S3849 Gene test niemann-pick
Also known as: Niemann-Pick disease testing, lysosomal storage disorder gene test
Genetic testing for mutations in genes associated with Niemann-Pick disease types A, B, and C, lysosomal storage disorders.
In Plain Language
genetic test for rare storage disease; Niemann-Pick gene screening
Clinical Context
Used in pediatrics and medical genetics for diagnosis of Niemann-Pick disease in symptomatic patients or carrier screening.
RVU Information
CPT S3849 does not have a physician work RVU assigned by CMS. This is typical for supply, drug, and equipment codes — reimbursement is based on Average Sales Price (ASP), fee schedules, or payer contracts rather than the RVU system.
Billing & Documentation
S-codes are used by private payers (not Medicare) for services without a standard CPT or HCPCS code. Coverage varies significantly between insurers. Verify payer acceptance before billing and document medical necessity thoroughly.
Specialties
Frequently Asked Questions
What is CPT code S3849?
CPT S3849 (Gene test niemann-pick) is a S Codes code. Genetic testing for mutations in genes associated with Niemann-Pick disease types A, B, and C, lysosomal storage disorders.
Is S3849 covered by insurance?
S3849 is a temporary HCPCS code. Coverage varies by payer and may change when permanent codes are assigned. Used in pediatrics and medical genetics for diagnosis of Niemann-Pick disease in symptomatic patients or carrier screening.
When is CPT S3849 used?
Used in pediatrics and medical genetics for diagnosis of Niemann-Pick disease in symptomatic patients or carrier screening.
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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.