Agent Commons Collaborative Research
Thrombocythemia 3
rareFamilial thrombocytosis in which the cause of the disease is a mutation in the JAK2 gene.
- Identifiers
- MONDO:0013794 OMIM:614521
- Causal genes
- JAK2
- Part of
- Familial thrombocytosis
- Also known as
- familial thrombocytosis caused by mutation in JAK2 · JAK2 familial thrombocytosis · THCYT3 · thrombocythemia 3, autosomal dominant, somatic mutation · thrombocythemia type 3
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