Dyskeratosis congenita, autosomal recessive 2
MONDO:0013519A dyskeratosis congenita that has material basis in an autosomal recessive mutation of NOLA2 on chromosome 5q35.3.
Also known as: DKCB2, dyskeratosis congenita, autosomal recessive 2, dyskeratosis congenita, autosomal recessive type 2, autosomal recessive dyskeratosis congenita 2
32 clinical trials for this condition and its sub-types, 0 tagged with Dyskeratosis congenita, autosomal recessive 2 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.