Ureteral duplication

Symptom Information:

Symptom ID: HPO:0000073
Synonyms:
Double ureter [HPO:0000073]
Ureter duplication [Orphanet:37440]
Double ureter (disorder) [Orphanet:37440]
Double ureter [Orphanet:37440]
Double ureter [OMIM:Double ureter]
Ureteral duplication [OMIM:Ureteral duplication]
Ureter/calyx/pelvis duplication/bifid/retrocava/retroiliac ureter [Orphanet:37440]
Double ureter [MedDRA:10013613]
Duplex ureter [MedDRA:10013613]
Ureter double [MedDRA:10013613]
Double ureters [OMIM:Double ureters]
Retroiliac ureter [Orphanet:37440]
Renal calyx duplication [Orphanet:37440]
Retrocaval ureter [Orphanet:37440]
Retrocaval ureter (disorder) [Orphanet:37440]
Quality:
Cross references:
Orphanet:37440 "Ureter/calyx/pelvis duplication/bifid/retrocava/retroiliac ureter" [Orphanet:37440]
OMIM: "Double ureter" [OMIM:Double ureter]
OMIM: "Ureteral duplication" [OMIM:Ureteral duplication]
OMIM: "Double ureters" [OMIM:Double ureters]
UMLS:C0221365 "Double ureter" [Orphanet:37440]
UMLS:C0238495 "Retrocaval ureter" [Orphanet:37440]
Is a (Direct Parents):
HPO         Bifid ureter
HPO         Abnormality of the ureter
MedDRA Ureteric disorders congenital
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 duplication(HPO:0000073)
MedDRA:
Renal and urinary disorders(MedDRA:10038359)
    Ureteric disorders(MedDRA:10046400)
       Ureteric disorders congenital(MedDRA:10046401)
          Ureteral duplication(HPO:0000073)
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

AREDYLD syndrome (Orphanet:1133)
Carnitine palmitoyl transferase II deficiency, neonatal form (Orphanet:228308)
Caudal duplication (Orphanet:1756)
Congenital sodium diarrhea (Orphanet:103908)
Focal dermal hypoplasia (Orphanet:2092)
Fryns syndrome (Orphanet:2059)
Lethal restrictive dermopathy (Orphanet:1662)
MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,AND PSYCHOMOTOR DELAY (OMIM:601347)
Peters-plus syndrome (Orphanet:709)
URETER, BIFID OR DOUBLE (OMIM:191550)
VENTRICULOMEGALY WITH DEFECTS OF THE RADIUS AND KIDNEY (OMIM:602200)