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Test ID: NGAML    
Next-Generation Sequencing, Acute Myeloid Leukemia, 11-Gene Panel, Varies

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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 instructions, or as products that do not undergo full FDA review and approval, and are then labeled as an Analyte Specific Reagent (ASR) 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 Clinic Laboratories interpretation of CPT coding requirements. It is the responsibility of each laboratory to determine correct CPT codes to use for billing.

CPT codes are provided by the performing laboratory.

81450

LOINC® Information Provides guidance in determining the Logical Observation Identifiers Names and Codes (LOINC) values for the order and results codes of this test. LOINC values are provided by the performing laboratory.

Test IDTest Order NameOrder LOINC Value
NGAMLNext Gen Sequencing, AML, 11 GeneIn Process

 

Result IDTest Result NameResult LOINC ValueApplies only to results expressed in units of measure originally reported by the performing laboratory. These values do not apply to results that are converted to other units of measure.
MP038Specimen Type31208-2
43554NGAML ResultNo LOINC Needed
43488Pathogenic Mutations Detected41103-3
43487Interpretation69047-9
43489Clinical Trials82786-5
43490Variants of Unknown Significance82939-0
43491Additional Notes48767-8
43492Method Summary49549-9
43493Disclaimer62364-5
43494AML Panel Gene List36908-2
43495Reviewed By19139-5