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Results 21 - 30 of 87 for vitamin D
  1. Progressive familial intrahepatic cholestasis 
    ... pancreatitis), and low levels of fat-soluble vitamins (vitamins A, D, E, and K) in the blood. Affected individuals ...
    https://medlineplus.gov/...ressive-familial-intrahepatic-cholestasis - Genetics
  2. Donnai-Barrow syndrome 
    ... in various body processes, including the absorption of vitamins A and D, immune functioning, stress response, and the transport of ...
    https://medlineplus.gov/genetics/condition/donnai-barrow-syndrome - Genetics
  3. LRP2 gene 
    ... in various body processes, including the absorption of vitamins A and D, immune functioning, stress response, and the transport of ...
    https://medlineplus.gov/genetics/gene/lrp2 - Genetics
  4. SAR1B gene 
    ... Chylomicrons are needed to absorb fat-soluble vitamins (vitamins K, E, and D) and carry fats and cholesterol from the small ... absorption (malabsorption) of dietary fats and fat-soluble vitamins, leading to nutritional and developmental problems in people with ... Charcosset M, Sassolas A, Peretti N, Roy CC, Deslandres C, Sinnett D, Levy E, Lachaux A. Anderson or chylomicron retention ...
    https://medlineplus.gov/genetics/gene/sar1b - Genetics
  5. Ataxia with vitamin E deficiency 
    ... for Rare Disorders (NORD) ClinicalTrials.gov ATAXIA WITH VITAMIN E DEFICIENCY; AVED PubMed Bromley D, Anderson PC, Daggett V. Structural consequences of mutations ...
    https://medlineplus.gov/.../ataxia-with-vitamin-e-deficiency - Genetics
  6. Methylmalonic acidemia with homocystinuria 
    ... doi: 10.1056/NEJMoa072200. Citation on PubMed Froese DS, Fowler B, Baumgartner MR. Vitamin B12 , folate, and the methionine remethylation cycle-biochemistry, ...
    https://medlineplus.gov/...ethylmalonic-acidemia-with-homocystinuria - Genetics
  7. TTPA gene 
    ... D, Mani B, Stocker A, Atkinson J, Manor D. Molecular determinants of heritable vitamin E deficiency. Biochemistry. 2004 Apr 13;43(14): ... Suzuki J. Clinicopathological report of retinitis pigmentosa with vitamin E ... J, Manor D. Biochemical consequences of heritable mutations in the alpha- ...
    https://medlineplus.gov/genetics/gene/ttpa - Genetics
  8. CUBN gene 
    ... anemia 1 causes impaired recognition of intrinsic factor-vitamin B(12) by cubilin. Blood. 2000 Jul 15;96(2):405-9. Citation on PubMed Watkins D, Rosenblatt DS. Lessons in biology from patients with ...
    https://medlineplus.gov/genetics/gene/cubn - Genetics
  9. MMADHC gene 
    ... B. Gene identification for the cblD defect of vitamin B12 metabolism. N Engl J Med. 2008 Apr 3;358(14):1454-64. doi: 10.1056/NEJMoa072200. Citation on PubMed Froese DS, Kopec J, Fitzpatrick F, Schuller M, McCorvie TJ, ...
    https://medlineplus.gov/genetics/gene/mmadhc - Genetics
  10. FOLR1 gene 
    ... Free article on PubMed Central Watkins D, Rosenblatt DS. Update and new concepts in vitamin responsive disorders of folate transport and metabolism. J ...
    https://medlineplus.gov/genetics/gene/folr1 - Genetics
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