has material basis in germline mutation in ALDOB hereditary fructose intolerance https://github.com/monarch-initiative/mondo/issues/4985 https://www.malacards.org/card/fructose_intolerance_hereditary ICD10CM:E74.12 Fructosaemia SCTID:20052008 NANDO:2200531 OMIM:229600 fructose intolerance DOID:9869 fructose-1,6-bisphosphate aldolase B deficiency GARD:0006622 ICD9:271.2 fructosemia NCIT:C84720 icd11.foundation:1925240365 NORD:1166 hereditary fructosemia hereditary fructose-1-phosphate aldolase deficiency MEDGEN:42105 Orphanet:469 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. fructose intolerance, hereditary Fructose Intolerance, Hereditary hereditary fructose intolerance MedDRA:10019878 UMLS:C0016751 hereditary fructose intolerance syndrome obsolete congenital intestinal transport defect disorder of fructose metabolism disorder of carbohydrate transmembrane transport and absorption obsolete nephropathy secondary to a storage or other metabolic disease disorder of galactose and fructose metabolism