Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources
Advanced Search (OLGA)

Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
bladder disease +   
congenital urachal anomaly +  
kidney disease +   
A disease affecting the kidneys A disease involving the kidney.
nephrotoxicity 
paraneoplastic renal syndrome 
Rare genetic renal disease +  
ureteral disorder +   
urethral disease +  
urinary system neoplasm +   
urinary tract infection +   
urinary tract obstruction +  
urolithiasis +   
urothelial hyperplasia +  
 adenovirus renal infection 
 Adult familial nephronophthisis - spastic quadriparesia 
 anuria 
 atheroembolism of kidney 
 Autosomal dominant medullary cystic kidney disease with hyperuricemia 
 autosomal dominant progressive nephropathy with hypertension 
 Behcet's syndrome  
 Cerebro-reno-digital syndrome 
 chronic kidney disease +   
 congenital primary megaureter +  
 cystic kidney disease +  
 diabetes insipidus +  
 duplication of urethra 
 exstrophy-epispadias complex +   
 fetal lower urinary tract obstruction +   
 glomerular disease +   
 hantavirus hemorrhagic fever with renal syndrome +  
 hemoglobinuria +  
 hemorrhagic fever with renal syndrome 
 Hepatic fibrosis - renal cysts - intellectual disability 
 hydronephrosis +  
 hypertensive nephropathy +   
 impaired renal function disease +  
 Infantile nephronophthisis 
 inherited kidney disorder +   
 Juvenile nephronophthisis 
 kidney cortex necrosis 
 kidney failure +  
 kidney neoplasm +   
 kidney papillary necrosis +  
 nephritis +   
 nephrocalcinosis +  
 nephrolithiasis +   
 nephrosis +   
 perinephritis 
 polymyositis +   
 post-operative acute kidney injury  
 renal aminoaciduria 
 renal artery disease +  
 renal dysplasia +  
 renal glycosuria 
 renal hypertension +  
 renal hypoplasia +  
 renal nutcracker syndrome 
 renal tuberculosis +  
 renal tubular dysgenesis +  
 renal tubular transport disease +  
 renal tubule disease +  
 stricture or kinking of ureter 
 systemic lupus erythematosus +   
 systemic scleroderma +   
 Takayasu arteritis  
 temporal arteritis  
 ureteral disorder +   
 X-linked diffuse leiomyomatosis-Alport syndrome 

Synonyms
Exact Synonyms: DOID:557 ;   Kidney Disorder ;   NCIT:C3149 ;   disease of kidney ;   disease or disorder of kidney ;   disorder of kidney ;   http://identifiers.org/medgen/9635 ;   http://identifiers.org/mesh/D007674 ;   http://identifiers.org/snomedct/90708001 ;   http://linkedlifedata.com/resource/umls/id/C0022658
Related Synonyms: nephropathy
Xrefs: DOID:557 ;   HP:0000077 ;   HP:0000112 ;   ICD10:N01 ;   ICD10:N26 ;   ICD9:583.81 ;   MEDGEN:9635 ;   MESH:D007674 ;   MONDO:0005240 ;   MedDRA:10051051
External Ontologys: disease_has_location EFO:UBERON:0002113
Definition Sources: https://orcid.org/0000-0002-6601-2165

paths to the root