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ICD-10 Coding for BRCA Mutation(Z15.01, Z15.02)

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

Also known as:

BRCA1 MutationBRCA2 MutationBreast Cancer Susceptibility Genebrca12 genetic mutationhereditary breast ovarian cancer syndrome

Related ICD-10 Code Ranges

Complete code families applicable to BRCA Mutation

Z15.01-Z15.02Primary Range

Genetic susceptibility to malignant neoplasm of breast and ovary

These codes are used to identify patients with a confirmed BRCA1 or BRCA2 mutation, indicating a genetic susceptibility to breast and ovarian cancer.

Family history of primary malignant neoplasm

These codes are used to document family history of cancer, which may influence genetic testing and surveillance strategies.

Code Comparison: When to Use Each Code

Compare key differences between these codes to ensure accurate selection

CodeDescriptionWhen to UseKey Documentation
Z15.01Genetic susceptibility to malignant neoplasm of breastUse when a patient has a confirmed BRCA1 or BRCA2 mutation indicating increased risk for breast cancer.
  • Genetic test report confirming BRCA1/2 mutation
  • Provider documentation confirming genetic susceptibility
Z15.02Genetic susceptibility to malignant neoplasm of ovaryUse when a patient has a confirmed BRCA1 or BRCA2 mutation indicating increased risk for ovarian cancer.
  • Genetic test report confirming BRCA1/2 mutation
  • Provider documentation confirming genetic susceptibility

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 BRCA mutation

Essential facts and insights about BRCA Mutation

The ICD-10 code for BRCA mutation is Z15.01 for breast cancer susceptibility and Z15.02 for ovarian cancer susceptibility.

Primary ICD-10-CM Codes for brca

Genetic susceptibility to malignant neoplasm of breast
Billable Code

Decision Criteria

clinical Criteria

  • Confirmed BRCA1/2 mutation via genetic testing

documentation Criteria

  • Provider must document genetic susceptibility

Applicable To

  • BRCA1 mutation
  • BRCA2 mutation

Excludes

  • Family history of breast cancer (Z80.3)

Clinical Validation Requirements

  • Genetic test report confirming BRCA1/2 mutation
  • Provider documentation confirming genetic susceptibility

Code-Specific Risks

  • Incorrectly coding family history as personal genetic susceptibility.

Coding Notes

  • Ensure genetic test results are documented and linked to the code.

Ancillary Codes

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

Encounter for screening for other disorder

Z13.89
Use for screening encounters when no symptoms are present.

Differential Codes

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

Family history of malignant neoplasm of breast

Z80.3
Use Z80.3 for documenting family history without confirmed personal genetic mutation.

Family history of malignant neoplasm of ovary

Z80.41
Use Z80.41 for documenting family history without confirmed personal genetic mutation.

Documentation & Coding Risks

Avoid these common documentation and coding issues when documenting BRCA Mutation to ensure proper reimbursement, maintain compliance, and reduce audit risk. These guidelines are particularly important when using ICD-10 code Z15.01.

Impact

Clinical: May lead to inappropriate surveillance or treatment., Regulatory: Non-compliance with coding guidelines., Financial: Potential claim denials due to incorrect coding.

Mitigation Strategy

Verify genetic test results before coding., Ensure provider documentation specifies personal vs. family history.

Impact

Reimbursement: Incorrect coding can lead to denied claims., Compliance: Using outdated codes can result in non-compliance with coding standards., Data Quality: Impacts the accuracy of patient records and data analytics.

Mitigation Strategy

Always use the most current ICD-10 codes, such as Z15.01 for BRCA1 mutation.

Impact

Using family history codes instead of genetic susceptibility codes.

Mitigation Strategy

Ensure genetic test results are reviewed and documented by the provider.

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 BRCA Mutation, with expert answers to help guide accurate code selection and documentation.

Documentation Templates for BRCA Mutation

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

Prophylactic Surgery in BRCA+ Patient

Specialty: Oncology

Required Elements

  • Genetic test confirmation
  • Provider documentation of mutation
  • Surgical plan and rationale

Example Documentation

Patient with BRCA2 mutation confirmed by genetic testing elects for prophylactic mastectomy due to increased cancer risk.

Examples: Poor vs. Good Documentation

Poor Documentation Example
Patient has BRCA mutation.
Good Documentation Example
BRCA2 mutation (c.5946delT) confirmed by genetic testing. Patient elects prophylactic mastectomy due to 45% lifetime breast cancer risk.
Explanation
The good example provides specific genetic details and clinical decision rationale.

Need help with ICD-10 coding for BRCA Mutation? Ask your questions below.

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