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:
expandrenal tubule disease (MONDO:0021568)
..Starting node
..expandinherited renal tubular disease ()

       Child Nodes:
........expandAlstrom syndrome ()
........expandBartter syndrome ()
........expandcranioectodermal dysplasia ()
........expandcystinuria (disease) ()
........expandDent disease ()
........expanddominant hypophosphatemia with nephrolithiasis or osteoporosis ()
........expandEAST syndrome ()
........expandfamilial juvenile hyperuricemic nephropathy type 2 ()
........expandfamilial primary hypomagnesemia ()
........expandGitelman syndrome ()
........expandhereditary renal hypouricemia ()
........expandhyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome ()
........expandhypotonia-cystinuria syndrome type 1 ()
........expandidiopathic inherited hypercalciuria ()
........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 Fanconi syndrome ()
........expandprimary renal tubular acidosis ()
........expandpseudohypoaldosteronism type 1 ()
........expandpseudohypoparathyroidism ()
........expandpsychomotor regression-oculomotor apraxia-movement disorder-nephropathy syndrome ()
........expandRHYNS syndrome ()
........expandSenior-Boichis syndrome ()
........expandSenior-Loken syndrome ()



 Sister Nodes: 
..expandFanconi syndrome ()
..expandinherited renal tubular disease ()
..expandmucinous tubular and spindle renal cell carcinoma ()
..expandrenal tubular acidosis ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:15962
Name:inherited renal tubular disease
Definition:
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:genetic renal tubular disease
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal