disease has basis in dysfunction of ALDOB hereditary fructose intolerance Aldob deficiency DOID:9869 Fructosaemia GARD:0006622 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. ICD10:E74.1 ICD10:E74.12 ICD9:271.2 MONDO:0009249 MedDRA:10019878 NCIT:C84720 OMIM:229600 Orphanet:469 SCTID:20052008 UMLS:C0016751 aldolase B deficiency fructose intolerance fructose intolerance, hereditary fructose-1,6-bisphosphate aldolase B deficiency fructose-1-phosphate aldolase deficiency fructosemia hereditary fructose intolerance syndrome hereditary fructose-1-phosphate aldolase deficiency hereditary fructosemia congenital intestinal transport defect metabolic disease with intestinal involvement disorder of fructose metabolism disorder of carbohydrate absorption and transport nephropathy secondary to a storage or other metabolic disease