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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
autosomal recessive cutis laxa type IC  
bacteriuria  
bladder disease +   
CAKUT +   
congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay  
kidney disease +   
A urinary system disease that is located_in the kidney. (DO)
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 +   
 anuria +   
 CAKUT1  
 hydronephrosis +   
 Hyperoxaluria +   
 kidney failure +   
 nephritis +   
 nephrolithiasis +   
 nephrosclerosis +   
 proteinuria +   
 pyelitis +   
 renal agenesis +   
 renal fibrosis +   
 uremia +   

Synonyms
Exact Synonyms: impaired renal function disease ;   kidney diseases ;   nephropathy ;   renal disease
Narrow Synonyms: RENAL DYSPLASIA ;   kidney injury
Primary IDs: MESH:D007674
Alternate IDs: DOID:11705 ;   MIM:602914 ;   OMIA:000710
Xrefs: EFO:0003086 ;   EFO:0009833 ;   ICD10CM:N08 ;   NCI:C3149 ;   NCI:C34843
Definition Sources: http://www.nlm.nih.gov/medlineplus/kidneydiseases.html "DO" "DO"

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