Ureteropelvic junction obstruction

Symptom Information:

Symptom ID: HPO:0000074
Synonyms:
Pelviureteric junction obstruction [HPO:0000074]
Pelviureteric junction obstruction [Orphanet:37720]
Obstruction of pelviureteric junction (disorder) [Orphanet:37720]
Obstruction of pelviureteric junction [Orphanet:37720]
Pelviureteric junction obstruction [OMIM:Pelviureteric junction obstruction]
Ureteropelvic junction obstruction [OMIM:Ureteropelvic junction obstruction]
Megaureter/hydronephrosis/pyeloureteral junction syndrome [Orphanet:37720]
Pelvi-ureteric obstruction [Orphanet:37720]
Pelvi-ureteric obstruction [MedDRA:10034232]
Ureteropelvic junction obstruction [MedDRA:10034232]
Quality:
Cross references:
Orphanet:37720 "Megaureter/hydronephrosis/pyeloureteral junction syndrome" [Orphanet:37720]
OMIM: "Pelviureteric junction obstruction" [OMIM:Pelviureteric junction obstruction]
OMIM: "Ureteropelvic junction obstruction" [OMIM:Ureteropelvic junction obstruction]
UMLS:C0521619 "Obstruction of pelviureteric junction" [Orphanet:37720]
Is a (Direct Parents):
HPO         Ureteral stenosis
Orphanet Hydroureter
MedDRA Renal obstructive disorders
Orphanet Bladder and ureter anomalies
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)
                   Ureteral obstruction(HPO:0006000)
                      Ureteral stenosis(HPO:0000071)
                         Ureteropelvic junction obstruction(HPO:0000074)
MedDRA:
Renal and urinary disorders(MedDRA:10038359)
    Nephropathy(HPO:0000112)
       Renal obstructive disorders(MedDRA:10038488)
          Ureteropelvic junction obstruction(HPO:0000074)
Database Frequency: 15 / 7739
Resource:

All diseases associated with this symptom:

Bilateral multicystic renal dysplasia (Orphanet:97364)
CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT, SUSCEPTIBILITY TO (OMIM:610805)
DUAL SERINE/THREONINE AND TYROSINE PROTEIN KINASE (OMIM:612666)
Goldenhar syndrome (Orphanet:374)
Hand-foot-genital syndrome (Orphanet:2438)
KABUKI SYNDROME 1 (OMIM:147920)
Kabuki syndrome (Orphanet:2322)
Mowat-Wilson syndrome (Orphanet:2152)
Multicystic renal dysplasia (Orphanet:1851)
Rabson-Mendenhall syndrome (Orphanet:769)
Renal cysts and diabetes syndrome (Orphanet:93111)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Steinert myotonic dystrophy (Orphanet:273)
VACTERL/VATER association (Orphanet:887)
Zunich-Kaye syndrome (Orphanet:3474)