decreased methionine synthase activity Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	A reduction in methionine synthase activity. (Human Phenotype Ontology, HP_0003524)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0003524
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Genes

5 genes associated with the decreased methionine synthase activity 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
MTRR	5-methyltetrahydrofolate-homocysteine methyltransferase reductase