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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
autosomal recessive cutis laxa type IC  
bacteriuria  
bladder disease +   
CAKUT +   
A urinary system disease characterized by structural malformations in the kidney and/or urinary tract containing vesicoureteral reflux. (DO)
congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay  
kidney disease +   
neonatal urinary tract infectious disease 
pyuria 
ureteral disease +   
urethral disease +   
urinary system benign neoplasm +   
urinary system cancer +   
urinary tract infection +   
urinary tract obstruction +   
Urination Disorders +   
urofacial syndrome +   
urolithiasis +   
Vesicoureteral Reflux 2  
Vesicoureteral Reflux 3  
Vesicoureteral Reflux 5  
Vesicoureteral Reflux 6 
Vesicoureteral Reflux 7 
Vesicoureteral Reflux 8  
X-Linked Vesicoureteral Reflux 

Synonyms
Exact Synonyms: NON-SYNDROMIC RENAL OR URINARY TRACT MALFORMATION ;   congenital anomalies of kidney and urinary tract ;   congenital anomalies of the kidney and urinary tract ;   renal or urinary tract malformation
Primary IDs: MESH:C566906
Xrefs: OMIM:PS610805 ;   ORDO:93545
Definition Sources: https://www.jci.org/articles/view/95300 "DO" "DO", https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5468264/ "DO" "DO", https://www.ncbi.nlm.nih.gov/pubmed/25313840 "DO" "DO"

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