Thrombocythemia 3

Familial thrombocytosis in which the cause of the disease is a mutation in the JAK2 gene.

Also known as: JAK2 familial thrombocytosis, familial thrombocytosis caused by mutation in JAK2, thrombocythemia 3, thrombocythemia 3, autosomal dominant, somatic mutation, thrombocythemia type 3, THCYT3, thrombocytosis 3

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