81242 Fancc gene
Also known as: FANCC gene testing, Fanconi Anemia group C screening
Molecular analysis of the FANCC gene to identify mutations associated with Fanconi Anemia complementation group C.
In Plain Language
bone marrow failure gene test; genetic anemia screening
Clinical Context
Used to diagnose Fanconi Anemia group C in children with bone marrow failure, developmental abnormalities, and cancer predisposition.
RVU Information
CPT 81242 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 81242?
CPT 81242 (Fancc gene) is a Pathology & Lab code. Molecular analysis of the FANCC gene to identify mutations associated with Fanconi Anemia complementation group C.
Who uses CPT code 81242?
CPT 81242 is used by Genetics, Hematology, Pathology. Used to diagnose Fanconi Anemia group C in children with bone marrow failure, developmental abnormalities, and cancer predisposition.
When is CPT 81242 used?
Used to diagnose Fanconi Anemia group C in children with bone marrow failure, developmental abnormalities, and cancer predisposition.
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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.