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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
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  
central nervous system AIDS arteritis 
cerebral arteritis 
Cerebro-reno-digital syndrome 
chronic kidney disease +   
Churg-Strauss syndrome  
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  
primary central nervous system vasculitis 
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  
A large vessel vasculitis predominantly involving the arteries originating from the aortic arch and especially the extracranial branches of the carotid arteries. A systemic autoimmune disorder that typically affects medium and large ARTERIES, usually leading to occlusive granulomatous vasculitis with transmural infiltrate containing multinucleated GIANT CELLS. The TEMPORAL ARTERY is commonly involved. This disorder appears primarily in people over the age of 50. Symptoms include FEVER; FATIGUE; HEADACHE; visual impairment; pain in the jaw and tongue; and aggravation of pain by cold temperatures. (From Adams et al., Principles of Neurology, 6th ed)
ureteral disorder +   
X-linked diffuse leiomyomatosis-Alport syndrome 

Synonyms
Exact Synonyms: DOID:13375 ;   Giant Cell Arteritis ;   Giant cell arteritis (disorder) ;   Giant cell arteritis NOS (disorder) ;   Horton disease ;   NCIT:C35065 ;   Orphanet:397 ;   Temporal arteritis (disorder) ;   http://identifiers.org/medgen/365495 ;   http://identifiers.org/snomedct/400130008
Synonyms: http://identifiers.org/meddra/10018250 ;   http://identifiers.org/meddra/10043207
Related Synonyms: GCA ;   Horton's arteritis ;   Horton's giant cell arteritis ;   Horton's temporal arteritis ;   Horton’s disease ;   Horton’s syndrome ;   arteritis cranialis ;   arteritis temporalis ;   cranial arteritis ;   polymyalgia rheumatica
Xrefs: DOID:13375 ;   GARD:9615 ;   ICD10:M31.6 ;   ICD9:446.5 ;   MEDGEN:365495 ;   MIM:187360 ;   MONDO:0008538 ;   MeSH:D013700 ;   MedDRA:10018250 ;   MedDRA:10043207
External Ontologys: disease_has_inflammation_site EFO:UBERON:0001632
Definition Sources: https://orcid.org/0000-0001-5208-3432, Orphanet:397

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