Methylmalonic acidemia Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An organic acidemia that involves an accumulation of methylmalonic acid in the blood. (Human Disease Ontology, DOID_14749)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C537358
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Genes

10 genes/proteins associated with the disease Methylmalonic acidemia from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
SOD2 superoxide dismutase 2, mitochondrial 2.88009
SUCLG2 succinate-CoA ligase, GDP-forming, beta subunit 2.88009
CYCS cytochrome c, somatic 2.88009
SEPT11 septin 11 2.88009
SEPT2 septin 2 2.88009
GPD2 glycerol-3-phosphate dehydrogenase 2 (mitochondrial) 2.88009
MUT methylmalonyl CoA mutase 2.88009
CRABP2 cellular retinoic acid binding protein 2 2.88009
ACSF3 acyl-CoA synthetase family member 3 2.88009
PTRF polymerase I and transcript release factor 2.88009