MAN2B2 deficiency

MONDO:0800141

Any non-severe combined immunodeficiency in which the cause of the disease is variation in the MAN2B2 gene.

1 clinical trial for this condition and its sub-types, 0 tagged with MAN2B2 deficiency itself.

Where it sits in the disease tree

Part of

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.