Vesicoureteral reflux
Symptom Information:
Symptom ID: | HPO:0000076 | ||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |