Hydroureter

Symptom Information:

Symptom ID: HPO:0000072
Synonyms:
Megaureter [HPO:0000072]
Ureteral dilatation [HPO:0000072]
Uroureter [HPO:0000072]
Megaureter [Orphanet:37720]
Hydroureter (disorder) [Orphanet:37720]
Megaloureter - congenital [Orphanet:37720]
Congenital dilatation of ureter [Orphanet:37720]
Dilatation of ureter [Orphanet:37720]
Hydroureter [OMIM:Hydroureter]
Megaureter [OMIM:Megaureter]
Ureteral dilatation [OMIM:Ureteral dilatation]
Megaureter/hydronephrosis/pyeloureteral junction syndrome [Orphanet:37720]
Ureteric dilatation [Orphanet:37720]
Hydroureter [Orphanet:37720]
Congenital megaureter [Orphanet:37720]
Ureteric dilatation [MedDRA:10046399]
Dilatation ureteral [MedDRA:10046399]
Distended ureter [MedDRA:10046399]
Hydroureter [MedDRA:10020533]
Congenital megaureter [MedDRA:10010540]
Congenital hydroureter [MedDRA:10010540]
Ureterovesical junction obstruction [MedDRA:10010540]
Congenital megaloureters [OMIM:Congenital megaloureters]
Hydroureters [OMIM:Hydroureters]
Ureteric dilatation (in 1 of 6 patients) [OMIM:Ureteric dilatation (in 1 of 6 patients)]
Quality:
Cross references:
Orphanet:37720 "Megaureter/hydronephrosis/pyeloureteral junction syndrome" [Orphanet:37720]
OMIM: "Hydroureter" [OMIM:Hydroureter]
OMIM: "Megaureter" [OMIM:Megaureter]
OMIM: "Ureteral dilatation" [OMIM:Ureteral dilatation]
OMIM: "Congenital megaloureters" [OMIM:Congenital megaloureters]
OMIM: "Hydroureters" [OMIM:Hydroureters]
OMIM: "Ureteric dilatation (in 1 of 6 patients)" [OMIM:Ureteric dilatation (in 1 of 6 patients)]
UMLS:C0266324 "Congenital dilatation of ureter" [Orphanet:37720]
UMLS:C0521620 "Dilatation of ureter" [Orphanet:37720]
Is a (Direct Parents):
MedDRA Ureteric disorders congenital
HPO         Abnormality of the ureter
Orphanet Bladder and ureter anomalies
MedDRA Ureteric disorders NEC
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 upper urinary tract(HPO:0010935)
                Abnormality of the ureter(HPO:0000069)
                   Hydroureter(HPO:0000072)
MedDRA:
Renal and urinary disorders(MedDRA:10038359)
    Ureteric disorders(MedDRA:10046400)
       Ureteric disorders congenital(MedDRA:10046401)
          Hydroureter(HPO:0000072)
       Ureteric disorders NEC(MedDRA:10046402)
          Hydroureter(HPO:0000072)
Database Frequency: 146 / 7739
Resource:

All diseases associated with this symptom:

1p36 deletion syndrome (Orphanet:1606)
1q21.1 microdeletion syndrome (Orphanet:250989)
22q11.2 microduplication syndrome (Orphanet:1727)
2p15p16.1 microdeletion syndrome (Orphanet:261349)
3C syndrome (Orphanet:7)
46,XX disorder of sex development - anorectal anomalies (Orphanet:2973)
6p22 microdeletion syndrome (Orphanet:251046)
8p23.1 microduplication syndrome (Orphanet:251076)
Alpha-thalassemia - X-linked intellectual deficit syndrome (Orphanet:847)
Alström syndrome (Orphanet:64)
Autosomal dominant Robinow syndrome (Orphanet:3107)
Autosomal recessive Robinow syndrome (Orphanet:1507)
Axial mesodermal dysplasia spectrum (Orphanet:1834)
BOR syndrome (Orphanet:107)
Baller-Gerold syndrome (Orphanet:1225)
Baraitser-Winter syndrome (Orphanet:2995)
Beta-ureidopropionase deficiency (Orphanet:65287)
Bilateral multicystic renal dysplasia (Orphanet:97364)
Bladder exstrophy (Orphanet:93930)
Branchio-oculo-facial syndrome (Orphanet:1297)
CARDIAC VALVULAR DEFECT, DEVELOPMENTAL (OMIM:212093)
CARPENTER SYNDROME 1 (OMIM:201000)
CHARGE syndrome (Orphanet:138)
CHILD syndrome (Orphanet:139)
CODAS syndrome (Orphanet:1458)
Campomelic dysplasia (Orphanet:140)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Carey-Fineman-Ziter syndrome (Orphanet:1358)
Carpenter syndrome (Orphanet:65759)
Cat-eye syndrome (Orphanet:195)
Caudal regression sequence (Orphanet:3027)
Cholestasis - pigmentary retinopathy - cleft palate (Orphanet:1415)
Cloacal exstrophy (Orphanet:93929)
Coffin-Siris syndrome (Orphanet:1465)
Congenital alveolar capillary dysplasia (Orphanet:210122)
Congenital hydronephrosis (Orphanet:2190)
Congenital primary megaureter (Orphanet:617)
Congenital unilateral hypoplasia of depressor anguli oris (Orphanet:1166)
Corneal anesthesia - deafness - intellectual deficit (Orphanet:1051)
Craniomicromelic syndrome (Orphanet:1524)
Craniosynostosis, Herrmann-Opitz type (Orphanet:2145)
Currarino triad (Orphanet:1552)
DYSMYELINATION WITH JAUNDICE (OMIM:224250)
Deafness - onychodystrophy (Orphanet:3231)
Desmoid tumor (Orphanet:873)
Diabetic embryopathy (Orphanet:1926)
Distal trisomy 14q (Orphanet:1705)
Dubowitz syndrome (Orphanet:235)
Dysmorphism - multiple structural anomalies (Orphanet:1780)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1 (OMIM:129900)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 (OMIM:604292)
EEC syndrome (Orphanet:1896)
Ellis Van Creveld syndrome (Orphanet:289)
Erdheim-Chester disease (Orphanet:35687)
Exstrophy-epispadias complex (Orphanet:322)
Facial ectodermal dysplasia (Orphanet:1807)
Faciocardiorenal syndrome (Orphanet:1973)
Familial caudal dysgenesis (Orphanet:1768)
Familial visceral myopathy (Orphanet:2604)
Focal dermal hypoplasia (Orphanet:2092)
Frontometaphyseal dysplasia (Orphanet:1826)
Fryns syndrome (Orphanet:2059)
Genitopatellar syndrome (Orphanet:85201)
Granulomatosis with polyangiitis (Orphanet:900)
Hereditary orotic aciduria (Orphanet:30)
Hermansky-Pudlak syndrome (Orphanet:79430)
Hinman syndrome (Orphanet:84085)
Hirschsprung disease - nail hypoplasia - dysmorphism (Orphanet:2153)
Humero-radio-ulnar synostosis (Orphanet:3266)
IMAGe syndrome (Orphanet:85173)
Ichthyosis follicularis - alopecia - photophobia (Orphanet:2273)
Intellectual deficit, Buenos-Aires type (Orphanet:3079)
Intellectual deficit, X-linked, Wittwer type (Orphanet:85291)
Jacobsen syndrome (Orphanet:2308)
Johanson-Blizzard syndrome (Orphanet:2315)
Junctional epidermolysis bullosa, non-Herlitz type (Orphanet:89840)
Kabuki syndrome (Orphanet:2322)
Kleefstra syndrome (Orphanet:261494)
Koolen-De Vries syndrome (Orphanet:96169)
Lethal chondrodysplasia, Moerman type (Orphanet:1420)
Lethal multiple pterygium syndrome (Orphanet:33108)
MICROPHTHALMIA, SYNDROMIC 1 (OMIM:309800)
Marden-Walker syndrome (Orphanet:2461)
McKusick-Kaufman syndrome (Orphanet:2473)
Meckel syndrome (Orphanet:564)
Megacystis-microcolon-intestinal hypoperistalsis syndrome (Orphanet:2241)
Mesomelia-synostoses syndrome (Orphanet:2496)
Micrencephaly - corpus callosum agenesis - abnormal genitalia (Orphanet:2508)
Micro syndrome (Orphanet:2510)
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 (Orphanet:2636)
Microlissencephaly - micromelia (Orphanet:50810)
Microphthalmia - microtia - fetal akinesia (Orphanet:2547)
Microphthalmia, Lenz type (Orphanet:568)
Monosomy 9p (Orphanet:261112)
Mosaic trisomy 8 (Orphanet:96061)
Mosaic trisomy 9 (Orphanet:99776)
Mowat-Wilson syndrome (Orphanet:2152)
Mullerian derivatives - lymphangiectasia - polydactyly (Orphanet:1655)
Multicystic renal dysplasia (Orphanet:1851)
Multiple non-ossifying fibromatosis (Orphanet:2029)
Nephrosis - deafness - urinary tract - digital malformations (Orphanet:2669)
Netherton syndrome (Orphanet:634)
Nijmegen breakage syndrome (Orphanet:647)
Non-rhizomelic chondrodysplasia punctata (Orphanet:176)
Ochoa syndrome (Orphanet:2704)
Oculoauriculovertebral spectrum with radial defects (Orphanet:2549)
Oculocerebral hypopigmentation syndrome, Cross type (Orphanet:2719)
Okamoto syndrome (Orphanet:2729)
Orofaciodigital syndrome type 1 (Orphanet:2750)
Osteodysplasty, Melnick-Needles type (Orphanet:2484)
Otopalatodigital syndrome type 2 (Orphanet:90652)
PRUNE BELLY SYNDROME WITH PULMONIC STENOSIS, MENTAL RETARDATION, ANDDEAFNESS (OMIM:264140)
Peters-plus syndrome (Orphanet:709)
Pfeiffer syndrome type 3 (Orphanet:93260)
Postaxial polydactyly - dental and vertebral anomalies (Orphanet:2916)
Prominent glabella - microcephaly - hypogenitalism (Orphanet:2083)
Prune belly syndrome (Orphanet:2970)
Rabson-Mendenhall syndrome (Orphanet:769)
Renal caliceal diverticuli - deafness (Orphanet:2838)
Renal dysplasia - megalocystis - sirenomelia (Orphanet:1850)
Ring chromosome 8 (Orphanet:1450)
Schinzel-Giedion syndrome (Orphanet:798)
Schwartz-Jampel syndrome (Orphanet:800)
Short rib-polydactyly syndrome, Verma-Naumoff type (Orphanet:93271)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Split hand - urinary anomalies - spina bifida (Orphanet:2437)
Spondylocostal dysostosis - anal and genitourinary malformations (Orphanet:94095)
Steinert myotonic dystrophy (Orphanet:273)
Syndactyly - telecanthus - anogenital and renal malformations (Orphanet:140952)
Tetraploidy (Orphanet:3305)
Toluene embryopathy (Orphanet:1920)
Trisomy 13 (Orphanet:3378)
Trisomy 17p (Orphanet:261290)
Trisomy 18 (Orphanet:3380)
Trisomy 1q (Orphanet:261344)
Trisomy 20p (Orphanet:261318)
UROFACIAL SYNDROME 1 (OMIM:236730)
VACTERL/VATER association (Orphanet:887)
VESICOURETERAL REFLUX 3 (OMIM:613674)
Van Regemorter-Pierquin-Vamos syndrome (Orphanet:3419)
Walker-Warburg syndrome (Orphanet:899)
Wolfram syndrome 1 (OMIM:222300)
Wolfram syndrome, mitochondrial form (OMIM:598500)
Zellweger syndrome (Orphanet:912)
Zunich-Kaye syndrome (Orphanet:3474)