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Ontology Browser

Term:
autosomal dominant progressive nephropathy with hypertension (EFO:MONDO:0008071)
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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 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:88659 ;   http://identifiers.org/medgen/98012 ;   http://identifiers.org/mesh/C562889 ;   http://identifiers.org/snomedct/703310005 ;   http://linkedlifedata.com/resource/umls/id/C0403443 ;   http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/1997246041 ;   https://omim.org/entry/161900 ;   nephropathy-hypertension
Related Synonyms: RFH1 ;   nephritis, familial, without deafness or ocular defect ;   nephropathy, familial ;   renal failure, adult-onset ;   renal failure, progressive, with hypertension
Alternate IDs: MONDO:0008071
Xrefs: GARD:16772 ;   ICD9:583.9 ;   MEDGEN:98012 ;   MESH:C562889 ;   MIM:161900 ;   ORDO:88659 ;   SCTID:703310005 ;   UMLS:C0403443 ;   icd11.foundation:1997246041

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