Hereditary fructose intolerance

MONDO:0009249

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

25 clinical trials for this condition and its sub-types.

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