Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

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)
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: 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", https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5468264/ "DO", https://www.ncbi.nlm.nih.gov/pubmed/25313840 "DO"

paths to the root

NHLBI Logo

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.