81223 Cftr gene full sequence
Also known as: CFTR sequencing, CFTR full analysis
Complete sequence analysis of the CFTR gene to identify all point mutations and small indels associated with Cystic Fibrosis.
In Plain Language
cystic fibrosis gene test; comprehensive genetic testing
Clinical Context
Used for comprehensive Cystic Fibrosis screening in symptomatic individuals and carrier detection in at-risk populations.
RVU Information
CPT 81223 does not have a physician work RVU assigned by CMS. Reimbursement for this code is determined by payer-specific fee schedules.
Billing & Documentation
Lab and pathology codes require an order from the treating provider with clinical indication. For molecular pathology and genetic testing, document the specific analytes tested and clinical rationale.
How This Code Compares
This code has a work RVU of 0.00, meaning it does not have a physician work component assigned by CMS. In the Pathology & Lab category, 94% of codes share this characteristic.
Specialties
Frequently Asked Questions
What is CPT code 81223?
CPT 81223 (Cftr gene full sequence) is a Pathology & Lab code. Complete sequence analysis of the CFTR gene to identify all point mutations and small indels associated with Cystic Fibrosis.
Who uses CPT code 81223?
CPT 81223 is used by Genetics, Pulmonology, Pathology. Used for comprehensive Cystic Fibrosis screening in symptomatic individuals and carrier detection in at-risk populations.
When is CPT 81223 used?
Used for comprehensive Cystic Fibrosis screening in symptomatic individuals and carrier detection in at-risk populations.
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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.