz syndrome (Orphanet:97297)
CHARGE syndrome (Orphanet:138)
CHROMOSOME 1p32-p31 DELETION SYNDROME (OMIM:613735)
CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT, SUSCEPTIBILITY TO (OMIM:610805)
CORNELIA DE LANGE SYNDROME 1 (OMIM:122470)
CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG (OMIM:218649)
Cardiocranial syndrome, Pfeiffer type (Orphanet:2872)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Carpenter-Waziri syndrome (Orphanet:93973)
Caudal regression sequence (Orphanet:3027)
Cholestasis - pigmentary retinopathy - cleft palate (Orphanet:1415)
Chudley-Lowry-Hoar syndrome (Orphanet:93971)
Cloacal exstrophy (Orphanet:93929)
Congenital primary megaureter (Orphanet:617)
Cornelia de Lange syndrome (Orphanet:199)
Currarino triad (Orphanet:1552)
Cutis laxa (Orphanet:209)
DIAMOND-BLACKFAN ANEMIA 7 (OMIM:612562)
DUAL SERINE/THREONINE AND TYROSINE PROTEIN KINASE (OMIM:612666)
Dislocation of the hip - dysmorphism (Orphanet:2412)
Distal monosomy 10q (Orphanet:96148)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1 (OMIM:129900)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 (OMIM:604292)
EEC syndrome (Orphanet:1896)
Ehlers-Danlos syndrome due to tenascin-X deficiency (Orphanet:230839)
Epispadias (Orphanet:93928)
Familial vesicoureteral reflux (Orphanet:289365)
Familial visceral myopathy (Orphanet:2604)
Fryns syndrome (Orphanet:2059)
Goldenhar syndrome (Orphanet:374)
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2 (OMIM:614749)
Hand-foot-genital syndrome (Orphanet:2438)
Hennekam syndrome (Orphanet:2136)
Hinman syndrome (Orphanet:84085)
Holmes-Gang syndrome (Orphanet:93970)
Hypoparathyroidism - deafness - renal disease (Orphanet:2237)
Juberg-Marsidi syndrome (Orphanet:93972)
KERATOCONUS POSTICUS CIRCUMSCRIPTUS (OMIM:244600)
Kleefstra syndrome (Orphanet:261494)
Kleefstra syndrome due to 9q34 microdeletion (Orphanet:96147)
Knobloch syndrome (Orphanet:1571)
Koolen-De Vries syndrome (Orphanet:96169)
Langer-Giedion syndrome (Orphanet:502)
MUNGAN SYNDROME (OMIM:611376)
MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,AND PSYCHOMOTOR DELAY (OMIM:601347)
Matthew-Wood syndrome (Orphanet:2470)
Microcephaly-capillary malformation syndrome (Orphanet:294016)
Monosomy 22q13 (Orphanet:48652)
Mosaic trisomy 8 (Orphanet:96061)
Mowat-Wilson syndrome (Orphanet:2152)
Mulibrey nanism (Orphanet:2576)
Multiple congenital anomalies - hypotonia - seizures syndrome (Orphanet:280633)
Multiple congenital anomalies-hypotonia-seizures syndrome type 2 (Orphanet:300496)
Nephronophthisis 12 (OMIM:613820)
Ochoa syndrome (Orphanet:2704)
Okihiro syndrome (Orphanet:93293)
Osteodysplasty, Melnick-Needles type (Orphanet:2484)
PELVIS syndrome (Orphanet:83628)
Pfeiffer syndrome type 3 (Orphanet:93260)
Prune belly syndrome (Orphanet:2970)
RENAL DYSPLASIA, CYSTIC, SUSCEPTIBILITY TO (OMIM:601331)
Renal coloboma syndrome (Orphanet:1475)
Renier-Gabreels-Jasper syndrome (Orphanet:93975)
Schinzel-Giedion syndrome (Orphanet:798)
Smith-Fineman-Myers syndrome (Orphanet:93974)
Syndactyly - telecanthus - anogenital and renal malformations (Orphanet:140952)
Townes-Brocks syndrome (Orphanet:857)
UROFACIAL SYNDROME 2 (OMIM:615112)
VACTERL/VATER association (Orphanet:887)
VESICOURETERAL REFLUX 1 (OMIM:193000)
VESICOURETERAL REFLUX 2 (OMIM:610878)
VESICOURETERAL REFLUX 3 (OMIM:613674)
VESICOURETERAL REFLUX 8 (OMIM:615963)
VESICOURETERAL REFLUX, X-LINKED (OMIM:314550)
WEBB-DATTANI SYNDROME (OMIM:615926)
Williams syndrome (Orphanet:904)
Wolfram syndrome 1 (OMIM:222300)
X-linked intellectual deficit - hypotonic face (Orphanet:73220)