Hydronephrosis

Symptom Information:

Symptom ID: HPO:0000126
Synonyms:
Hydronephrosis (disorder) [Orphanet:37720]
Ureterohydronephrosis [Orphanet:37720]
Hydronephrosis [Orphanet:37720]
Hydronephrosis [OMIM:Hydronephrosis]
Megaureter/hydronephrosis/pyeloureteral junction syndrome [Orphanet:37720]
Hydronephrosis [MedDRA:10020524]
Bilateral hydronephrosis [MedDRA:10020524]
Ureterohydronephrosis [MedDRA:10020524]
Hydronephrosis (1 patient) [OMIM:Hydronephrosis (1 patient)]
Hydronephrosis (in some patients) [OMIM:Hydronephrosis (in some patients)]
Hydronephrosis (male) [OMIM:Hydronephrosis (male)]
Hydronephrosis (rare) [OMIM:Hydronephrosis (rare)]
Hydronephrosis (secondary to ureteral compression from hydrometrocolpos) [OMIM:Hydronephrosis (secondary to ureteral compression from hydrometrocolpos)]
Hydronephrosis, bilateral [OMIM:Hydronephrosis, bilateral]
Quality:
Cross references:
Orphanet:37720 "Megaureter/hydronephrosis/pyeloureteral junction syndrome" [Orphanet:37720]
OMIM: "Hydronephrosis" [OMIM:Hydronephrosis]
OMIM: "Hydronephrosis (1 patient)" [OMIM:Hydronephrosis (1 patient)]
OMIM: "Hydronephrosis (in some patients)" [OMIM:Hydronephrosis (in some patients)]
OMIM: "Hydronephrosis (male)" [OMIM:Hydronephrosis (male)]
OMIM: "Hydronephrosis (rare)" [OMIM:Hydronephrosis (rare)]
OMIM: "Hydronephrosis (secondary to ureteral compression from hydrometrocolpos)" [OMIM:Hydronephrosis (secondary to ureteral compression from hydrometrocolpos)]
OMIM: "Hydronephrosis, bilateral" [OMIM:Hydronephrosis, bilateral]
UMLS:C0020295 "Hydronephrosis" [HPO:0000126]
UMLS:C1168284 "Ureterohydronephrosis" [Orphanet:37720]
UMLS:C0020295 "Hydronephrosis" [Orphanet:37720]
Is a (Direct Parents):
Orphanet Hydroureter
MedDRA Renal obstructive disorders
Orphanet Bladder and ureter anomalies
HPO         Dilatation of the renal pelvis
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)
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)