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Ontology Browser
Term:
fetal lower urinary tract obstruction (EFO:MONDO:0018559)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0) Pig: (0) Naked Mole-rat: (0) Green Monkey: (0)
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  
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: LUTO ;   Orphanet:435365 ;   http://identifiers.org/medgen/931214 ;   http://identifiers.org/snomedct/717752005 ;   http://linkedlifedata.com/resource/umls/id/C4305545 ;   http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/1661120971
Alternate IDs: MONDO:0018559
Xrefs: GARD:21804 ;   MEDGEN:931214 ;   ORDO:435365 ;   SCTID:717752005 ;   UMLS:C4305545 ;   icd11.foundation:1661120971

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