DISEASES

Disease-gene associations mined from literature

Human genes for Fanconi syndrome

Fanconi syndrome [DOID:1062]

A renal tubular transport disease of the proximal renal tubes characterized by glucosuria, phosphaturia, generalized aminoaciduria and HCO3 wasting.

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

Linkouts:  OMIM #1 #2