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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
kidney disease +     
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 dysgenesis is a rare disorder of the fetus characterized by absent or poorly developed proximal tubules of the kidneys, persistent oligohydramnios, leading to Potter sequence (facial dysmorphism with large and flat low-set ears, lung hypoplasia arthrogryposis and limb positioning defects), and skull ossification defects. It can be acquired during fetal development due to drugs taken by the mother or certain disorders (twin-twin transfusion syndrome, TTTS) or inherited in an autosomal recessive manner.
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: Orphanet:3033 ;   http://identifiers.org/medgen/82738 ;   http://identifiers.org/snomedct/702397002 ;   http://linkedlifedata.com/resource/umls/id/C0266313 ;   http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/191424358 ;   primitive renal tubule syndrome ;   renotubular dysgenesis
Alternate IDs: MONDO:0017609
Xrefs: GARD:379 ;   MEDGEN:82738 ;   ORDO:3033 ;   SCTID:702397002 ;   UMLS:C0266313 ;   icd11.foundation:191424358
Definition Sources: Orphanet:3033

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