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675 Possible Causes for Hereditary Fructose Intolerance

  • Hereditary Fructose Intolerance

    Hereditary fructose intolerance is a rare, but potentially lethal, inherited disorder of fructose metabolism, caused by mutation of the aldolase B gene.[ncbi.nlm.nih.gov] Chapter 9, Disorders of fructose metabolism; p. 157-165.[invitae.com] […] potentially lethal, inherited disorder of fructose metabolism, caused by mutation of the aldolase B gene.[link.springer.com]

  • Primary Hyperoxaluria

    fructose intolerance Inclusion body myopathy 2 Isovaleric acidemia Krabbe disease Leber congenital amaurosis 10 and other CEP290 -related ciliopathies Leber congenital amaurosis[sema4.com] ., elevated transaminase or hyperbilirubinemia levels) Hemochromatosis (1:300) α 1 -antitrypsin deficiency (1:8,000) Hereditary fructose intolerance (1:20,000 to 1:50,000)[aafp.org] Glycogen storage disease, type Ib Glycogen storage disease, type II Glycogen storage disease, type III GRACILE syndrome and other BCS1L -related disorders Hemoglobin C disease Hereditary[sema4.com]

  • Neonatal Hepatitis

    Metabolic etiologies include galactosemia, tyrosinemia, hereditary fructose intolerance, cytochrome chain defects, Zellweger syndrome, neonatal hemochromatosis, and alpha-one-antitrypsin[nature.com]

  • Hypophosphatemia

    FANCONI SYNDROME Congenital :Cystinosis, Wilson’s disease, hereditary fructose intolerance glycogen storage disease Acquired: Multiple myeloma, SLE, amyloidosis, antiretroviral[slideshare.net] In children, cystinosis, Wilson disease, and hereditary fructose intolerance are the most common of the syndrome.[emedicine.medscape.com]

  • Glycogen Storage Disease Type 2

    metabolism E74.10 Disorder of fructose metabolism, unspecified E74.12 Hereditary fructose intolerance E74.19 Other disorders of fructose metabolism E74.2 Disorders of galactose[icd10data.com] […] heterogeneous group caused by inability to metabolize specific… 1. galactosemia... 2. hereditary fructose intolerance... 3. frustose… hypoglycemia... hepatosplenomegaly...[quizlet.com] , unspecified E74 Other disorders of carbohydrate metabolism E74.0 Glycogen storage disease E74.02 Pompe disease E74.09 Other glycogen storage disease E74.1 Disorders of fructose[icd10data.com]

  • Phosphorylase Kinase Deficiency

    […] of fructose metabolism E74.10 Disorder of fructose metabolism, unspecified E74.12 Hereditary fructose intolerance E74.19 Other disorders of fructose metabolism E74.2 Disorders[icd10data.com] E73.9 Lactose intolerance, unspecified E74 Other disorders of carbohydrate metabolism E74.0 Glycogen storage disease E74.09 Other glycogen storage disease E74.1 Disorders[icd10data.com] […] of fructose metabolism 2016 2017 2018 Non-Billable/Non-Specific Code Type 1 Excludes muscle phosphofructokinase deficiency ( E74.09 ) Andersen's disease E74.09 (glycogen[icd10data.com]

  • Toddler's Diarrhea

    Crohn’s disease (rare in children) Cystic fibrosis Primary lactose intolerance (rare in toddlers) Hereditary fructose intolerance (rare) Treatment Treatment of toddler’s diarrhea[healthhype.com]

  • DiGeorge Syndrome

    Diseases & Conditions Hereditary fructose intolerance Hereditary fructose intolerance is a disorder in which a person lacks the protein needed to break down fructose.[mountsinai.org]

  • Pontocerebellar Hypoplasia Type 1B

    fructose intolerance Herlitz junctional epidermolysis bullosa, LAMA3-related Herlitz junctional epidermolysis bullosa, LAMB3-related Herlitz junctional epidermolysis bullosa[jewishgenetics.org] HADHA-related Disorders (including Long Chain 3-Hydroxyacal-CoA Dehydrogenase Deficiency) Hb beta chain-related hemoglobinopathy (including beta thalassemia and sickle cell disease) Hereditary[jewishgenetics.org]

  • Hereditary Multiple Intestinal Atresia

    […] angioedema Hereditary breast cancer Hereditary chronic pancreatitis Hereditary fructose intolerance Hereditary hearing loss Hereditary hemorrhagic telangiectasia Hereditary[igenomix.us] GSS syndrome Harlequin type ichthyosis congenital Hemolytic anemia due to red cell pyruvate kinase deficiency Hemophagocytic lymphohistiocytosis Hemophilia A Hemophilia B Hereditary[igenomix.us]

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