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Results 1 - 10 of 57 for Vitamin deficiency disorder
  1. Ataxia with vitamin E deficiency 
    Ataxia with vitamin E deficiency is a disorder that impairs the body's ability to use vitamin E obtained from the diet. Vitamin E is an ... Familial isolated deficiency of vitamin E Ataxia with vitamin E deficiency ... ClinicalTrials.gov ATAXIA WITH VITAMIN E DEFICIENCY; ...
    https://medlineplus.gov/.../ataxia-with-vitamin-e-deficiency - Genetics
  2. 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 ...
    https://medlineplus.gov/genetics/gene/cyp27b1 - Genetics
  3. Holocarboxylase synthetase deficiency 
    ... which the body is unable to use the vitamin biotin effectively. This disorder is classified as a multiple carboxylase deficiency, which is a group of disorders characterized by ...
    https://medlineplus.gov/.../holocarboxylase-synthetase-deficiency - Genetics
  4. Protein S deficiency 
    ... variants. Causes of acquired protein S deficiency include vitamin K deficiency, liver disease, and kidney disorders. PROS1 Protein S deficiency is typically inherited in ...
    https://medlineplus.gov/genetics/condition/protein-s-deficiency - Genetics
  5. Transcobalamin deficiency 
    Transcobalamin deficiency is a disorder that impairs the transport of cobalamin (also known as vitamin B12) within the body. Cobalamin is obtained from the diet; this vitamin is found in animal products ...
    https://medlineplus.gov/genetics/condition/transcobalamin-deficiency - Genetics
  6. Cerebral folate transport deficiency 
    Cerebral folate transport deficiency is a disorder that develops from a shortage (deficiency) of the B-vitamin folate (also called vitamin B9) in the brain. Affected children have normal development during infancy, but around age 2 they begin to ...
    https://medlineplus.gov/.../cerebral-folate-transport-deficiency - Genetics
  7. Biotinidase deficiency 
    Biotinidase deficiency is an inherited disorder in which the body is unable to recycle the vitamin biotin. If this condition is not recognized and treated, its signs and symptoms typically appear within the ...
    https://medlineplus.gov/genetics/condition/biotinidase-deficiency - Genetics
  8. Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy 
    ... features of APECED, such as CMC, hypoparathyroidism, or vitamin B12 deficiency, but do not have the full pattern of signs and symptoms that typically characterize the disorder. These individuals usually have one similarly-affected parent. ...
    https://medlineplus.gov/...inopathy-candidiasis-ectodermal-dystrophy - Genetics
  9. TTPA gene 
    ... is associated with the development of an eye disorder called retinitis pigmentosa that causes vision loss in people with ataxia with vitamin E deficiency.Mutations in the TTPA gene that cause no ...
    https://medlineplus.gov/genetics/gene/ttpa - Genetics
  10. Vitamin D-dependent rickets 
    ... and Cause an Atypical Form of Vitamin D Deficiency. J Clin Endocrinol Metab. 2015 Jul;100(7):E1005-13. doi: 10.1210/jc.2015-1746. Epub 2015 May 5. Citation on PubMed or Free article on PubMed Central
    https://medlineplus.gov/.../condition/vitamin-d-dependent-rickets - Genetics
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