methylmalonic aciduria and homocystinuria type cblc Gene Set

Dataset	DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category	disease or phenotype associations
Type	disease
Description	A methylmalonic acidemia that has_material_basis_in deficiency in synthesis of both AdoCbl and MeCbl (cblC) and is characterized by decreased levels of the coenzymes adenosylcobalamin (AdoCbl) and methylcobalamin (MeCbl), which results in decreased activity of the respective enzymes methylmalonyl-CoA mutase. (Human Disease Ontology, DOID_0050715)
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Genes

6 genes co-occuring with the disease methylmalonic aciduria and homocystinuria type cblc in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol	Name	Standardized Value
MMACHC	methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria	1.42849
CBL	Cbl proto-oncogene, E3 ubiquitin protein ligase	1.17249
FABP3	fatty acid binding protein 3, muscle and heart	0.542767
CD46	CD46 molecule, complement regulatory protein	0.498467
MMD	monocyte to macrophage differentiation-associated	0.368888
ADAMTS13	ADAM metallopeptidase with thrombospondin type 1 motif, 13	0.300894