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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
17q11 microdeletion syndrome 
Acute hepatic porphyria +  
adenovirus renal infection 
Adult familial nephronophthisis - spastic quadriparesia 
Alpha-1-antitrypsin deficiency 
anuria 
atheroembolism of kidney 
Autosomal dominant medullary cystic kidney disease with hyperuricemia 
Autosomal dominant polycystic kidney disease +  
autosomal dominant progressive nephropathy with hypertension 
Autosomal recessive infantile hypercalcemia 
Behcet's syndrome  
Brachydactyly - arterial hypertension 
Cerebro-reno-digital syndrome 
chronic kidney disease +   
Congenital disorder of glycosylation with nephropathy as a major feature 
Congenital erythropoietic porphyria 
congenital primary megaureter +  
cystic kidney disease +   
diabetes insipidus +  
duplication of urethra 
exstrophy-epispadias complex +   
Familial porphyria cutanea tarda +  
fetal lower urinary tract obstruction +   
Genetic glomerular disease +  
Genetic renal or urinary tract malformation +  
Genetic renal tubular disease +  
Genetic thrombotic microangiopathy 
glomerular disease +   
Glycogen storage disease due to glucose-6-phosphatase deficiency +  
Gräsbeck-Imerslund disease 
hantavirus hemorrhagic fever with renal syndrome +  
Hematological disorder with renal involvement +  
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 cataract - microcornea - renal glucosuria 
Juvenile nephronophthisis 
Juvenile nephropathic cystinosis 
kidney cortex necrosis 
kidney failure +   
kidney neoplasm +   
kidney papillary necrosis +  
nephritis +   
nephrocalcinosis +  
nephrolithiasis +   
nephrosis +   
Neurofibromatosis type 1 due to NF1mutation or intragenic deletion 
perinephritis 
polymyositis +   
post-operative acute kidney injury  
Proximal tubulopathy - diabetes mellitus - cerebellar ataxia 
Pseudoxanthoma elasticum 
renal aminoaciduria 
renal artery disease +  
renal dysplasia +  
Renal glucosuria 
renal glycosuria 
renal hypertension +  
renal hypoplasia +  
renal nutcracker syndrome 
renal tuberculosis +  
renal tubular dysgenesis +  
renal tubular transport disease +  
renal tubule disease +  
sialidosis type II +  
stricture or kinking of ureter  
systemic lupus erythematosus +   
systemic scleroderma +   
Takayasu arteritis  
temporal arteritis  
Tyrosinemia type 1 
ureteral disorder +   
Vitamin B12-responsive methylmalonic acidemia type cblA 
Vitamin B12-responsive methylmalonic acidemia type cblB 
X-linked diffuse leiomyomatosis-Alport syndrome 
X-linked erythropoietic protoporphyria 
Zellweger syndrome 

Synonyms
Exact Synonyms: Autosomal recessive infantile NPHP ;   Autosomal recessive infantile nephronophthisis
Xrefs: ICD10:Q61.5
External Ontologys: has_disease_location EFO:UBERON:0002113

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