Hydronephrosis
Symptom Information:
Symptom ID: | HPO:0000126 | ||||||||||||||
Synonyms: |
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Quality: | |||||||||||||||
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 upper urinary tract(HPO:0010935) Abnormality of the kidney(HPO:0000077) Abnormal renal morphology(HPO:0012210) Abnormality of the renal pelvis(HPO:0010944) Dilatation of the renal pelvis(HPO:0010946) Hydronephrosis(HPO:0000126) MedDRA: Renal and urinary disorders(MedDRA:10038359) Nephropathy(HPO:0000112) Renal obstructive disorders(MedDRA:10038488) Hydronephrosis(HPO:0000126) |
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Database Frequency: | 119 / 7739 | ||||||||||||||
Resource: |
All diseases associated with this symptom:
17q12 microdeletion syndrome | (Orphanet:261265) |
22q11.2 deletion syndrome | (Orphanet:567) |
2p15p16.1 microdeletion syndrome | (Orphanet:261349) |
3C syndrome | (Orphanet:7) |
3MC SYNDROME 1 | (OMIM:257920) |
AMASTIA, BILATERAL, WITH URETERAL TRIPLICATION AND DYSMORPHISM | (OMIM:104350) |
Acro-renal-ocular syndrome | (Orphanet:959) |
Alpha-thalassemia - X-linked intellectual deficit syndrome | (Orphanet:847) |
Apert syndrome | (Orphanet:87) |
Autosomal dominant Robinow syndrome | (Orphanet:3107) |
Autosomal recessive Robinow syndrome | (Orphanet:1507) |
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency | (Orphanet:331176) |
Bardet-Biedl syndrome 1 | (OMIM:209900 ) |
Bardet-Biedl syndrome 10 | (OMIM:615987) |
Bardet-Biedl syndrome 12 | (OMIM:615989) |
Bardet-Biedl syndrome 6 | (OMIM:605231) |
Bardet-Biedl syndrome 7 | (OMIM:615984) |
Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11 | (Orphanet:96193) |
Bilateral multicystic renal dysplasia | (Orphanet:97364) |
CAMPOMELIC DYSPLASIA | (OMIM:114290) |
CARDIAC VALVULAR DEFECT, DEVELOPMENTAL | (OMIM:212093) |
CARDIOFACIOCUTANEOUS SYNDROME 1 | (OMIM:115150) |
CARPENTER SYNDROME 1 | (OMIM:201000) |
CHARGE syndrome | (Orphanet:138) |
CHILD syndrome | (Orphanet:139) |
CHROMOSOME 1p32-p31 DELETION SYNDROME | (OMIM:613735) |
COFFIN-SIRIS SYNDROME | (OMIM:135900) |
CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG | (OMIM:218649) |
Campomelic dysplasia | (Orphanet:140) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Carnitine palmitoyl transferase II deficiency, neonatal form | (Orphanet:228308) |
Carpenter syndrome | (Orphanet:65759) |
Cholestasis - pigmentary retinopathy - cleft palate | (Orphanet:1415) |
Cloacal exstrophy | (Orphanet:93929) |
Coffin-Siris syndrome | (Orphanet:1465) |
Congenital alveolar capillary dysplasia | (Orphanet:210122) |
Congenital short bowel syndrome | (Orphanet:2301) |
Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies | (Orphanet:221145) |
DIABETES INSIPIDUS, NEUROHYPOPHYSEAL TYPE | (OMIM:304900) |
DYSMYELINATION WITH JAUNDICE | (OMIM:224250) |
Diabetic embryopathy | (Orphanet:1926) |
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, MUSCULOCONTRACTURAL TYPE 1 | (OMIM:601776) |
Ehlers-Danlos syndrome, musculocontractural type | (Orphanet:2953) |
Encephalocraniocutaneous lipomatosis | (Orphanet:2396) |
Exstrophy-epispadias complex | (Orphanet:322) |
FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS | (OMIM:227255) |
FANCONI ANEMIA, COMPLEMENTATION GROUP O | (OMIM:613390) |
Familial visceral myopathy | (Orphanet:2604) |
Floating-Harbor syndrome | (Orphanet:2044) |
Focal dermal hypoplasia | (Orphanet:2092) |
Frontometaphyseal dysplasia | (Orphanet:1826) |
Fryns syndrome | (Orphanet:2059) |
Genitopatellar syndrome | (Orphanet:85201) |
HOLOPROSENCEPHALY 3 | (OMIM:142945) |
HYDROLETHALUS SYNDROME 1 | (OMIM:236680) |
Hennekam syndrome | (Orphanet:2136) |
Hereditary xanthinuria | (Orphanet:3467) |
Hirschsprung disease - nail hypoplasia - dysmorphism | (Orphanet:2153) |
Holoprosencephaly | (Orphanet:2162) |
Hydrolethalus | (Orphanet:2189) |
INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, X-LINKED | (OMIM:300048) |
Intellectual deficit, X-linked - craniofacioskeletal syndrome | (Orphanet:163979) |
Johanson-Blizzard syndrome | (Orphanet:2315) |
Koolen-De Vries syndrome | (Orphanet:96169) |
Leprechaunism | (Orphanet:508) |
Lethal congenital contracture syndrome type 2 | (Orphanet:137776) |
Lethal osteosclerotic bone dysplasia | (Orphanet:1832) |
MICROPHTHALMIA, SYNDROMIC 9 | (OMIM:601186) |
Matthew-Wood syndrome | (Orphanet:2470) |
McKusick-Kaufman syndrome | (Orphanet:2473) |
Megacystis-microcolon-intestinal hypoperistalsis syndrome | (Orphanet:2241) |
Mesomelia-synostoses syndrome | (Orphanet:2496) |
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency | (Orphanet:1194) |
Mowat-Wilson syndrome | (Orphanet:2152) |
Mullerian derivatives - lymphangiectasia - polydactyly | (Orphanet:1655) |
Multicystic renal dysplasia | (Orphanet:1851) |
Multiple congenital anomalies - hypotonia - seizures syndrome | (Orphanet:280633) |
NODULI CUTANEI, MULTIPLE, WITH URINARY TRACT ABNORMALITIES | (OMIM:163850) |
Neonatal hemochromatosis | (Orphanet:446) |
Nijmegen breakage syndrome | (Orphanet:647) |
Noonan syndrome | (Orphanet:648) |
OSTEOGENESIS IMPERFECTA, TYPE VII | (OMIM:610682) |
Occipital horn syndrome | (Orphanet:198) |
Ochoa syndrome | (Orphanet:2704) |
Okihiro syndrome | (Orphanet:93293) |
Osteodysplasty, Melnick-Needles type | (Orphanet:2484) |
Otopalatodigital syndrome | (Orphanet:669) |
Otopalatodigital syndrome type 2 | (Orphanet:90652) |
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER) | (OMIM:214100) |
PRUNE BELLY SYNDROME WITH PULMONIC STENOSIS, MENTAL RETARDATION, ANDDEAFNESS | (OMIM:264140) |
Pelviscapular dysplasia | (Orphanet:93333) |
Peters-plus syndrome | (Orphanet:709) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Prominent glabella - microcephaly - hypogenitalism | (Orphanet:2083) |
Prune belly syndrome | (Orphanet:2970) |
Rabson-Mendenhall syndrome | (Orphanet:769) |
Recombinant 8 syndrome | (Orphanet:96167) |
Schinzel-Giedion syndrome | (Orphanet:798) |
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) |
TARP syndrome | (Orphanet:2886) |
UROFACIAL SYNDROME 1 | (OMIM:236730) |
UROFACIAL SYNDROME 2 | (OMIM:615112) |
VACTERL ASSOCIATION, X-LINKED, WITH OR WITHOUT HYDROCEPHALUS | (OMIM:314390) |
VACTERL/VATER association | (Orphanet:887) |
VESICOURETERAL REFLUX 3 | (OMIM:613674) |
WEBB-DATTANI SYNDROME | (OMIM:615926) |
WEYERS ULNAR RAY/OLIGODACTYLY SYNDROME | (OMIM:602418) |
Wolfram syndrome 1 | (OMIM:222300) |
Wolfram syndrome, mitochondrial form | (OMIM:598500) |
X-linked dominant chondrodysplasia punctata | (Orphanet:35173) |
Xanthinuria type I | (Orphanet:93601) |
Zellweger syndrome | (Orphanet:912) |
Zunich-Kaye syndrome | (Orphanet:3474) |