Duplicated collecting system
Symptom Information:
Symptom ID: | HPO:0000081 | ||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |