abnormality of homocysteine metabolism Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	An abnormality of a homocysteine metabolic process. (Human Phenotype Ontology, HP_0010919)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0010919
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Genes

9 genes associated with the abnormality of homocysteine metabolism 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
CBS	cystathionine-beta-synthase
HCFC1	host cell factor C1
LMBRD1	LMBR1 domain containing 1
MMACHC	methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria
MMADHC	methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria
MTHFR	methylenetetrahydrofolate reductase (NAD(P)H)
MTR	5-methyltetrahydrofolate-homocysteine methyltransferase
MTRR	5-methyltetrahydrofolate-homocysteine methyltransferase reductase