Disease-gene associations mined from literature

Human genes for Fanconi syndrome

Fanconi syndrome [DOID:1062]

Fanconi syndrome (also known as Fanconi's syndrome) is a disease of the proximal renal tubules of the kidney in which glucose, amino acids, uric acid, phosphate and bicarbonate are passed into the urine, instead of being reabsorbed. Fanconi syndrome affects the proximal tubule, which is the first part of the tubule to process fluid after it is filtered through the glomerulus. It may be inherited, or caused by drugs or heavy metals.

Synonyms:  Fanconi syndrome,  DOID:1062,  Fanconi disease,  Fanconi disorder,  Congenital Fanconi syndrome (disorder) ...

Linkouts:  OMIM #1 #2