decreased methylmalonyl-coa mutase activity Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	An abnormality of Krebs cycle metabolism that is characterized by a decreased rate of methylmalonyl-CoA mutase activity. (Human Phenotype Ontology, HP_0003210)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0003210
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Genes

4 genes associated with the decreased methylmalonyl-coa mutase activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol	Name
MMAA	methylmalonic aciduria (cobalamin deficiency) cblA type
MMAB	methylmalonic aciduria (cobalamin deficiency) cblB type
MMACHC	methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria
MMADHC	methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria