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Parent Node:
expandFanconi syndrome (MONDO:0001083)
Parent Node:
expandinherited renal tubular disease (MONDO:0015962)
..Starting node
..expandprimary Fanconi syndrome ()

       Child Nodes:
........expandFanconi renotubular syndrome 2 ()
........expandFanconi renotubular syndrome 3 ()
........expandFRTS1 ()



 Sister 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 ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:7600
Name:primary Fanconi syndrome
Definition:Fanconi syndrome is a condition in which the kidneys do not absorb certain substances into the body. These substances, such as cysteine , fructose , galactose , or glycogen , are lost in the urine. Fanconi syndrome is thought to be caused by genetic and environmental factors, and it may be diagnosed at any age. Symptoms of Fanconi syndrome include increased urine production (which may cause dehydration ), weakness, and abnormalities of the bones.
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Synonyms:Fanconi renotubular syndrome 1; FRTS1; primary Fanconi renotubular syndrome
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Reference: MedGen:
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