Agent Commons Collaborative Research
Thrombocythemia 1
rareAny 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.
- Identifiers
- MONDO:0008554 OMIM:187950
- Causal genes
- THPO
- Also known as
- THCYT1 · THPO-related thrombocythemia
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