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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
bladder disease +   
congenital urachal anomaly +  
Congenital urachal anomaly (CUA) describes a group of urachal remnants, found more frequently in males than females, that result from incomplete closure of the urachus (an embryological remnant of the allantois) during prenatal development, and that are usually asymptomatic (and found as an incidental finding on a radiological study) but can also present with umbilical discharge (in patent urachus or urachal sinus), infraumblical mass and pain, or with complications such as obstruction and infection. CUAs include patent urachus, urachal sinus, urachal cyst and urachal diverticulum.
kidney disease +   
nephrotoxicity 
paraneoplastic renal syndrome 
Rare genetic renal disease +  
ureteral disorder +   
urethral disease +  
urinary system neoplasm +   
urinary tract infection +   
urinary tract obstruction +  
urolithiasis +   
urothelial hyperplasia +  

Synonyms
Alternate IDs: MONDO:0018565
Xrefs: GARD:21814 ;   MEDGEN:1433102 ;   ORDO:435743 ;   UMLS:C1739100
Definition Sources: Orphanet:435743

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