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Results 1 - 10 of 16 for PYRIDOXINE OR COPPER OR NIACINAMIDE OR FOLIC ACID OR ZINC OR AZELAIC ACID
  1. Hereditary folate malabsorption 
    ... Congenital defect of folate absorption Congenital folate malabsorption Folic acid transport defect Genetic Testing Registry: Congenital defect of ...
    https://medlineplus.gov/.../hereditary-folate-malabsorption - Genetics
  2. 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
  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. 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
  5. 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
  6. ALDH7A1 gene 
    ... a form of vitamin B6 derived from food. Pyridoxine plays a role many processes in the body, such as the breakdown of amino acids and chemicals in the brain called neurotransmitters. It ...
    https://medlineplus.gov/genetics/gene/aldh7a1 - Genetics
  7. Pyridoxine-dependent epilepsy 
    ... vitamin B6 function builds up in various tissues. Pyridoxine plays a role in many processes in the body, such as the breakdown of amino acids and the productions of chemicals that transmit signals ...
    https://medlineplus.gov/.../condition/pyridoxine-dependent-epilepsy - Genetics
  8. 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
  9. Gyrate atrophy of the choroid and retina 
    ... the proper balance of protein building blocks (amino acids) in the body. This balance is important because a specific sequence of amino acids is required to build each of the many ...
    https://medlineplus.gov/.../gyrate-atrophy-of-the-choroid-and-retina - Genetics
  10. PRNP gene 
    ... Met or Val/Val) instead of different amino acids (Met/Val). Having Met/Met at ... excessive amounts of copper accumulate in the body. Wilson disease is caused ...
    https://medlineplus.gov/genetics/gene/prnp - Genetics
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