Platelet-type bleeding disorder 20

Any inherited bleeding disorder, platelet-type in which the cause of the disease is a mutation in the SLFN14 gene.

Also known as: BDPLT20, SLFN14 inherited bleeding disorder, platelet-type, autosomal dominant thrombocytopenia with platelet secretion defect, bleeding disorder, platelet-type, 20, inherited bleeding disorder, platelet-type caused by mutation in SLFN14

10 clinical trials for this condition and its sub-types, 0 tagged with Platelet-type bleeding disorder 20 itself.