Hereditary fructose intolerance

Hereditary fructose intolerance (HFI) is an autosomal recessive disorder of fructose metabolism, resulting from a deficiency of hepatic fructose-1-phosphate aldolase activity and leading to gastrointestinal disorders and postprandial hypoglycemia following fructose ingestion. HFI is a benign condition when treated, but it is life-threatening and potentially fatal if left untreated.

Also known as: Fructosaemia, Fructose Intolerance, Hereditary, fructose intolerance, fructose intolerance, hereditary, fructose-1,6-bisphosphate aldolase B deficiency, fructosemia, hereditary fructose intolerance, hereditary fructose intolerance syndrome

1 clinical trial for this condition and its sub-types.