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Results 1 - 10 of 14 for Low levels of vitamin K
  1. Progressive familial intrahepatic cholestasis 
    ... deafness, diarrhea, inflammation of the pancreas (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
  2. MTTP gene 
    ... soluble vitamins, such as vitamins E, A, and K. In the liver, ... Sufficient levels of fats, cholesterol, and vitamins are necessary for ...
    https://medlineplus.gov/genetics/gene/mttp - Genetics
  3. PURA syndrome 
    ... such as early sexual development (precocious puberty) or low levels of vitamin D (which is a hormone). PURA syndrome is ...
    https://medlineplus.gov/genetics/condition/pura-syndrome - Genetics
  4. Multiple sclerosis 
    ... such as exposure to the Epstein-Barr virus, low levels of vitamin D, and smoking.The HLA-DRB1 gene belongs ...
    https://medlineplus.gov/genetics/condition/multiple-sclerosis - Genetics
  5. FGFR1 gene 
    ... 60 percent of PMTs.PMTs often lead to low levels of vitamin D and phosphate in the blood (hypophosphatemia), resulting ...
    https://medlineplus.gov/genetics/gene/fgfr1 - Genetics
  6. SLC34A1 gene 
    ... the bloodstream. In an effort to raise the low phosphate levels caused by the loss of functional NaPi-IIa channels, vitamin D is activated. Too much active vitamin D ...
    https://medlineplus.gov/genetics/gene/slc34a1 - Genetics
  7. CYP27B1 gene 
    ... dependent rickets type 1A (VDDR1A), also known as vitamin D 1α-hydroxylase deficiency. This disorder of bone development is characterized by low levels of calcium (hypocalcemia) and phosphate (hypophosphatemia) in the ...
    https://medlineplus.gov/genetics/gene/cyp27b1 - Genetics
  8. LRP2 gene 
    ... A, Nakajima T, Fujita Y, Iino Y, Kamimura K, Bujo H, Saito Y, Emi M, Katayama Y. Genetic association of low-density lipoprotein receptor-related protein 2 (LRP2) with plasma lipid levels. J Atheroscler Thromb. 2007 Dec;14(6):310- ...
    https://medlineplus.gov/genetics/gene/lrp2 - Genetics
  9. F9 gene 
    ... R, Oldenburg J, Asmis L. Congenital hypersensitivity to vitamin K antagonists due to FIX propeptide mutation at locus - ...
    https://medlineplus.gov/genetics/gene/f9 - Genetics
  10. Familial hypobetalipoproteinemia 
    ... and transport fats. This condition is characterized by low levels of a fat-like substance called cholesterol in ...
    https://medlineplus.gov/.../familial-hypobetalipoproteinemia - Genetics
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