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:
expandkidney disease (MONDO:0005240)
..Starting node
..expandrare renal tubular disease ()

       Child Nodes:
........expandAlstrom syndrome ()
........expandcranioectodermal dysplasia ()
........expandcystinuria (disease) ()
........expanddominant hypophosphatemia with nephrolithiasis or osteoporosis ()
........expandEAST syndrome ()
........expandfamilial juvenile hyperuricemic nephropathy type 2 ()
........expandfamilial primary hypomagnesemia ()
........expandhereditary renal hypouricemia ()
........expandhyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome ()
........expandhypotonia-cystinuria syndrome type 1 ()
........expandidiopathic inherited hypercalciuria ()
........expandIgG4-related kidney disease ()
........expandJeune syndrome ()
........expandmitochondrial DNA depletion syndrome, hepatocerebrorenal form ()
........expandnephrogenic diabetes insipidus ()
........expandnephrogenic diabetes insipidus-intracranial calcification syndrome ()
........expandnephrogenic syndrome of inappropriate antidiuresis ()
........expandnephronophthisis (disease) ()
........expandoculocerebrorenal syndrome ()
........expandprimary renal tubular acidosis ()
........expandpseudohypoparathyroidism ()
........expandpsychomotor regression-oculomotor apraxia-movement disorder-nephropathy syndrome ()
........expandrenal tubular transport disease ()
........expandRHYNS syndrome ()
........expandSenior-Boichis syndrome ()
........expandSenior-Loken syndrome ()
........expandtubulointerstitial nephritis and uveitis 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:19744
Name:rare renal tubular disease
Definition:Any disease in which the causes of the disease is a perturbation of the renal tubule leading to its dysfunction.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:disease of renal tubule; renal tubule disease
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal