Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
MIM:251000 - METHYLMALONIC ACIDURIA DUE TO METHYLMALONYL-CoA MUTASE DEFICIENCY


Xenbase Genes: mmut

Human Disease Resource: OMIM

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 - vitamin B12-unresponsive methylmalonic acidemia type mut-

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