Hydroureter
Symptom Information:
Symptom ID: | HPO:0000072 | |||||||||||||||||||||||||
Synonyms: |
|
|||||||||||||||||||||||||
Quality: | ||||||||||||||||||||||||||
Cross references: |
|
|||||||||||||||||||||||||
Is a (Direct Parents): |
|
|||||||||||||||||||||||||
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) |