Ureteral stenosis

Symptom Information:

Symptom ID: HPO:0000071
Synonyms:
Ureter stenosis [Orphanet:37680]
Stricture of ureter (disorder) [Orphanet:37680]
Stenosis of ureter (disorder) [Orphanet:37680]
Stenosis of ureter [Orphanet:37680]
Ureteral stenosis [OMIM:Ureteral stenosis]
Ureteral stenosis/narrowing [Orphanet:37680]
Ureteric stenosis [Orphanet:37680]
Ureteric stenosis [MedDRA:10046411]
Kinking of ureter [MedDRA:10046411]
Stenosis ureteral [MedDRA:10046411]
Stricture of pelviureteric juncture [MedDRA:10046411]
Stricture or kinking of ureter [MedDRA:10046411]
Ureteral stricture [MedDRA:10046411]
Quality:
Cross references:
Orphanet:37680 "Ureteral stenosis/narrowing" [Orphanet:37680]
OMIM: "Ureteral stenosis" [OMIM:Ureteral stenosis]
UMLS:C0521618 "Stenosis of ureter" [Orphanet:37680]
Is a (Direct Parents):
HPO         Ureteral obstruction
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)
                   Ureteral obstruction(HPO:0006000)
                      Ureteral stenosis(HPO:0000071)
MedDRA:
Renal and urinary disorders(MedDRA:10038359)
    Ureteric disorders(MedDRA:10046400)
       Ureteric disorders NEC(MedDRA:10046402)
          Ureteral stenosis(HPO:0000071)
Database Frequency: 9 / 7739
Resource:

All diseases associated with this symptom:

Cholestasis - pigmentary retinopathy - cleft palate (Orphanet:1415)
Dystrophic epidermolysis bullosa (Orphanet:303)
Frontometaphyseal dysplasia (Orphanet:1826)
Granulomatosis with polyangiitis (Orphanet:900)
Junctional epidermolysis bullosa - pyloric atresia (Orphanet:79403)
Oculocerebral hypopigmentation syndrome, Cross type (Orphanet:2719)
Osteodysplasty, Melnick-Needles type (Orphanet:2484)
Polyarteritis nodosa (Orphanet:767)
Schinzel-Giedion syndrome (Orphanet:798)