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Summary Literature (0)
MIM:251000 - METHYLMALONIC ACIDURIA DUE TO METHYLMALONYL-CoA MUTASE DEFICIENCY; MAMM

Xenbase Genes: mmut

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009612 - methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency
MONDO:0017360 - vitamin B12-unresponsive methylmalonic acidemia type mut0
MONDO:0019267 - gray matter of midbrain

Disease Ontology (DO):
DOID:0060740 - methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency