81442 Noonan spectrum disorders
Also known as: Noonan syndrome genetics, RASopathy panel
Genetic testing panel for Noonan syndrome spectrum disorders.
In Plain Language
genetic test for Noonan syndrome; developmental delay gene testing
Clinical Context
Identifies mutations in RAS/MAPK pathway genes causing Noonan syndrome and related developmental disorders; affects growth and cardiac function.
RVU Information
CPT 81442 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 81442?
CPT 81442 (Noonan spectrum disorders) is a Pathology & Lab code. Genetic testing panel for Noonan syndrome spectrum disorders.
Who uses CPT code 81442?
CPT 81442 is used by genetics, pediatrics, molecular pathology. Identifies mutations in RAS/MAPK pathway genes causing Noonan syndrome and related developmental disorders; affects growth and cardiac function.
When is CPT 81442 used?
Identifies mutations in RAS/MAPK pathway genes causing Noonan syndrome and related developmental disorders; affects growth and cardiac function.
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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.