Acatalasia
MONDO:0013571A congenital disorder resulting from a deficiency in erythrocyte catalase, an enzyme responsible for the breakdown of hydrogen peroxide.
Also known as: acatalasemia, acatalasia, catalase deficiency
1 clinical trial for this condition and its sub-types, 0 tagged with Acatalasia itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.