CPT codes and LOINC update: November 2022

December 2, 2022

The following list includes updates posted to mayocliniclabs.com during the month of November:

CPT Code and Test Classification Updates

Test ID	Test Name	Updated
FHV8P 75756	Herpesvirus 8 (HHV-8) DNA, Quantitative Real-Time PCR Test Classification	11/21/2022 10:04am
FHHV6 91311	Herpes Virus 6 (HHV-6) DNA, Qualitative Real-Time PCR Test Classification	11/21/2022 10:01am
ANCA 9441	Cytoplasmic Neutrophil Antibodies, Serum CPT Code Information	11/15/2022 8:00pm
PCDES 605129	Pediatric Autoimmune Encephalopathy/CNS Disorder Evaluation, Serum CPT Code Information	11/11/2022 3:04pm
BRFKT 616786	BRAF/KIT Mutation Analysis, Next-Generation Sequencing, Tumor CPT Code Information	11/07/2022 3:05pm
ALAGP 618030	Alagille Syndrome Gene Panel, Varies CPT Code Information	11/07/2022 3:05pm
COMCP 614319	Hereditary Common Cancer Panel, Varies CPT Code Information	11/07/2022 3:05pm
CSFP 608336	Carrier Screen, Focused Panel, Varies CPT Code Information	11/07/2022 3:05pm
NEPHP 618086	Comprehensive Nephrology Gene Panel, Varies CPT Code Information	11/07/2022 10:05am
TCGR 83122	T-Cell Receptor Gene Rearrangement, PCR, Blood CPT Code Information	11/07/2022 10:01am
RSCGP 618128	Nephrocalcinosis, Nephrolithiasis, and Renal Electrolyte Imbalance Gene Panel, Varies CPT Code Information	11/04/2022 8:04pm
NEPHP 618086	Comprehensive Nephrology Gene Panel, Varies CPT Code Information	11/04/2022 8:04pm
RFSGS 618114	Focal Segmental Glomerulosclerosis (FSGS) and Nephrotic Syndrome Gene Panel, Varies CPT Code Information	11/04/2022 8:04pm
RBART 618100	Bartter Syndrome Gene Panel, Varies CPT Code Information	11/04/2022 8:04pm
CKDGP 618072	Cystic Kidney Disease Gene Panel, Varies CPT Code Information	11/04/2022 8:04pm
HMEP 616524	Hemiplegic Migraine With or Without Epilepsy Gene Panel, Varies CPT Code Information	11/04/2022 8:04pm
TSCP 616537	Tuberous Sclerosis Gene Panel, Varies CPT Code Information	11/04/2022 8:04pm
KRASW 616452	KRAS Somatic Mutation Analysis, Peritoneal Fluid CPT Code Information	11/04/2022 8:04pm
WILMP 614577	Hereditary Wilms Tumor Panel, Varies CPT Code Information	11/04/2022 8:04pm
XCP 614318	Hereditary Expanded Cancer Panel, Varies CPT Code Information	11/04/2022 8:04pm
BRGYP 614320	Hereditary Breast/Gynecologic Cancer Panel, Varies CPT Code Information	11/04/2022 8:04pm
LYNCP 614572	Lynch Syndrome Panel, Varies CPT Code Information	11/04/2022 8:04pm
PANCP 614574	Hereditary Pancreatic Cancer Panel, Varies CPT Code Information	11/04/2022 8:04pm
PRS8P 614576	Hereditary Prostate Cancer Panel, Varies CPT Code Information	11/04/2022 8:04pm
RENCP 614575	Hereditary Renal Cancer Panel, Varies CPT Code Information	11/04/2022 8:04pm
THYRP 614580	Hereditary Thyroid Cancer Panel, Varies CPT Code Information	11/04/2022 8:04pm
CFSMN 608349	Cystic Fibrosis and Spinal Muscular Atrophy Carrier Screen Panel, Varies CPT Code Information	11/04/2022 8:04pm
SCAP 609505	Spinocerebellar Ataxia Repeat Expansion Panel, Varies CPT Code Information	11/04/2022 8:04pm
CFMP 605197	Cystic Fibrosis, CFTR Gene, Variant Panel, Varies CPT Code Information	11/04/2022 8:04pm
PSYQP 610060	Psychotropic Pharmacogenomics Gene Panel, Varies CPT Code Information	11/04/2022 8:04pm
MSUDP 608031	Maple Syrup Urine Disease Gene Panel, Varies CPT Code Information	11/04/2022 8:04pm
PHEGP 608032	Phenylalanine Disorders Gene Panel, Varies CPT Code Information	11/04/2022 8:04pm
TYRGP 608033	Tyrosine Disorders Gene Panel, Varies CPT Code Information	11/04/2022 8:04pm
PCGP 608023	Porphyria Comprehensive Gene Panel, Varies CPT Code Information	11/04/2022 8:04pm
CLADP 608019	Congenital Lactic Acidosis Panel, Varies CPT Code Information	11/04/2022 8:04pm
APGP 608015	Acute Porphyria Gene Panel, Varies CPT Code Information	11/04/2022 8:04pm
HHLP 606144	AudioloGene Hereditary Hearing Loss Panel, Varies CPT Code Information	11/04/2022 8:04pm
EDSGP 65749	Ehlers-Danlos Syndrome Panel (12 Genes), Next-Generation Sequencing and Deletion/Duplication Analysis, Varies CPT Code Information	11/04/2022 8:03pm
FHRGP 65748	Familial Hypercholesterolemia and Related Disorders Multi-Gene Panel, Next-Generation Sequencing, Varies CPT Code Information	11/04/2022 8:03pm
KRASD 68003	Cell-Free DNA KRAS 12, 13, 61,146, Blood CPT Code Information	11/04/2022 8:03pm
NGCDA 64924	Congenital Dyserythropoietic Anemia Panel, Next-Generation Sequencing, Varies CPT Code Information	11/04/2022 8:03pm
NGMEM 64938	Red Blood Cell Membrane Panel, Next-Generation Sequencing, Varies CPT Code Information	11/04/2022 8:03pm
CYPZ 37445	21-Hydroxylase Gene, CYP21A2, Full Gene Analysis, Varies CPT Code Information	11/04/2022 8:03pm
MITOP 62510	Mitochondrial Full Genome Analysis, Next-Generation Sequencing (NGS), Varies CPT Code Information	11/04/2022 8:02pm
HPPAN 35640	Hereditary Pancreatitis Panel, Varies CPT Code Information	11/04/2022 8:02pm
TCGR 83122	T-Cell Receptor Gene Rearrangement, PCR, Blood CPT Code Information	11/04/2022 8:01pm
TCGBM 31139	T-Cell Receptor Gene Rearrangement, PCR, Bone Marrow CPT Code Information	11/04/2022 8:01pm
TCGRV 31140	T-Cell Receptor Gene Rearrangement, PCR, Varies CPT Code Information	11/04/2022 8:01pm
FLT 19739	FLT3 Mutation Analysis, Varies CPT Code Information	11/04/2022 8:01pm
HHTGP 65747	Hereditary Hemorrhagic Telangiectasia Gene Panel, Varies CPT Code Information	11/04/2022 3:04pm
BRGGP 63163	Brugada Syndrome Multi-Gene Panel, Blood CPT Code Information	11/04/2022 3:02pm
FLEP 91339	Leptin Test Classification	11/03/2022 3:01pm

LOINC Updates

Logical Observation Identifiers Names and Codes (LOINC^®) is clinical terminology that is important for laboratory test orders and results, and is one of a suite of designated standards for use in U.S. federal government systems for the electronic exchange of clinical health information.

Mayo Clinic Laboratories systematically assigns LOINC values to its assays, as provided in the following spreadsheet.

View the updated LOINC spreadsheet.

CPT codes and LOINC update: November 2022

CPT Code and Test Classification Updates

LOINC Updates

Michael Hutchison

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