81183 Atxn10 gene detc abnor allel
Also known as: ATXN10 repeat analysis, Spinocerebellar Ataxia 10 testing
Molecular analysis of the ATXN10 gene to detect abnormal ATTCT repeat expansions associated with Spinocerebellar Ataxia type 10.
In Plain Language
ataxia gene test; neurological disorder genetic testing
Clinical Context
Used to diagnose Spinocerebellar Ataxia type 10 in patients with progressive ataxia, seizures, and family history of similar neurological disease.
RVU Information
CPT 81183 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 81183?
CPT 81183 (Atxn10 gene detc abnor allel) is a Pathology & Lab code. Molecular analysis of the ATXN10 gene to detect abnormal ATTCT repeat expansions associated with Spinocerebellar Ataxia type 10.
Who uses CPT code 81183?
CPT 81183 is used by Genetics, Neurology, Pathology. Used to diagnose Spinocerebellar Ataxia type 10 in patients with progressive ataxia, seizures, and family history of similar neurological disease.
When is CPT 81183 used?
Used to diagnose Spinocerebellar Ataxia type 10 in patients with progressive ataxia, seizures, 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.