81319 Pms2 gene dup/delet variants
Also known as: PMS2 copy number analysis, PMS2 deletion duplication testing
Post-Meiotic Segregation Increased 2 (PMS2) gene duplication and deletion variant analysis for copy number variations in Lynch syndrome.
In Plain Language
PMS2 gene copy number test; Lynch syndrome copy variation detection
Clinical Context
Detects PMS2 deletions and duplications to improve diagnostic yield in Lynch syndrome diagnosis.
RVU Information
CPT 81319 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 81319?
CPT 81319 (Pms2 gene dup/delet variants) is a Pathology & Lab code. Post-Meiotic Segregation Increased 2 (PMS2) gene duplication and deletion variant analysis for copy number variations in Lynch syndrome.
Who uses CPT code 81319?
CPT 81319 is used by Pathology, Oncology, Gastroenterology. Detects PMS2 deletions and duplications to improve diagnostic yield in Lynch syndrome diagnosis.
When is CPT 81319 used?
Detects PMS2 deletions and duplications to improve diagnostic yield in Lynch syndrome diagnosis.
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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.