Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 33 for vitamin k 2
  1. Congenital bile acid synthesis defect type 2 
    ... absorb fats and fat-soluble vitamins, such as vitamins A, D, E, and K. People with congenital bile acid synthesis defect type 2 cannot produce (synthesize) bile acids, which are a ...
    https://medlineplus.gov/...genital-bile-acid-synthesis-defect-type-2 - Genetics
  2. X-linked chondrodysplasia punctata 1 
    ... thought to participate in a chemical pathway involving vitamin K. Evidence suggests that vitamin K normally plays a role in bone growth and ... linked recessive form. Hum Genet. 1989 May;82(2):167-70. doi: ... M, Rosenbaum K, Braverman N. Clinical and molecular analysis of arylsulfatase ...
    https://medlineplus.gov/.../x-linked-chondrodysplasia-punctata-1 - Genetics
  3. Warfarin resistance 
    ... The VKORC1 gene provides instructions for making a vitamin K epoxide reductase enzyme. The VKORC1 enzyme helps turn ... V, Conzelmann E, Hortnagel K, Pelz HJ, Lappegard K, Seifried E, Scharrer I, Tuddenham ... factor deficiency type 2. Nature. 2004 Feb 5;427(6974):537-41. ...
    https://medlineplus.gov/genetics/condition/warfarin-resistance - Genetics
  4. Warfarin sensitivity 
    ... The VKORC1 gene provides instructions for making a vitamin K epoxide reductase enzyme. The VKORC1 enzyme helps turn ... Lyon E, Nussbaum R, O'Kane D, Schulman K, Veenstra D, Williams MS, Watson ... Med. 2008 Feb;10(2):139-50. doi: 10.1097/GIM.0b013e318163c35f. Citation ...
    https://medlineplus.gov/genetics/condition/warfarin-sensitivity - Genetics
  5. Factor X deficiency 
    ... that prevent clotting, or by a deficiency of vitamin K. F10 When this condition is caused by mutations ...
    https://medlineplus.gov/genetics/condition/factor-x-deficiency - Genetics
  6. Methylmalonic acidemia with homocystinuria 
    ... LMBRD1: the gene for the cblF defect of vitamin B(1)(2) metabolism. J Inherit Metab Dis. 2011 Feb;34( ...
    https://medlineplus.gov/...ethylmalonic-acidemia-with-homocystinuria - Genetics
  7. Abetalipoproteinemia 
    ... a severe shortage (deficiency) of fat-soluble vitamins (vitamins A, E, and K). The signs and symptoms of this condition primarily ... R, Khan R, Pollex RL, Hegele RA. Abetalipoproteinemia: two case reports and literature ... PubMed or Free article on PubMed Central
    https://medlineplus.gov/genetics/condition/abetalipoproteinemia - Genetics
  8. Progressive familial intrahepatic cholestasis 
    ... pancreatitis), and low levels of fat-soluble vitamins (vitamins A, D, E, and K) in the blood. Affected individuals typically develop liver ...
    https://medlineplus.gov/...ressive-familial-intrahepatic-cholestasis - Genetics
  9. Permanent neonatal diabetes mellitus 
    ... in the genes encoding the pancreatic beta-cell K(ATP) channel subunits Kir6.2 (KCNJ11) and sulfonylurea receptor 1 (ABCC8) in diabetes ...
    https://medlineplus.gov/.../permanent-neonatal-diabetes-mellitus - Genetics
  10. Homocystinuria 
    ... Are heterocygotes for classical homocystinuria at risk of vitamin B12 and folic acid deficiency? Mol Genet Metab. 2007 Sep-Oct;92(1-2):100-3. doi: 10.1016/j.ymgme.2007. ...
    https://medlineplus.gov/genetics/condition/homocystinuria - Genetics
previous · 1 · 2 · 3 · 4 · next