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Iron overloadTyrosinemia type iLipoprotein lipase deficiencyFamilial adenomatous polyposisGlycogen storage disease type iGlycogen storage disease type iiiFamilial hypercholesterolemiaHereditary elliptocytosisCystinuriaGaucher's diseaseBiotinidase deficiencyIschemic colitisCoeliac diseaseHemolytic jaundiceMethylmalonic acidemiaHemosiderosisEncapsulating peritoneal sclerosisAceruloplasminemiaAbetalipoproteinemiaDiabetesHomocystinuriaPernicious anemiaHemolytic anemiaAlkaptonuriaHaemophiliaRefsum diseaseHemoglobinemiaBlind loop syndromeFructose malabsorptionHurler syndromeGlycogen storage diseaseHistamine intoleranceSevere combined immunodeficiencyDiverticulitisMenkes diseaseLysosomal acid lipase deficiencyBile acid malabsorptionGalactosemiaBowel obstructionGlycogen storage disease type iiHemoglobinopathySerrated polyposis syndromeCitrullinemiaIntestinal pseudo-obstructionI-cell diseaseGlycogen storage disease type vNon-alcoholic fatty liver diseaseHunter syndromeFamilial dysbetalipoproteinemiaMyeloperoxidase deficiencyNeurofibromatosis type iAcute intermittent porphyriaType 2 diabetesMetabolic disorderGastroesophageal reflux diseaseRenal tubular acidosisSteatohepatitisCaroli diseaseHaemophilia aGitelman syndromeCirrhosisHyperhomocysteinemiaFumarase deficiencyMorquio syndromeHereditary fructose intoleranceAutoimmune hemolytic anemiaAtrophic gastritisPneumatosis intestinalisMucolipidosisHereditary spherocytosisGardner's syndromeAutoimmune hepatitisHemophagocytic lymphohistiocytosisEvans syndromeHypophosphatasiaPrimary hyperoxaluriaCystinosisHartnup diseaseMonoclonal gammopathyChronic liver diseasePortal hypertensionAbdominal obesityProthrombin g20210aPortal vein thrombosisChronic mountain sicknessBiliary dyskinesiaRotor syndromePyruvate kinase deficiencyHaemophilia bIschemic hepatitisHemoglobinuriaAlcoholic liver diseaseLupusPrimary sclerosing cholangitisAcdcMalabsorptionFatty liver diseaseIron poisoningDuodenal lymphocytosisGastrointestinal bleeding