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Results 1 - 10 of 10 for COPPER OR FOLIC ACID OR NIACIN OR PYRIDOXINE OR ZINC
  1. Spina bifida 
    ... have shown that women who take supplements containing folic acid (the synthetic form of folate) before they get ... a.32937. No abstract available. Citation on PubMed Folic acid for the prevention of neural tube defects. American ...
    https://medlineplus.gov/genetics/condition/spina-bifida - Genetics
  2. Hereditary folate malabsorption 
    ... Congenital defect of folate absorption Congenital folate malabsorption Folic acid transport defect Genetic Testing Registry: Congenital defect of ... K, Dlamini JC, Ivashkin V. The Concept of Folic Acid in Health and Disease. Molecules. 2021 Jun 18; ...
    https://medlineplus.gov/.../hereditary-folate-malabsorption - Genetics
  3. Homocystinuria 
    ... to have shortages (deficiencies) of vitamin B12 and folic acid. Cystathionine beta synthase deficiency Homocysteinemia Genetic Testing Registry: ... classical homocystinuria at risk of vitamin B12 and folic acid deficiency? Mol Genet Metab. 2007 Sep-Oct;92( ...
    https://medlineplus.gov/genetics/condition/homocystinuria - Genetics
  4. SOD1 gene 
    ... Central Valentine JS, Doucette PA, Zittin Potter S. Copper-zinc superoxide dismutase and amyotrophic lateral sclerosis. Annu Rev ...
    https://medlineplus.gov/genetics/gene/sod1 - Genetics
  5. Anencephaly 
    ... have shown that women who take supplements containing folic acid (the synthetic form of folate) before they get ...
    https://medlineplus.gov/genetics/condition/anencephaly - Genetics
  6. ATP7B gene 
    ... change one of the protein building blocks (amino acids) used to make copper-transporting ATPase 2. This type of mutation alters ... structure of the protein or its stability, preventing copper-transporting ... common amino acid substitution replaces the amino acid histidine with the ...
    https://medlineplus.gov/genetics/gene/atp7b - Genetics
  7. Wilson disease 
    ... tissues and appears to be involved in transporting copper. Studies have focused on the effects of a PRNP gene variation that affects position 129 of the prion protein. At this position, people can have either the protein building block (amino acid) methionine or the amino acid valine. Among people ...
    https://medlineplus.gov/genetics/condition/wilson-disease - Genetics
  8. Cutis laxa 
    ... Menkes syndrome, which is a condition that affects copper levels in the body. In addition to sagging ... making a protein that is important for regulating copper levels in the body. Variants in the ATP7A ...
    https://medlineplus.gov/genetics/condition/cutis-laxa - Genetics
  9. PRNP gene 
    ... Met or Val/Val) instead of different amino acids (Met/Val). People with Met/Met at ... in which excessive amounts of copper build up in the body. Wilson disease is ...
    https://medlineplus.gov/genetics/gene/prnp - Genetics
  10. CP gene 
    ... Citation on PubMed Nittis T, Gitlin JD. The copper-iron connection: hereditary aceruloplasminemia. Semin Hematol. 2002 Oct; ...
    https://medlineplus.gov/genetics/gene/cp - Genetics