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Results 1 - 10 of 14 for Cobalamin deficiency
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  1. MMAB gene 
    ... cblB CFAP23 cob(I)alamin adenosyltransferase methylmalonic aciduria (cobalamin deficiency) cblB type methylmalonic aciduria (cobalamin deficiency) type B ...
    https://medlineplus.gov/genetics/gene/mmab - Genetics
  2. MMAA gene 
    ... More About This Health Condition cblA methylmalonic aciduria (cobalamin deficiency) cblA type methylmalonic aciduria (cobalamin deficiency) type A methylmalonic aciduria type A MMAA_HUMAN ...
    https://medlineplus.gov/genetics/gene/mmaa - Genetics
  3. MMACHC gene 
    ... About This Health Condition cblC DKFZP564I122 methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria methylmalonic aciduria and homocystinuria ...
    https://medlineplus.gov/genetics/gene/mmachc - Genetics
  4. MMADHC gene 
    ... This Health Condition C2orf25 cblD CL25022 methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria methylmalonic aciduria and homocystinuria ...
    https://medlineplus.gov/genetics/gene/mmadhc - Genetics
  5. Methylmalonic acidemia with homocystinuria 
    ... Huemer M, Baumgartner MR. The clinical presentation of cobalamin-related disorders: From acquired deficiencies to inborn errors of absorption and intracellular pathways. ...
    https://medlineplus.gov/...ethylmalonic-acidemia-with-homocystinuria - Genetics
  6. 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 ...
    https://medlineplus.gov/genetics/condition/transcobalamin-deficiency - Genetics
  7. TCN2 gene 
    ... TCN2 gene have been found to cause transcobalamin deficiency. This condition impairs the transport of cobalamin from the bloodstream to cells throughout the body. ...
    https://medlineplus.gov/genetics/gene/tcn2 - Genetics
  8. Glutamate formiminotransferase deficiency 
    ... PubMed Whitehead VM. Acquired and inherited disorders of cobalamin and folate in children. Br J Haematol. 2006 Jul;134(2):125-36. doi: 10.1111/j.1365-2141.2006.06133.x. Citation on PubMed
    https://medlineplus.gov/...glutamate-formiminotransferase-deficiency - Genetics
  9. MTRR gene 
    ... Gravel RA. Molecular basis for methionine synthase reductase deficiency in patients belonging to the cblE complementation group of disorders in folate/cobalamin metabolism. Hum Mol Genet. 1999 Oct;8(11): ...
    https://medlineplus.gov/genetics/gene/mtrr - Genetics
  10. HLCS gene 
    ... NCBI Gene ClinVar ... responsiveness in biotin-responsive multiple carboxylase deficiency. Mol Genet Metab. 1999 Feb;66(2):80- ...
    https://medlineplus.gov/genetics/gene/hlcs - Genetics
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