Genomic Sequencing Procedure for Severe Inherited Conditions (81443) (November 2018)

Why This Topic Matters

The article helps readers recognize when the CPT update affects carrier screening and related genetic testing workflows. It also places the new code in the context of other molecular pathology codes and related tests so users can compare the general subject matter covered by the guidance.

Article Sections

1. November 2018 page 9

   Introductory article header and publication context for the CPT update.

2. Genomic Sequencing Procedures and Other Molecular Multianalyte Assays

   Overview of the new genomic sequencing procedure code and its relationship to other molecular testing categories. The section also discusses the broader setting in which the code update appears.

3. Coding Tip

   General coding guidance on how certain molecular pathology analyte procedures are organized across Tier 1, Tier 2, and unlisted reporting categories.

4. Clinical Example (81443)

   A representative clinical scenario showing the type of patient context associated with the code update and the related testing workflow.

5. Description of Procedure (81443)

   A procedural overview of laboratory and reporting steps associated with the testing process described in the article.