Duplicated collecting system

Symptom Information:

Symptom ID: HPO:0000081
Synonyms:
Double collecting system [HPO:0000081]
Double urinary collecting systems on intravenous pyelography [HPO:0000081]
Duplicated renal collecting system [HPO:0000081]
Double collecting system [OMIM:Double collecting system]
Double urinary collecting systems on intravenous pyelography [OMIM:Double urinary collecting systems on intravenous pyelography]
Duplicated collecting system [OMIM:Duplicated collecting system]
Duplicated renal collecting system [OMIM:Duplicated renal collecting system]
Duplicated collecting system (1 patient) [OMIM:Duplicated collecting system (1 patient)]
Quality:
Cross references:
OMIM: "Double collecting system" [OMIM:Double collecting system]
OMIM: "Double urinary collecting systems on intravenous pyelography" [OMIM:Double urinary collecting systems on intravenous pyelography]
OMIM: "Duplicated collecting system" [OMIM:Duplicated collecting system]
OMIM: "Duplicated renal collecting system" [OMIM:Duplicated renal collecting system]
OMIM: "Duplicated collecting system (1 patient)" [OMIM:Duplicated collecting system (1 patient)]
Is a (Direct Parents):
HPO         Ureteral duplication
HPO         Abnormality of the renal collecting system
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 collecting system(HPO:0004742)
                         Duplicated collecting system(HPO:0000081)
                Abnormality of the ureter(HPO:0000069)
                   Ureteral duplication(HPO:0000073)
                      Duplicated collecting system(HPO:0000081)
MedDRA:
Database Frequency: 16 / 7739
Resource:

All diseases associated with this symptom:

Cloacal exstrophy (Orphanet:93929)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1 (OMIM:129900)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 (OMIM:604292)
EEC syndrome (Orphanet:1896)
Exstrophy-epispadias complex (Orphanet:322)
FANCONI ANEMIA, COMPLEMENTATION GROUP A (OMIM:227650)
FANCONI ANEMIA, COMPLEMENTATION GROUP C (OMIM:227645)
FANCONI ANEMIA, COMPLEMENTATION GROUP D2 (OMIM:227646)
FANCONI ANEMIA, COMPLEMENTATION GROUP E (OMIM:600901)
Fanconi anemia (Orphanet:84)
Multiple congenital anomalies-hypotonia-seizures syndrome type 2 (Orphanet:300496)
NODULI CUTANEI, MULTIPLE, WITH URINARY TRACT ABNORMALITIES (OMIM:163850)
Renal cysts and diabetes syndrome (Orphanet:93111)
URETEROCELE (OMIM:191650)
VESICOURETERAL REFLUX 8 (OMIM:615963)
Zunich-Kaye syndrome (Orphanet:3474)