decreased methylcobalamin Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Decreased concentration of methylcobalamin. Methylcobalamin is a form of vitamin B12. (Human Phenotype Ontology, HP_0003223)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003223
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Genes

6 genes associated with the decreased methylcobalamin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCD4 ATP-binding cassette, sub-family D (ALD), member 4
LMBRD1 LMBR1 domain containing 1
MMACHC methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria
MMADHC methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria
MTR 5-methyltetrahydrofolate-homocysteine methyltransferase
MTRR 5-methyltetrahydrofolate-homocysteine methyltransferase reductase