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 tubular transport disease (MONDO:0006510)
Parent Node:
expandrenal tubule disease (MONDO:0021568)
Parent Node:
expandsyndromic disease (MONDO:0002254)
..Starting node
..expandFanconi syndrome ()

       Child Nodes:
........expandacquired Fanconi syndrome ()
........expandadult Fanconi syndrome ()
........expanddeal barratt dillon syndrome ()
........expandFanconi renotubular syndrome 4 with maturity-onset diabetes of the young ()
........expandprimary Fanconi syndrome ()



 Sister Nodes: 
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..expanddiffuse infiltrative lymphocytosis syndrome ()
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..expandDuane retraction syndrome ()
..expanddumping syndrome ()
..expandempty sella syndrome ()
..expandeuthyroid sick syndrome ()
..expandFanconi syndrome ()
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..expandLown-Ganong-Levine syndrome ()
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..expandsick sinus syndrome ()
..expandsubclavian steal syndrome ()
..expandsubstance withdrawal syndrome ()
..expandsuperior mesenteric artery syndrome ()
..expandsyndromic intellectual disability ()
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..expandtethered spinal cord syndrome ()
..expandthoracic outlet syndrome ()
..expandTietze syndrome ()
..expandtoxic shock syndrome ()
..expandvertebral artery insufficiency ()
..expandWaterhouse-Friderichsen syndrome ()
..expandWissler syndrome ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:1083
Name:Fanconi syndrome
Definition:A genetic or acquired disorder characterized by impairment of the function of the proximal tubules of the kidney. It results in decreased reabsorption of electrolytes, glucose, amino acids, and other nutrients.
Alternative IDs:
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TreeNumbers:
Synonyms:adult Fanconi syndrome; congenital Fanconi syndrome; De toni-debre-Fanconi syndrome; De toni-Fanconi syndrome; deToni Fanconi syndrome; Fanconi renotubular syndrome; Fanconi syndrome; Fanconi's syndrome; Fanconi-de toni syndrome; Fanconi-de-toni syndrome; infantile nephropathic cystinosis; Lignac-Fa
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
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