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Results 1 - 10 of 66 for vitamin k 2
  1. VKORC1 gene 
    ... or death. More About This Health Condition FLJ00289 vitamin K 1 2,3-epoxide reductase subunit 1 vitamin K epoxide reductase complex, subunit 1 VKOR Tests of ...
    https://medlineplus.gov/genetics/gene/vkorc1 - Genetics
  2. 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
  3. SLC34A1 gene 
    ... NEPHROLITHIASIS/OSTEOPOROSIS, HYPOPHOSPHATEMIC, 1; NPHLOP1 FANCONI RENOTUBULAR SYNDROME 2; FRTS2 NCBI Gene ClinVar Kido S, Kaneko I, Tatsumi S, Segawa H, Miyamoto K. Vitamin D and type II sodium-dependent phosphate cotransporters. ...
    https://medlineplus.gov/genetics/gene/slc34a1 - Genetics
  4. CYP27A1 gene 
    ... hydroxylase, cerebrotendinous xanthomatosis), polypeptide 1 sterol 27-hydroxylase vitamin D(3) 25-hydroxylase ... Wikvall K. Hormonal regulation of the human sterol 27-hydroxylase gene CYP27A1. Biochem J. 2003 Jun 1;372(Pt 2):529-34. doi: 10.1042/BJ20021651. Citation on ...
    https://medlineplus.gov/genetics/gene/cyp27a1 - Genetics
  5. CYP24A1 gene 
    ... ClinVar Dinour D, Beckerman P, Ganon L, Tordjman K, Eisenstein Z, Holtzman EJ. Loss-of-function mutations of CYP24A1, the vitamin D 24-hydroxylase gene, cause long-standing hypercalciuric nephrolithiasis and nephrocalcinosis. J Urol. 2013 Aug;190(2):552-7. doi: 10.1016/j.juro.2013. ...
    https://medlineplus.gov/genetics/gene/cyp24a1 - Genetics
  6. MMACHC gene 
    ... EA, Coulton JW, Lepage P, Rommens JM, Morgan K, Rosenblatt DS. Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type. Nat Genet. 2006 Jan;38(1):93-100. doi: 10.1038/ng1683. Epub 2005 Nov 27. Citation on PubMed
    https://medlineplus.gov/genetics/gene/mmachc - Genetics
  7. OAT gene 
    ... and retina. J Clin Invest. 1988 Feb;81(2):630-3. doi: 10.1172/JCI113365. Citation on PubMed or Free article on PubMed Central Ohkubo Y, Ueta A, Ito T, Sumi S, Yamada M, Ozawa K, Togari H. Vitamin B6-responsive ornithine aminotransferase deficiency with a novel ...
    https://medlineplus.gov/genetics/gene/oat - Genetics
  8. PROS1 gene 
    ... PS21 PS22 PS23 PS24 PS25 PSA THPH5 THPH6 vitamin K-dependent plasma protein S Tests of PROS1 PubMed ...
    https://medlineplus.gov/genetics/gene/pros1 - Genetics
  9. 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
  10. ARSL gene 
    ... believe it participates in a chemical pathway involving vitamin K. Evidence suggests that vitamin K normally plays a role in bone growth and ...
    https://medlineplus.gov/genetics/gene/arsl - Genetics
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