S3844 Dna analysis of the connexin 26 gene (gjb2) for susceptibility to congenital, profound deafness
Short descriptor: Dna analysis deafness
Look up S3844 alongside ICD-10-CM diagnoses, the HCPCS Table of Drugs, and the AI coding assistant.
S3844 is the HCPCS Level II code for Dna analysis of the connexin 26 gene (gjb2) for susceptibility to congenital, profound deafness (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
- 2003-07-01
- 2026 Maintenance
- No change this year
References
Cite This Page
Reference S3844 with the canonical source and edition:
S3844 — Dna analysis of the connexin 26 gene (gjb2) for susceptibility to congenital, profound deafness. ICD-10 Coding Pro (HCPCS Level II 2026). https://icd10codingpro.com/hcpcs-codes/S3844
Canonical URL: https://icd10codingpro.com/hcpcs-codes/S3844