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Results 1 - 10 of 41 for vitamin b
  1. Imerslund-Gräsbeck syndrome 
    ... IGS1 PubMed Grasbeck R. Imerslund-Grasbeck syndrome (selective vitamin B(12) malabsorption with proteinuria). Orphanet J Rare Dis. ... anemia 1 causes impaired recognition of intrinsic factor-vitamin B(12) by cubilin. Blood. 2000 Jul 15;96( ...
    https://medlineplus.gov/.../condition/imerslund-grasbeck-syndrome - Genetics
  2. Cerebral folate transport deficiency 
    ... that develops from a shortage (deficiency) of the B-vitamin folate (also called vitamin B9) in the brain. ...
    https://medlineplus.gov/.../cerebral-folate-transport-deficiency - Genetics
  3. Methylmalonic acidemia with homocystinuria 
    ... LMBRD1: the gene for the cblF defect of vitamin B(1)(2) metabolism. J Inherit Metab Dis. 2011 ...
    https://medlineplus.gov/...ethylmalonic-acidemia-with-homocystinuria - Genetics
  4. Hereditary folate malabsorption 
    ... digestion, the body cannot take in (absorb) certain B vitamins called folates. Folates are important for cell growth ...
    https://medlineplus.gov/.../hereditary-folate-malabsorption - Genetics
  5. Biotinidase deficiency 
    ... enzyme called biotinidase. This enzyme recycles biotin, a B vitamin found in foods such as liver, egg yolks, ... Epub 2010 Jan 11. Citation on PubMed Wolf B. The neurology of biotinidase deficiency. Mol ... Epub 2011 Jun 12. Citation on PubMed
    https://medlineplus.gov/genetics/condition/biotinidase-deficiency - Genetics
  6. Glutamate formiminotransferase deficiency 
    ... their urine, they have elevated amounts of certain B vitamins (called folates) in their blood.The severe form ...
    https://medlineplus.gov/...glutamate-formiminotransferase-deficiency - Genetics
  7. Holocarboxylase synthetase deficiency 
    ... important for the effective use of biotin, a B vitamin found in foods such as liver, egg yolks, ...
    https://medlineplus.gov/.../holocarboxylase-synthetase-deficiency - Genetics
  8. Vitamin D-dependent rickets 
    ... TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR; VDDR2B VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A; VDDR1A PubMed Chen H, Hewison M, Hu B, Adams JS. Heterogeneous nuclear ribonucleoprotein (hnRNP) binding to ...
    https://medlineplus.gov/.../condition/vitamin-d-dependent-rickets - Genetics
  9. Ataxia with vitamin E deficiency 
    ... D, Piacentini S, Squitieri F, Capra R, Castellotti B, Di Donato S. Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and ...
    https://medlineplus.gov/.../ataxia-with-vitamin-e-deficiency - Genetics
  10. Intervertebral disc disease 
    ... Citation on PubMed Toktas ZO, Eksi MS, Yilmaz B, Demir MK, Ozgen S, Kilic T, Konya D. Association of collagen I, IX and vitamin D receptor gene polymorphisms with radiological severity of ...
    https://medlineplus.gov/.../condition/intervertebral-disc-disease - Genetics
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