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Test ID: FIXMS    
Hemophilia B, F9 Gene Mutation Analysis, Whole Blood

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Test Classification Provides information regarding the medical device classification for laboratory test kits and reagents. Tests may be classified as cleared or approved by the US Food and Drug Administration (FDA) and used per manufacturer's instructions, or as products that do not undergo full FDA review and approval, and are then labeled as an Analyte Specific Reagent (ASR), Investigation Use Only (IUO) product, or a Research Use Only (RUO) product.

This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. This test has not been cleared or approved by the U.S. Food and Drug Administration.

CPT Code Information Provides guidance in determining the appropriate Current Procedural Terminology (CPT) code(s) information for each test or profile. The listed CPT codes reflect Mayo Medical Laboratories interpretation of CPT coding requirements. It is the responsibility of each laboratory to determine correct CPT codes to use for billing.

81405-F9 (coagulation factor IX) (eg, hemophilia B), full gene sequence

LOINC® Code Information Provides guidance in determining the Logical Observation Identifiers Names and Codes (LOINC) values for the order and result codes of this test.

Test IDTest Order NameOrder LOINC Code
FIXMSHemophilia B, F9 Gene Mutation Analysis, Whole BloodIn Process

 

Result IDTest Result NameResult LOINC Code
23776F9 Mut Screen Reason for Referral42349-1
23777F9 Mutation Screen Method49549-9
23778F9 Mutation Screen Result38896-7
23779F9 Mutation Screen Interpretation69049-5
37319F9 Mutation Screen Specimen TypeIn Process
23781F9 Mutation Screen Reviewed ByNo LOINC Needed

LOINC and CPT codes are provided by the performing laboratory.


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