Thrombocythemia 2

Familial thrombocytosis in which the cause of the disease is a mutation in the MPL gene.

Also known as: MPL familial thrombocytosis, familial thrombocytosis caused by mutation in MPL, thrombocythemia 2, thrombocythemia 2, autosomal dominant, somatic mutation, thrombocythemia type 2, THCYT2

35 clinical trials for this condition and its sub-types.