S3865 Complicated genet test hyp cardiomy
Also known as: hypertrophic cardiomyopathy panel, HCM genetic testing
Comprehensive genetic testing for multiple genes associated with hypertrophic cardiomyopathy including MYBPC3, MYH7, TNNT2, and other disease-associated loci.
In Plain Language
genetic test for thick heart muscle disease; cardiomyopathy gene panel
Clinical Context
Used in cardiology for diagnosis of hypertrophic cardiomyopathy and genetic counseling in affected patients and families.
RVU Information
CPT S3865 does not have a physician work RVU assigned by CMS. This is typical for supply, drug, and equipment codes — reimbursement is based on Average Sales Price (ASP), fee schedules, or payer contracts rather than the RVU system.
Billing & Documentation
S-codes are used by private payers (not Medicare) for services without a standard CPT or HCPCS code. Coverage varies significantly between insurers. Verify payer acceptance before billing and document medical necessity thoroughly.
Specialties
Frequently Asked Questions
What is CPT code S3865?
CPT S3865 (Complicated genet test hyp cardiomy) is a S Codes code. Comprehensive genetic testing for multiple genes associated with hypertrophic cardiomyopathy including MYBPC3, MYH7, TNNT2, and other disease-associated loci.
Is S3865 covered by insurance?
S3865 is a temporary HCPCS code. Coverage varies by payer and may change when permanent codes are assigned. Used in cardiology for diagnosis of hypertrophic cardiomyopathy and genetic counseling in affected patients and families.
When is CPT S3865 used?
Used in cardiology for diagnosis of hypertrophic cardiomyopathy and genetic counseling in affected patients and families.
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CPT® is a registered trademark of the American Medical Association. Data sourced from CMS Physician Fee Schedule RVU26A. Descriptions, synonyms, and clinical context are original content by RVU Edge.