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ICD-10 Coding for Myeloproliferative Disease(D47.1, C94.4)

Complete ICD-10-CM coding and documentation guide for Myeloproliferative Disease. Includes clinical validation requirements, documentation requirements, and coding pitfalls.

Also known as:

Chronic Myeloproliferative DisorderMyelodysplastic/Myeloproliferative Neoplasm

Related ICD-10 Code Ranges

Complete code families applicable to Myeloproliferative Disease

D47-D47.9Primary Range

Other Neoplasms of Uncertain Behavior of Lymphoid, Hematopoietic and Related Tissue

This range includes codes for chronic myeloproliferative diseases, which are primary for this condition.

Myeloid Leukemia

Includes codes for specific myeloid leukemias that may be differentially diagnosed from myeloproliferative diseases.

Code Comparison: When to Use Each Code

Compare key differences between these codes to ensure accurate selection

CodeDescriptionWhen to UseKey Documentation
D47.1Chronic myeloproliferative diseaseUse when a specific subtype of myeloproliferative disease is not identified.
  • JAK2, CALR, or MPL mutation testing
  • Bone marrow biopsy results
C94.4Polycythemia veraUse when polycythemia vera is confirmed by clinical and laboratory findings.
  • Hemoglobin >16.5 g/dL (men) or >16.0 g/dL (women)
  • JAK2 V617F mutation positive

Clinical Decision Support

Always review the patient's clinical documentation thoroughly. When in doubt, choose the more specific code and ensure documentation supports it.

Key Information: ICD-10 code for myeloproliferative disease

Essential facts and insights about Myeloproliferative Disease

The ICD-10 code for chronic myeloproliferative disease is D47.1.

Primary ICD-10-CM Codes for myeloproliferative disease

Chronic myeloproliferative disease
Billable Code

Decision Criteria

clinical Criteria

  • JAK2, CALR, or MPL mutation positive

Applicable To

  • Chronic eosinophilic leukemia
  • Myelodysplastic/myeloproliferative neoplasm

Excludes

  • C92.1_ (Chronic myeloid leukemia, BCR/ABL-positive)
  • D75.81 (Myelofibrosis)

Clinical Validation Requirements

  • JAK2, CALR, or MPL mutation testing
  • Bone marrow biopsy results

Code-Specific Risks

  • Incorrectly using D47.1 for specific subtypes like polycythemia vera or essential thrombocythemia.

Coding Notes

  • Ensure genetic testing results are documented to support the use of this code.

Ancillary Codes

Additional codes that should be used in conjunction with the main diagnosis codes when applicable.

Splenomegaly

R16.1
Use when splenomegaly is present as a symptom.

Differential Codes

Alternative codes to consider when ruling out similar conditions to the primary diagnosis.

Chronic myeloid leukemia, BCR/ABL-positive

C92.1
Presence of BCR/ABL1 fusion gene.

Documentation & Coding Risks

Avoid these common documentation and coding issues when documenting Myeloproliferative Disease to ensure proper reimbursement, maintain compliance, and reduce audit risk. These guidelines are particularly important when using ICD-10 code D47.1.

Impact

Clinical: Inaccurate diagnosis and treatment planning., Regulatory: Non-compliance with coding standards., Financial: Potential claim denials.

Mitigation Strategy

Ensure all genetic test results are included in the patient's medical record.

Impact

Reimbursement: Incorrect reimbursement due to misclassification., Compliance: Non-compliance with coding guidelines., Data Quality: Inaccurate clinical data representation.

Mitigation Strategy

Use specific codes like C94.4 for polycythemia vera.

Impact

Lack of genetic test documentation can lead to audit risks.

Mitigation Strategy

Ensure all genetic test results are documented in the patient's record.

Documentation errors, coding pitfalls, and audit risks are interconnected aspects of medical coding and billing. Addressing all three areas helps ensure accurate coding, optimal reimbursement, and regulatory compliance.

Frequently Asked Questions

Common questions about ICD-10 coding for Myeloproliferative Disease, with expert answers to help guide accurate code selection and documentation.

Documentation Templates for Myeloproliferative Disease

Use these documentation templates to ensure complete and accurate documentation for Myeloproliferative Disease. These templates include all required elements for proper coding and billing.

Chronic myeloproliferative disease with genetic testing

Specialty: Hematology

Required Elements

  • Patient demographics
  • Clinical presentation
  • Genetic test results
  • Bone marrow biopsy findings

Example Documentation

Patient presents with splenomegaly and elevated blood counts. JAK2 V617F mutation positive. Bone marrow biopsy shows hypercellularity.

Examples: Poor vs. Good Documentation

Poor Documentation Example
Patient has elevated blood counts.
Good Documentation Example
Patient presents with elevated blood counts, JAK2 V617F mutation positive, hypercellular marrow with trilineage hyperplasia.
Explanation
The good example provides specific genetic and clinical findings supporting the diagnosis.

Need help with ICD-10 coding for Myeloproliferative Disease? Ask your questions below.

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