MSeqDR Mitochondrial Disease Portal


 
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Parent Node:
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kidney disease (MONDO:0005240)
..Starting node
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anuria ()

       Child Nodes:



 Sister Nodes: 
..expandAlsing syndrome ()
..expandanuria ()
..expandArnold stickler bourne syndrome ()
..expandatheroembolism of kidney ()
..expandC1q nephropathy ()
..expandchronic kidney disease ()
..expandcongenital anomaly of kidney and urinary tract ()
..expandcrush syndrome ()
..expandcystic kidney disease ()
..expanddiabetes insipidus ()
..expandfamilial juvenile hyperuricemic nephropathy ()
..expandglomerular disease ()
..expandhantavirus hemorrhagic fever with renal syndrome ()
..expandhematological disorder with renal involvement ()
..expandhydronephrosis ()
..expandhypertensive renal disease ()
..expandimpaired renal function disease ()
..expandinherited renal cancer-predisposing syndrome ()
..expandkidney cortex necrosis ()
..expandkidney failure ()
..expandkidney hypertrophy ()
..expandkidney neoplasm ()
..expandkidney papillary necrosis ()
..expandlachiewicz sibley syndrome ()
..expandnephritis ()
..expandnephrocalcinosis ()
..expandnephrolithiasis ()
..expandnephropathy secondary to a storage or other metabolic disease ()
..expandnephropathy-associated ciliopathy ()
..expandnephrosis ()
..expandobstructive nephropathy ()
..expandorthostatic proteinuria ()
..expandperinephritis ()
..expandproteinuria ()
..expandpyonephrosis ()
..expandrare cause of hypertension ()
..expandrare renal tubular disease ()
..expandrenal aminoaciduria ()
..expandrenal artery disease ()
..expandrenal disease with cataract ()
..expandrenal hypertension ()
..expandrenal infectious disease ()
..expandrenal tuberculosis ()
..expandrenal tubule disease ()
..expandstricture or kinking of ureter ()
..expandthrombotic microangiopathy ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:2476
Name:anuria
Definition:Absence of urine output.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:suppression of urinary secretion
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
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