81182 Atxn8os gen detc abnor allel
Also known as: ATXN8OS repeat analysis, Spinocerebellar Ataxia 8 testing
Molecular analysis of the ATXN8OS gene to detect abnormal CAG repeat expansions associated with Spinocerebellar Ataxia type 8.
In Plain Language
ataxia gene test; neurological disorder genetic screening
Clinical Context
Ordered to diagnose Spinocerebellar Ataxia type 8 in patients with progressive cerebellar ataxia and family history of similar neurological disease.
RVU Information
CPT 81182 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 81182?
CPT 81182 (Atxn8os gen detc abnor allel) is a Pathology & Lab code. Molecular analysis of the ATXN8OS gene to detect abnormal CAG repeat expansions associated with Spinocerebellar Ataxia type 8.
Who uses CPT code 81182?
CPT 81182 is used by Genetics, Neurology, Pathology. Ordered to diagnose Spinocerebellar Ataxia type 8 in patients with progressive cerebellar ataxia and family history of similar neurological disease.
When is CPT 81182 used?
Ordered to diagnose Spinocerebellar Ataxia type 8 in patients with progressive cerebellar ataxia and family history of similar neurological disease.
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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.