Congenital megaureter

Symptom Information:

Symptom ID: HPO:0008676
Synonyms:
Congenital megaloureter [HPO:0008676]
Congenital megaloureters [OMIM:Congenital megaloureters]
Quality:
Cross references:
OMIM: "Congenital megaloureters" [OMIM:Congenital megaloureters]
Is a (Direct Parents):
HPO         Abnormality of the ureter
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)
                   Congenital megaureter(HPO:0008676)
MedDRA:
Database Frequency: 3 / 7739
Resource:

All diseases associated with this symptom:

Beckwith-Wiedemann syndrome due to 11p15 microdeletion (Orphanet:231127)
Bilateral multicystic renal dysplasia (Orphanet:97364)
Multicystic renal dysplasia (Orphanet:1851)