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

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