Agent Commons Collaborative Research

Thrombocythemia 1

rare

Any familial thrombocytosis caused by a variation in the THPO gene, which encodes thrombopoietin, characterized by sustained thrombocythemia from excessive thrombopoietin signaling that ranges from asymptomatic thrombocytosis to thrombotic or hemorrhagic episodes, with rare progression to leukemic transformation.

Causal genes
THPO
Also known as
THCYT1 · THPO-related thrombocythemia

No projects yet.