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D47.3

Billable

Essential (hemorrhagic) thrombocythemia

HCC Category Mapping

V28HCC 23Melanoma and Other Skin Cancers
0.251
V24HCC 48Coagulation Defects and Other Specified Hematological Disorders
0.209
ESRDHCC 48Coagulation Defects and Other Specified Hematological Disorders
0.000
RxHCCHCC 21Hodgkin Lymphoma and Other Cancers
0.000

What This Code Means

Essential thrombocythemia is a blood disorder where the bone marrow produces too many platelets, which can lead to abnormal bleeding or clotting. This is a chronic condition that requires ongoing monitoring and management.

Coding Tips

  • Verify documentation specifies 'essential' or 'primary' thrombocythemia to distinguish from secondary causes of high platelet counts
  • Look for associated complications (thrombosis, hemorrhage) that may require additional codes, and confirm whether the patient is on antiplatelet or anticoagulant therapy

Clinical Significance

Essential thrombocythemia is a chronic myeloproliferative neoplasm characterized by persistent thrombocytosis (platelet count above 450,000/microL) due to clonal megakaryocyte proliferation. Despite being considered the most indolent of the myeloproliferative neoplasms, it carries risks of both thrombotic events (stroke, deep vein thrombosis) and paradoxical hemorrhagic complications from acquired von Willebrand disease.

Documentation Requirements

  • Documentation should include persistently elevated platelet counts, bone marrow biopsy showing megakaryocyte hyperplasia, and molecular testing (JAK2, CALR, or MPL mutations).
  • World Health Organization diagnostic criteria should be met.
  • Document cardiovascular risk factors, prior thrombotic events, and current therapy (aspirin, hydroxyurea, anagrelide).
  • Rule out reactive thrombocytosis.

Excludes 2 — Not included here, may code separately

Commonly Confused Codes

Code Hierarchy

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