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Ontology Browser

Parent Terms Term With Siblings Child Terms
autosomal recessive cutis laxa type IC  
bladder disease +   
CAKUT +   
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 
ureteral disease +   
urethral disease +   
urinary system benign neoplasm +   
urinary system cancer +   
urinary tract infection +   
urinary tract obstruction +   
Urination Disorders +   
Abnormalities in the process of URINE voiding, including bladder control, frequency of URINATION, as well as the volume and composition of URINE.
urofacial syndrome +   
urolithiasis +   
 anuria +   
 Enuresis +   
 Glycosuria +   
 Hematuria +   
 Oliguria +   
 Polyuria +   
 proteinuria +   

Exact Synonyms: Urination Disorder
Primary IDs: MESH:D014555
Definition Sources: MESH:D014555

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