D47.3

Applicable To

• Essential thrombocytosis

• Idiopathic hemorrhagic thrombocythemia

• Primary thrombocytosis

Approximate Synonyms

• Essential thrombocythemia

• Thrombocytosis

• Thrombocytosis high blood platelets)

Clinical Information

• A chronic myeloproliferative neoplasm that involves primarily the megakaryocytic lineage. It is characterized by sustained thrombocytosis in the blood, increased numbers of large, mature megakaryocytes in the bone marrow, and episodes of thrombosis and/or hemorrhage. The cause is unknown. Median survival times of 10-15 years are commonly reported. who, 2008)

• A clinical syndrome characterized by repeated spontaneous hemorrhages and a remarkable increase in the number of circulating platelets.

• An increased number of thrombocytes platelets) in the blood, without a known cause.

• Clinical syndrome characterized by repeated spontaneous hemorrhages and a remarkable increase in the number of circulating platelets.

Details

• D47.3 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.

• The 2023 edition of ICD-10-CM D47.3 became effective on October 1, 2022.

• This is the American ICD-10-CM version of D47.3 – other international versions of ICD-10 D47.3 may differ.