MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, ND: NAMDC terms.
  Most Studied  CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO
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Parent Node:
expandkidney disease (MONDO:0005240)
..Starting node
..expandnephropathy secondary to a storage or other metabolic disease ()

       Child Nodes:
........expandadenine phosphoribosyltransferase deficiency ()
........expandalpha 1-antitrypsin deficiency ()
........expandamelogenesis imperfecta type 1G ()
........expandautosomal recessive infantile hypercalcemia ()
........expandcongenital disorder of glycosylation with nephropathy as a major feature ()
........expandFabry disease ()
........expandfamilial renal glucosuria ()
........expandgalactosemia ()
........expandglycogen storage disease due to GLUT2 deficiency ()
........expandglycogen storage disease I ()
........expandHartnup disease ()
........expandhereditary fructose intolerance ()
........expandhereditary xanthinuria ()
........expandhypoxanthine-guanine phosphoribosyltransferase deficiency ()
........expandImerslund-Grasbeck syndrome ()
........expandjuvenile cataract-microcornea-renal glucosuria syndrome ()
........expandjuvenile nephropathic cystinosis ()
........expandLCAT deficiency ()
........expandmethylmalonic aciduria due to methylmalonyl-CoA mutase deficiency ()
........expandnephropathic infantile cystinosis ()
........expandphosphoribosylpyrophosphate synthetase superactivity ()
........expandprimary hyperoxaluria ()
........expandproximal tubulopathy-diabetes mellitus-cerebellar ataxia syndrome ()  LSDB  L: 00144;
........expandsialidosis type 2 ()
........expandtyrosinemia type I ()
........expandvitamin B12-responsive methylmalonic acidemia ()
........expandWilson disease ()
........expandZellweger syndrome ()



 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:19743
Name:nephropathy secondary to a storage or other metabolic disease
Definition:
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
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