81244 Fmr1 gen alys charac alleles
Also known as: FMR1 allele characterization, FMR1 repeat classification
Allele characterization of the FMR1 gene to measure and classify CGG repeat expansions in Fragile X Syndrome.
In Plain Language
fragile X test; repeat expansion measurement
Clinical Context
Used to classify FMR1 CGG repeats as normal, intermediate, premutation, or full mutation for disease severity assessment.
RVU Information
CPT 81244 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 81244?
CPT 81244 (Fmr1 gen alys charac alleles) is a Pathology & Lab code. Allele characterization of the FMR1 gene to measure and classify CGG repeat expansions in Fragile X Syndrome.
Who uses CPT code 81244?
CPT 81244 is used by Genetics, Neurology, Pathology. Used to classify FMR1 CGG repeats as normal, intermediate, premutation, or full mutation for disease severity assessment.
When is CPT 81244 used?
Used to classify FMR1 CGG repeats as normal, intermediate, premutation, or full mutation for disease severity assessment.
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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.