MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, ND: NAMDC terms.
  Most Studied  CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO
Disease Browser
Parent Node:
expanddevelopmental defect during embryogenesis (MONDO:0019755)
Parent Node:
expandkidney disease (MONDO:0005240)
..Starting node
..expandcongenital anomaly of kidney and urinary tract ()

       Child Nodes:
........expandbladder exstrophy-epispadias-cloacal exstrophy complex ()
........expandcongenital anomalies of kidney and urinary tract 1, susceptibility to ()
........expandcongenital anomalies of kidney and urinary tract type 2 ()
........expandfetal lower urinary tract obstruction ()
........expandnon-syndromic renal or urinary tract malformation ()
........expandsyndromic renal or urinary tract malformation ()



 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:19719
Name:congenital anomaly of kidney and urinary tract
Definition:A urinary system disease characterized by structural malformations in the kidney and/or urinary tract containing vesicoureteral reflux.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:CAKUT; congenital anomalies of kidney and urinary tract; congenital anomalies of the kidney and urinary tract; renal or urinary tract malformation
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal