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Ontology Browser

Parent Terms Term With Siblings Child Terms
autosomal recessive cutis laxa type IC  
bladder disease +   
A urinary system disease that is located_in the bladder. (DO)
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 +   
urofacial syndrome +   
urolithiasis +   

Exact Synonyms: bladder diseases ;   urinary bladder disease ;   urinary bladder diseases
Primary IDs: MESH:D001745
Xrefs: EFO:1000018 ;   ICD10CM:N32.9 ;   ICD9CM:596.9 ;   NCI:C2900
Definition Sources: "DO" "DO"

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