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Results 21 - 30 of 41 for vitamin D
  1. Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy 
    ... features of APECED, such as CMC, hypoparathyroidism, or vitamin B12 deficiency, but do not have the full pattern of ... or Free article on PubMed Central De Martino L, Capalbo D, Improda N, D'Elia F, Di Mase R, ...
    https://medlineplus.gov/...inopathy-candidiasis-ectodermal-dystrophy - Genetics
  2. Transcobalamin deficiency 
    ... Jul 6. Citation on PubMed Prasad C, Rosenblatt DS, Corley K, ... 2014 Feb 22. Citation on PubMed
    https://medlineplus.gov/genetics/condition/transcobalamin-deficiency - Genetics
  3. Thiamine-responsive megaloblastic anemia syndrome 
    ... without the help of a transporter when the vitamin is present in large amounts.It remains unclear exactly how ... Baron D, Assaraf YG, Cohen N, Aronheim A. Lack of ...
    https://medlineplus.gov/...-responsive-megaloblastic-anemia-syndrome - Genetics
  4. Nonketotic hyperglycinemia 
    ... molecule is added to and used by a vitamin called folate. Folate is required for many functions in the cell ... Aliefendioglu D, Tana Aslan Ay, Coskun T, Dursun A, Cakmak ...
    https://medlineplus.gov/.../condition/nonketotic-hyperglycinemia - Genetics
  5. Hartnup disease 
    ... be lacking (deficient) in certain amino acids and vitamins. However, individuals who are nutrient-deficient due to their ... Citation on PubMed Camargo SM, Singer D, Makrides V, Huggel K, Pos KM, Wagner CA, ...
    https://medlineplus.gov/genetics/condition/hartnup-disease - Genetics
  6. Factor VII deficiency 
    ... that prevent clotting, or by a deficiency of vitamin K. ... Mariani G, Herrmann FH, Dolce A, Batorova A, Etro D, Peyvandi F, Wulff K, Schved JF, Auerswald G, ...
    https://medlineplus.gov/genetics/condition/factor-vii-deficiency - Genetics
  7. Protein S deficiency 
    ... variants. Causes of acquired protein S deficiency include vitamin K deficiency, liver disease, and kidney ... Citation on PubMed Pintao MC, Garcia AA, Borgel D, Alhenc-Gelas M, Spek CA, de Visser MC, ...
    https://medlineplus.gov/genetics/condition/protein-s-deficiency - Genetics
  8. Biotin-thiamine-responsive basal ganglia disease 
    ... into cells, resulting in decreased absorption of the vitamin and leading to neurological dysfunction. ... Debs R, Depienne C, Rastetter A, Bellanger A, Degos B, Galanaud D, Keren B, Lyon-Caen O, Brice A, Sedel ...
    https://medlineplus.gov/...thiamine-responsive-basal-ganglia-disease - Genetics
  9. Familial hypobetalipoproteinemia 
    ... s ability to absorb fats and fat-soluble vitamins from the diet.Although APOB gene mutations are responsible for ... Fasano T, Cefalu AB, Di Leo E, Noto D, Pollaccia D, Bocchi L, Valenti V, Bonardi R, ...
    https://medlineplus.gov/.../familial-hypobetalipoproteinemia - Genetics
  10. Warfarin sensitivity 
    ... The VKORC1 gene provides instructions for making a vitamin K epoxide reductase enzyme. The VKORC1 enzyme ... PubMed Central Flockhart DA, O'Kane D, Williams MS, Watson MS, Flockhart DA, Gage B, ...
    https://medlineplus.gov/genetics/condition/warfarin-sensitivity - Genetics
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