S3866 Genetic analysis for a specific gene mutation for hypertrophic cardiomyopathy (hcm) in an individual with a known hcm mutation in the family
Short descriptor: Spec gene test hyp cardiomy
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S3866 is the HCPCS Level II code for Genetic analysis for a specific gene mutation for hypertrophic cardiomyopathy (hcm) in an individual with a known hcm mutation in the family (2026). It belongs to Section S — Temporary National Codes (Non-Medicare). Under Medicare, its coverage status is: Not payable by Medicare. Part B pricing methodology: Not separately priced by Part B.
Classification & CMS Attributes
- Medicare Coverage
- Not payable by Medicare (code I)
- Part B Pricing
- Not separately priced by Part B (indicator 00)
- Type of Service
- Other medical items or services
- Effective Date
- 2009-04-01
- 2026 Maintenance
- No change this year
References
Cite This Page
Reference S3866 with the canonical source and edition:
S3866 — Genetic analysis for a specific gene mutation for hypertrophic cardiomyopathy (hcm) in an individual with a known hcm mutation in the family. ICD-10 Coding Pro (HCPCS Level II 2026). https://icd10codingpro.com/hcpcs-codes/S3866
Canonical URL: https://icd10codingpro.com/hcpcs-codes/S3866