methylmalonic aciduria due to methylmalonyl-coa mutase deficiency

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency
MMUT Causal
1980486 27167370 9285782 15643616 28101778 19588269 10923046 7909321 15781192 7912889 9554742 1346616 1351030 17957493 9452100 17113806 26615597 8990001 25125334 1977311 11350191 1670635 22727635 16281286
ClinGen
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with methylmalonic aciduria due to methylmalonyl-coa mutase deficiency.
5 View disease cluster →
Methylmalonyl-coa mutase deficiency 1 shared geneMMUT Related via 1 shared gene including MMUT. Partial deficiency of methylmalonyl-coenzyme a mutase 1 shared geneMMUT Related via 1 shared gene including MMUT. Vitamin b12 deficiency 1 shared geneMMUT Related via 1 shared gene including MMUT. Vitamin b deficiency 1 shared geneMMUT Related via 1 shared gene including MMUT. Deficiency anemia 1 shared geneMMUT Related via 1 shared gene including MMUT.