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hereditary fructose intolerance

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Mondo Description 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.
Uniprot Description Autosomal recessive disease that results in an inability to metabolize fructose and related sugars. Complete exclusion of fructose results in dramatic recovery; however, if not treated properly, HFI subjects suffer episodes of hypoglycemia, general ill condition, and risk of death the remainder of life.
Mondo Term and Equivalent IDs
MONDO:0009249:  hereditary fructose intolerance
GARD:0006622: 
ICD10:E74.12: 
NCIT:C84720: 
Orphanet:469: 
SCTID:20052008: 
UMLS:C0016751: