81441 Ibmfs seq alys pnl 30 genes
Also known as: inherited bone marrow failure panel, IBMFS genetics, aplastic anemia genetics
Genetic sequence analysis panel for inherited bone marrow failure syndromes including 30 genes.
In Plain Language
genetic test for bone marrow failure; inherited blood cell disorder test
Clinical Context
Identifies genetic mutations causing Fanconi anemia, dyskeratosis congenita, and other inherited bone marrow failure syndromes.
RVU Information
CPT 81441 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 81441?
CPT 81441 (Ibmfs seq alys pnl 30 genes) is a Pathology & Lab code. Genetic sequence analysis panel for inherited bone marrow failure syndromes including 30 genes.
Who uses CPT code 81441?
CPT 81441 is used by hematology, genetics, molecular pathology. Identifies genetic mutations causing Fanconi anemia, dyskeratosis congenita, and other inherited bone marrow failure syndromes.
When is CPT 81441 used?
Identifies genetic mutations causing Fanconi anemia, dyskeratosis congenita, and other inherited bone marrow failure syndromes.
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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.