"Listed on this spreadsheet are the Medicare Advisory Panel on Clinical Diagnostic Laboratory Tests (the Panel) recommendations to CMS and their votes for clinical diagnostic laboratory test codes for which CMS received no applicable information during the data reporting period from May 1, 2026 through July 31, 2026. These codes were presented and discussed at the Clinical Laboratory Fee Schedule (CLFS) public meeting that includes the Panel on the September 15 and 16, 2026.* Section 1834A(f)(1) of the Act provides authority for the Panel to advise and provide recommendations to CMS on the establishment of payment rates for clinical diagnostic laboratory tests, including whether to use crosswalking or gapfilling processes. As such, these are recommendations from the Panel, and are NOT the preliminary determinations from CMS, which are forthcoming.  The Panel considered recommendations from laboratories and stakeholders for every HCPCS code.  The codes were then grouped by common sub-committee recommendations, which informed each consent agenda.  CPT 0031U has been removed from this list following confirmation of its deletion by the AMA CPT.
* Link to list of codes reviewed by the Panel: https://www.cms.gov/files/document/consent-agenda-codes-cdlt-panel-meeting-9-16-2026.pdf 

Note, if the Panel recommends gapfill, their recommendation is that the CDLT begin a new gapfill process beginning January 1, 2027 and a national rate would be established January 1, 2028, "								
No.	Code	Long Code Descriptor	Panel Recommendation	Panel Votes				
1	0007U	"Drug test(s), presumptive, with definitive confirmation of positive results, any number of drug classes, urine, includes specimen verification including dna authentication in comparison to buccal dna, per date of service"	"Crosswalk to G0480
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
2	0011M	"Oncology, prostate cancer, mrna expression assay of 12 genes (10 content and 2 housekeeping), rt-pcr test utilizing blood plasma and urine, algorithms to predict high-grade prostate cancer risk"	"Crosswalk to 0005U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
3	0017M	"Oncology (diffuse large b-cell lymphoma [dlbcl]), mrna, gene expression profiling by fluorescent probe hybridization of 20 genes, formalin-fixed paraffin-embedded tissue, algorithm reported as cell of origin"	"Crosswalk to 0120U
Gapfill
Abstain"	"10 out of 11
0 out of 11
1 out of 11"				
4	0017U	"Oncology (hematolymphoid neoplasia), jak2 mutation, dna, pcr amplification of exons 12-14 and sequence analysis, blood or bone marrow, report of jak2 mutation not detected or detected"	"Crosswalk to 81270
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
5	0025U	"Tenofovir, by liquid chromatography with tandem mass spectrometry (lc-ms/ms), urine, quantitative"	"Crosswalk to G0480
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
6	0032U	"Comt (catechol-o-methyltransferase) (drug metabolism) gene analysis, c.472g>a (rs4680) variant"	"Crosswalk to 81230
Crosswalk to 81227+81355
Gapfill
Abstain"	"10 out of 11
0 out of 11
0 out of 11
1 out of 11"				
7	0036U	"Exome (ie, somatic mutations), paired formalin-fixed paraffin-embedded tumor tissue and normal specimen, sequence analyses"	"Crosswalk to 81415
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
8	0039U	"Deoxyribonucleic acid (dna) antibody, double stranded, high avidity"	"Crosswalk to 86225
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
9	0040U	"Bcr/abl1 (t(9;22)) (eg, chronic myelogenous leukemia) translocation analysis, major breakpoint, quantitative"	"Crosswalk to 81206 x 2.5
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
10	0051U	"Prescription drug monitoring, evaluation of drugs present by liquid chromatography tandem mass spectrometry (lc-ms/ms), urine or blood, 31 drug panel, reported as quantitative results, detected or not detected, per date of service"	"Crosswalk to G0483
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
11	0052U	"Lipoprotein, blood, high resolution fractionation and quantitation of lipoproteins, including all five major lipoprotein classes and subclasses of hdl, ldl, and vldl by vertical auto profile ultracentrifugation"	"Crosswalk to 83701
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
12	0054U	"Prescription drug monitoring, 14 or more classes of drugs and substances, definitive tandem mass spectrometry with chromatography, capillary blood, quantitative report with therapeutic and toxic ranges, including steady-state range for the prescribed dose when detected, per date of service"	"Crosswalk to G0482
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
13	0061U	"Transcutaneous measurement of five biomarkers (tissue oxygenation [sto2], oxyhemoglobin [cthbo2], deoxyhemoglobin [cthbr], papillary and reticular dermal hemoglobin concentrations [cthb1 and cthb2]), using spatial frequency domain imaging (sfdi) and multi-spectral analysis"	"Crosswalk to 88738 x 5
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
14	0069U	"Oncology (colorectal), microrna, rt-pcr expression profiling of mir-31-3p, formalin-fixed paraffin-embedded tissue, algorithm reported as an expression sco"	"Crosswalk to 0005U x 0.5
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
15	0093U	"Prescription drug monitoring, evaluation of 65 common drugs by lc-ms/ms, urine, each drug reported detected or not detected"	"Crosswalk to 80307
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
16	0096U	"Human papillomavirus (hpv), high-risk types (ie, 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, 68), male urine"	"Crosswalk to 87624
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
17	0107U	"Clostridium difficile toxin(s) antigen detection by immunoassay technique, stool, qualitative, multiple-step method"	"Crosswalk to 87803
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
18	0110U	"Prescription drug monitoring, one or more oral oncology drug(s) and substances, definitive tandem mass spectrometry with chromatography, serum or plasma from capillary blood or venous blood, quantitative report with steady-state range for the prescribed drug(s) when detected"	"Crosswalk to 80199
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
19	0111U	"Oncology (colon cancer), targeted kras (codons 12, 13, and 61) and nras (codons 12, 13, and 61) gene analysis utilizing formalin-fixed paraffin-embedded tissue"	"Crosswalk to 81275+ 81276+ 81311
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
20	0113U	"Oncology (prostate), measurement of pca3 and tmprss2-erg in urine and psa in serum following prostatic massage, by rna amplification and fluorescencebased detection, algorithm reported as risk score"	"Crosswalk to 0005U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
21	0130U	"Hereditary colon cancer disorders (eg, lynch syndrome, pten hamartoma syndrome, cowden syndrome, familial adenomatosis polyposis), targeted mrna sequence analysis panel (apc, cdh1, chek2, mlh1, msh2, msh6, mutyh, pms2, pten, and tp53) (list separately in addition to code for primary procedure)"	"Crosswalk to 81435
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
22	0154U	"Oncology (urothelial cancer), rna,analysis by real-time rt-pcr of the fgfr3 (fibroblast growth factor receptor 3) gene analysis (ie, p.r248c [c.742c>t], p.s249c [c.746c>g], p.g370c [c.1108g>t], p.y373c [c.1118a>g], fgfr3-tacc3v1, and fgfr3-tacc3v3) utilizing formalin-fixed paraffin-embedded urothelial cancer tumor tissue, reported as fgfr gene alteration status"	"Crosswalk to 81309+ 81315
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
23	0166U	"Liver disease, 10 biochemical assays (a2-macroglobulin, haptoglobin, apolipoprotein a1, bilirubin, ggt, alt, ast, triglycerides, cholesterol, fasting glucose) and biometric and demographic data, utilizing serum, algorithm reported as scores for fibrosis, necroinflammatory activity, and steatosis with a summary interpretation"	"Crosswalk to 0003M
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
24	0169U	"Nudt15 (nudix hydrolase 15) and tpmt (thiopurine s-methyltransferase) (eg, drug metabolism) gene analysis, common variants"	"Crosswalk to 0034U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
25	0176U	"Cytolethal distending toxin b (cdtb) and vinculin igg antibodies by immunoassay (ie, elisa)"	"Crosswalk to 86828
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
26	0177U	"Oncology (breast cancer), dna, pik3ca (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha) gene analysis of 11 gene variants utilizing plasma, reported as pik3ca gene mutation status"	"Crosswalk to 81309
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
27	0181U	"Red cell antigen (colton blood group) genotyping (co), gene analysis, aqp1 (aquaporin 1 [colton blood group]) exon 1"	"Crosswalk to 81403
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
28	0182U	"Red cell antigen (cromer blood group) genotyping (crom), gene analysis, cd55 (cd55 molecule [cromer blood group]) exons 1-10"	"Crosswalk to 81405
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
29	0183U	"Red cell antigen (diego blood group) genotyping (di), gene analysis, slc4a1 (solute carrier family 4 member 1 [diego blood group]) exon 19"	"Crosswalk to 81403
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
30	0184U	"Red cell antigen (dombrock blood group) genotyping (do), gene analysis, art4 (adp-ribosyltransferase 4 [dombrock blood group]) exon 2"	"Crosswalk to 81403
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
31	0185U	"Red cell antigen (h blood group) genotyping (fut1), gene analysis, fut1 (fucosyltransferase 1 [h blood group]) exon 4"	"Crosswalk to 81403
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
32	0186U	"Red cell antigen (h blood group) genotyping (fut2), gene analysis, fut2 (fucosyltransferase 2) exon 2"	"Crosswalk to 81403
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
33	0187U	"Red cell antigen (duffy blood group) genotyping (fy), gene analysis, ackr1 (atypical chemokine receptor 1 [duffy blood group]) exons 1-2"	"Crosswalk to 81404
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
34	0188U	"Red cell antigen (gerbich blood group) genotyping (ge), gene analysis, gypc (glycophorin c [gerbich blood group]) exons 1-4"	"Crosswalk to 81404
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
35	0189U	"Red cell antigen (mns blood group) genotyping (gypa), gene analysis, gypa (glycophorin a [mns blood group]) introns 1, 5, exon 2"	"Crosswalk to 81404
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
36	0190U	"Red cell antigen (mns blood group) genotyping (gypb), gene analysis, gypb (glycophorin b [mns blood group]) introns 1, 5, pseudoexon 3"	"Crosswalk to 81404
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
37	0191U	"Red cell antigen (indian blood group) genotyping (in), gene analysis, cd44 (cd44 molecule [indian blood group]) exons 2, 3, 6"	"Crosswalk to 81404
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
38	0192U	"Red cell antigen (kidd blood group) genotyping (jk), gene analysis, slc14a1 (solute carrier family 14 member 1 [kidd blood group]) gene promoter, exon 9"	"Crosswalk to 81404
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
39	0193U	"Red cell antigen (jr blood group) genotyping (jr), gene analysis, abcg2 (atp binding cassette subfamily g member 2 [junior blood group]) exons 2-26"	"Crosswalk to 81406
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
40	0194U	"Red cell antigen (kell blood group) genotyping (kel), gene analysis, kel (kell metallo-endopeptidase [kell blood group]) exon 8"	"Crosswalk to 81403
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
41	0195U	"Klf1 (kruppel-like factor 1), targeted sequencing (ie, exon 13)"	"Crosswalk to 81215
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
42	0196U	"Red cell antigen (lutheran blood group) genotyping (lu), gene analysis, bcam (basal cell adhesion molecule [lutheran blood group]) exon 3"	"Crosswalk to 81403
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
43	0197U	"Red cell antigen (landsteiner-wiener blood group) genotyping (lw), gene analysis, icam4 (intercellular adhesion molecule 4 [landsteiner-wiener blood group]) exon 1"	"Crosswalk to 81403
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
44	0198U	"Red cell antigen (rh blood group) genotyping (rhd and rhce), gene analysis sanger/chain termination/conventional sequencing, rhd (rh blood group d antigen) exons 1-10 and rhce (rh blood group ccee antigens) exon 5"	"Crosswalk to 81406
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
45	0199U	"Red cell antigen (scianna blood group) genotyping (sc), gene analysis, ermap (erythroblast membrane associated protein [scianna blood group]) exons 4, 12"	"Crosswalk to 81404
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
46	0200U	"Red cell antigen (kx blood group) genotyping (xk), gene analysis, xk (x-linked kx blood group) exons 1-3"	"Crosswalk to 81404
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
47	0201U	"Red cell antigen (yt blood group) genotyping (yt), gene analysis, ache (acetylcholinesterase [cartwright blood group]) exon 2"	"Crosswalk to 81403
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
48	0203U	"Autoimmune (inflammatory bowel disease), mrna, gene expression profiling by quantitative rt-pcr, 17 genes (15 target and 2 reference genes), whole blood, reported as a continuous risk score and classification of inflammatory bowel disease aggressiveness"	"Crosswalk to 0005U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
49	0205U	"Ophthalmology (age-related macular degeneration), analysis of 3 gene variants (2 cfh gene, 1 arms2 gene), using pcr and maldi-tof, buccal swab, reported as positive or negative for neovascular age-related macular-degeneration risk associated with zinc supplements"	"Crosswalk to 81330
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
50	0209U	"Cytogenomic constitutional (genome-wide) analysis, interrogation of genomic regions for copy number, structural changes and areas of homozygosity for chromosomal abnormalities"	"Crosswalk to 81229
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
51	0218U	"Neurology (muscular dystrophy), dmd gene sequence analysis, including small sequence changes, deletions, duplications, and variants in non-uniquely mappable regions, blood or saliva, identification and characterization of genetic variants"	"Crosswalk to 0218U
Crosswalk to 81408+ 81161
Gapfill
Abstain"	"0 out of 11
11 out of 11
0 out of 11
0 out of 11"				
52	0227U	"Drug assay, presumptive, 30 or more drugs or metabolites, urine, liquid chromatography with tandem mass spectrometry (lc-ms/ms) using multiple reaction monitoring (mrm), with drug or metabolite description, includes sample validation"	"Crosswalk to 80307
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
53	0229U	"Bcat1 (branched chain amino acid transaminase 1) and ikzf1 (ikaros family zinc finger 1) (eg, colorectal cancer) promoter methylation analysis"	"Crosswalk to 81327 x 2
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
54	0230U	"Ar (androgen receptor) (eg, spinal and bulbar muscular atrophy, kennedy disease, x chromosome inactivation), full sequence analysis, including small sequence changes in exonic and intronic regions, deletions, duplications, short tandem repeat (str) expansions, mobile element insertions, and variants in non-uniquely mappable regions"	"Crosswalk to 81173
Crosswalk to 0230U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11
0 out of 11"				
55	0231U	"Cacna1a (calcium voltage-gated channel subunit alpha 1a) (eg, spinocerebellar ataxia), full gene analysis, including small sequence changes in exonic and intronic regions, deletions, duplications, short tandem repeat (str) gene expansions, mobile element insertions, and variants in non-uniquely mappable regions"	"Crosswalk to 81185
Crosswalk to 0231U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11
0 out of 11"				
56	0232U	"Cstb (cystatin b) (eg, progressive myoclonic epilepsy type 1a, unverricht-lundborg disease), full gene analysis, including small sequence changes in exonic and intronic regions, deletions, duplications, short tandem repeat (str) expansions, mobile element insertions, and variants in non-uniquely mappable regions"	"Crosswalk to 81189
Crosswalk to 0232U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11
0 out of 11"				
57	0233U	"Fxn (frataxin) (eg, friedreich ataxia), gene analysis, including small sequence changes in exonic and intronic regions, deletions, duplications, short tandem repeat (str) expansions, mobile element insertions, and variants in non-uniquely mappable regions"	"Crosswalk to 81286
Crosswalk to 0233U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11
0 out of 11"				
58	0234U	"Mecp2 (methyl cpg binding protein 2) (eg, rett syndrome), full gene analysis, including small sequence changes in exonic and intronic regions, deletions, duplications, mobile element insertions, and variants in non-uniquely mappable regions"	"Crosswalk to 81302
Crosswalk to 0234U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11
0 out of 11"				
59	0235U	"Pten (phosphatase and tensin homolog) (eg, cowden syndrome, pten hamartoma tumor syndrome), full gene analysis, including small sequence changes in exonic and intronic regions, deletions, duplications, mobile element insertions, and variants in non-uniquely mappable regions"	"Crosswalk to 81321
Crosswalk to 0235U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11
0 out of 11"				
60	0236U	"Smn1 (survival of motor neuron 1, telomeric) and smn2 (survival of motor neuron 2, centromeric) (eg, spinal muscular atrophy) full gene analysis, including small sequence changes in exonic and intronic regions, duplications and deletions, and mobile element insertions"	"Crosswalk to 81336+ 81405
Crosswalk to 0236U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11
0 out of 11"				
61	0237U	"Cardiac ion channelopathies (eg, brugada syndrome, long qt syndrome, short qt syndrome, catecholaminergic polymorphic ventricular tachycardia), genomic sequence analysis panel including ank2, casq2, cav3, kcne1, kcne2, kcnh2, kcnj2, kcnq1, ryr2, and scn5a, including small sequence changes in exonic and intronic regions, deletions, duplications, mobile element insertions, and variants in non-uniquely mappable regions"	"Crosswalk to 81413
Crosswalk to 0237U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11
0 out of 11"				
62	0238U	"Oncology (lynch syndrome), genomic dna sequence analysis of mlh1, msh2, msh6, pms2, and epcam, including small sequence changes in exonic and intronic regions, deletions, duplications, mobile element insertions, and variants in non-uniquely mappable regions"	"Crosswalk to 81435
Crosswalk to 0238U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11
0 out of 11"				
63	0246U	"Red blood cell antigen typing, dna, genotyping of at least 16 blood groups with phenotype prediction of at least 51 red blood cell antigens"	"Crosswalk to 0001U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
64	0259U	"Nephrology (chronic kidney disease), nuclear magnetic resonance spectroscopy measurement of myo-inositol, valine, and creatinine, algorithmically combined with cystatin c (by immunoassay) and demographic data to determine estimated glomerular filtration rate (gfr), serum, quantitative"	"Crosswalk to 83704+ 82610
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
65	0275U	"Hematology (heparin-induced thrombocytopenia), platelet antibody reactivity by flow cytometry, serum"	"Crosswalk to 86022
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
66	0287U	"Oncology (thyroid), dna and mrna, next-generation sequencing analysis of 112 genes, fine needle aspirate or formalin-fixed paraffin-embedded (ffpe) tissue, algorithmic prediction of cancer recurrence, reported as a categorical risk result (low, intermediate, high)"	"Crosswalk to 0026U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
67	0289U	"Neurology (alzheimer disease), mrna, gene expression profiling by rna sequencing of 24 genes, whole blood, algorithm reported as predictive risk score"	"Crosswalk to 0005U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
68	0290U	"Pain management, mrna, gene expression profiling by rna sequencing of 36 genes, whole blood, algorithm reported as predictive risk score"	"Crosswalk to 0005U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
69	0293U	"Psychiatry (suicidal ideation), mrna, gene expression profiling by rna sequencing of 54 genes, whole blood, algorithm reported as predictive risk score"	"Crosswalk to 0005U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
70	0294U	"Longevity and mortality risk, mrna, gene expression profiling by rna sequencing of 18 genes, whole blood, algorithm reported as predictive risk score"	"Crosswalk to 0005U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
71	0298U	"Oncology (pan tumor), whole transcriptome sequencing of paired malignant and normal rna specimens, fresh or formalin-fixed paraffin-embedded (ffpe) tissue, blood or bone marrow, comparative sequence analyses and expression level and chimeric transcript identification"	"Crosswalk to 81455
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
72	0316U	"Borrelia burgdorferi (lyme disease), ospa protein evaluation, urine"	"Crosswalk to 87449+ 87015
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
73	0321U	"Infectious agent detection by nucleic acid (dna or rna), genitourinary pathogens, identification of 20 bacterial and fungal organisms and identification of 16 associated antibiotic-resistance genes, multiplex amplified probe technique"	"Crosswalk to 87632+ 87633
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
74	0323U	"Infectious agent detection by nucleic acid (dna and rna), central nervous system pathogen, metagenomic next-generation sequencing, cerebrospinal fluid (csf), identification of pathogenic bacteria, viruses, parasites, or fungi"	"Crosswalk to 0152U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
75	0327U	"Fetal aneuploidy (trisomy 13, 18, and 21), dna sequence analysis of selected regions using maternal plasma, algorithm reported as a risk score for each trisomy, includes sex reporting, if performed"	"Crosswalk to 81420
Crosswalk to 0327U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11
0 out of 11"				
76	0342U	"Oncology (pancreatic cancer), multiplex immunoassay of c5, c4, cystatin c, factor b, osteoprotegerin (opg), gelsolin, igfbp3, ca125 and multiplex electrochemiluminescent immunoassay (eclia) for ca19-9, serum, diagnostic algorithm reported qualitatively as positive, negative, or borderline"	"Crosswalk to 81503
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
77	0343U	"Oncology (prostate), exosome-based analysis of 442 small noncoding rnas (sncrnas) by quantitative reverse transcription polymerase chain reaction (rt-qpcr), urine, reported as molecular evidence of no-, low-, intermediate- or high-risk of prostate cancer"	"Crosswalk to 0005U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
78	0362U	"Oncology (papillary thyroid cancer), gene-expression profiling via targeted hybrid capture-enrichment rna sequencing of 82 content genes and 10 housekeeping genes, fine needle aspirate or formalin-fixed paraffin embedded (ffpe) tissue, algorithm reported as one of three molecular subtypes"	"Crosswalk to 0026U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
79	0371U	"Infectious agent detection by nucleic acid (dna or rna), genitourinary pathogen, semiquantitative identification, dna from 16 bacterial organisms and 1 fungal organism, multiplex amplified probe technique via quantitative polymerase chain reaction (qpcr), urine"	"Crosswalk to 87633
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
80	0372U	"Infectious disease (genitourinary pathogens), antibiotic-resistance gene detection, multiplex amplified probe technique, urine, reported as an antimicrobial stewardship risk score"	"Crosswalk to 87633
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
81	0377U	"Cardiovascular disease, quantification of advanced serum or plasma lipoprotein profile, by nuclear magnetic resonance (nmr) spectrometry with report of a lipoprotein profile (including 23 variables)"	"Crosswalk to 83704+ 80061
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
82	0385U	"Nephrology (chronic kidney disease), apolipoprotein a4 (apoa4), cd5 antigen-like (cd5l), and insulin-like growth factor binding protein 3 (igfbp3) by enzyme-linked immunoassay (elisa), plasma, algorithm combining results with hdl, estimated glomerular filtration rate (gfr) and clinical data reported as a risk score for developing diabetic kidney disease"	"Crosswalk to 0308U
Gapfill
Abstain"	"10 out of 11
0 out of 11
1 out of 11"				
83	0387U	"Oncology (melanoma), autophagy and beclin 1 regulator 1 (ambra1) and loricrin (amlo) by immunohistochemistry, formalinfixed paraffin-embedded (ffpe) tissue, report for risk of progression"	"Crosswalk 0067U x 0.5 **( Update)
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
84	0394U	"Perfluoroalkyl substances (pfas) (eg, perfluorooctanoic acid, perfluorooctane sulfonic acid), 16 pfas compounds by liquid chromatography with tandem mass spectrometry (lc-ms/ms), plasma or serum, quantitative"	"Crosswalk to G0482
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
85	0405U	"Oncology (pancreatic), 59 methylation haplotype block markers, next-generation sequencing, plasma, reported as cancer signal detected or not detected"	"Crosswalk 0318U **(Update)
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
86	0409U	"Oncology (solid tumor), dna (80 genes) and rna (36 genes), by next-generation sequencing from plasma, including single nucleotide variants, insertions/deletions, copy number alterations, microsatellite instability, and fusions, report showing identified mutations with clinical actionability"	"Crosswalk to 81455
Gapfill
Abstain"	"10 out of 11
0 out of 11
1 out of 11"				
87	0421U	"Oncology (colorectal) screening, quantitative real-time target and signal amplification of 8 rna markers (gapdh, smad4, acy1, areg, cdh1, kras, tnfrsf10b, egln2) and fecal hemoglobin, algorithm reported as a positive or negative for colorectal cancer risk"	"Crosswalk to 81528
Crosswalk to 0464U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11
0 out of 11"				
88	0424U	"Oncology (prostate), exosome-based analysis of 53 small noncoding rnas (sncrnas) by quantitative reverse transcription polymerase chain reaction (rt-qpcr), urine, reported as no molecular evidence, low-, moderate- or elevated-risk of prostate cancer"	"Crosswalk to 0005U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
89	0427U	"Monocyte distribution width, whole blood (list separately in addition to code for primary procedure)"	"Crosswalk to 85049
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
90	0429U	"Human papillomavirus (hpv), oropharyngeal swab, 14 high-risk types (ie, 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, and 68)"	"Crosswalk to 87624
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
91	0437U	"Psychiatry (anxiety disorders), mrna, gene expression profiling by rna sequencing of 15 biomarkers, whole blood, algorithm reported as predictive risk score"	"Crosswalk to 0005U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
92	0442U	"Infectious disease (respiratory infection), myxovirus resistance protein a (mxa) and c-reactive protein (crp), fingerstick whole blood specimen, each biomarker reported as present or absent"	"Crosswalk to 87811 x 2
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
93	0444U	"Oncology (solid organ neoplasia), targeted genomic sequence analysis panel of 361 genes, interrogation for gene fusions, translocations, or other rearrangements, using dna from formalin-fixed paraffin-embedded (ffpe) tumor tissue, report of clinically significant variant(s)"	"Crosswalk to 81455
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
94	0452U	"Oncology (bladder), methylated penk dna detection by linear target enrichment-quantitative methylation-specific real-time pcr (lte-qmsp), urine, reported as likelihood of bladder cancer"	"Crosswalk to 81327
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
95	0453U	"Oncology (colorectal cancer), cellfree dna (cfdna), methylationbased quantitative pcr assay (septin9, ikzf1, bcat1, septin9-2, vav3, bcan), plasma, reported as presence or absence of circulating tumor dna (ctdna)"	"Crosswalk to 81327
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
96	0458U	"Oncology (breast cancer), s100a8 and s100a9, by enzymelinked immunosorbent assay (elisa), tear fluid with age, algorithm reported as a risk score"	"Crosswalk to 81500
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
97	0469U	"Rare diseases (constitutional/heritable disorders), whole genome sequence analysis for chromosomal abnormalities, copy number variants, duplications/deletions, inversions, unbalanced translocations, regions of homozygosity (roh), inheritance pattern that indicate uniparental disomy (upd), and aneuploidy, fetal sample (amniotic fluid, chorionic villus sample, or products of conception), identification and categorization of genetic variants, diagnostic report of fetal results based on phenotype with maternal sample and paternal sample, if performed, as comparators and/or maternal cell contamination"	"Crosswalk to 81229
Crosswalk to 0469U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11
0 out of 11"				
98	0494U	"Red blood cell antigen (fetal rhd gene analysis), next-generation sequencing of circulating cell-free dna (cfdna) of blood in pregnant individuals known to be rhd negative, reported as positive or negative"	"Crosswalk to 0494U
Crosswalk to 81422
Gapfill
Abstain"	"0 out of 11
11 out of 11
0 out of 11
0 out of 11"				
99	0495U	"Oncology (prostate), analysis of circulating plasma proteins (tpsa, fpsa, klk2, psp94, and gdf15), germline polygenic risk score (60 variants), clinical information (age, family history of prostate cancer, prior negative prostate biopsy), algorithm reported as risk of likelihood of detecting clinically significant prostate cancer"	"Crosswalk to 81539
Crosswalk to 0495U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11
0 out of 11"				
100	0497U	"Oncology (prostate), mrna geneexpression profiling by real-time rt-pcr of 6 genes (foxm1, mcm3, mtus1, ttc21b, alas1, and ppp2ca), utilizing formalinfixed paraffin-embedded (ffpe) tissue, algorithm reported as a risk score for prostate cancer"	"Crosswalk to 0047U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
101	0499U	"Oncology (colorectal and lung), dna from formalin-fixed paraffinembedded (ffpe) tissue, nextgeneration sequencing of 8 genes (nras, egfr, ctnnb1, pik3ca, apc, braf, kras, and tp53), mutation detection"	"Crosswalk to 81445
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
102	0500U	"Autoinflammatory disease (vexas syndrome), dna, uba1 gene mutations, targeted variant analysis (m41t, m41v, m41l, c.118-2a>c, c.118-1g>c, c.1189_118-2del, s56f, s621c)"	"Crosswalk to 81233
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
103	0502U	"Human papillomavirus (hpv), e6/e7 markers for high-risk types (16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, and 68), cervical cells, branched-chain capture hybridization, reported as negative or positive for high risk for hpv"	"Crosswalk to 87624
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
104	0504U	"Infectious disease (urinary tract infection), identification of 17 pathologic organisms, urine, realtime pcr, reported as positive or negative for each organism"	"Crosswalk to 87507
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
105	0505U	"Infectious disease (vaginal infection), identification of 32 pathogenic organisms, swab, real-time pcr, reported as positive or negative for each organism"	"Crosswalk to 87506+ 87507
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
106	0514U	"Gastroenterology (irritable bowel disease [ibd]), immunoassay for quantitative determination of adalimumab (adl) levels in venous serum in patients undergoing adalimumab therapy, results reported as a numerical value as micrograms per milliliter ( g/ml)"	"Crosswalk to 80145
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
107	0515U	"Gastroenterology (irritable bowel disease [ibd]), immunoassay for quantitative determination of infliximab (ifx) levels in venous serum in patients undergoing infliximab therapy, results reported as a numerical value as micrograms per milliliter ( g/ml)"	"Crosswalk to 80230
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
108	0517U	"Therapeutic drug monitoring, 80 or more psychoactive drugs or substances, lc-ms/ms, plasma, qualitative and quantitative therapeutic minimally and maximally effective dose of prescribed and non-prescribed medications"	"Crosswalk to G0483
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
109	0518U	"Therapeutic drug monitoring, 90 or more pain and mental health drugs or substances, lc-ms/ms, plasma, qualitative and quantitative therapeutic minimally effective range of prescribed and non-prescribed medications"	"Crosswalk to G0483
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
110	0519U	"Therapeutic drug monitoring, medications specific to pain, depression, and anxiety, lcms/ms, plasma, 110 or more drugs or substances, qualitative and quantitative therapeutic minimally effective range of prescribed, non-prescribed, and illicit medications in circulation"	"Crosswalk to G0483
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
111	0520U	"Therapeutic drug monitoring, 200 or more drugs or substances, lcms/ms, plasma, qualitative and quantitative therapeutic minimally effective range of prescribed and non-prescribed medications"	"Crosswalk to G0483
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
112	0521U	"Rheumatoid factor iga and igm, cyclic citrullinated peptide (ccp) antibodies, and scavenger receptor a (sr-a) by immunoassay, blood"	"Crosswalk to 86200 x 4
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
113	0527U	"Herpes simplex virus (hsv) types 1 and 2 and varicella zoster virus (vzv), amplified probe technique, each pathogen reported as detected or not detected"	"Crosswalk to 87631
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
114	0530U	"Oncology (pan-solid tumor), ctdna, utilizing plasma, next-generation sequencing (ngs) of 77 genes, 8 fusions, microsatellite instability, and tumor mutation burden, interpretative report for single-nucleotide variants, copy-number alterations, with therapy association"	"Crosswalk to 81455
Gapfill
Abstain"	"10 out of 11
0 out of 11
1 out of 11"				
115	0535U	"Perfluoroalkyl substances (pfas) (eg, perfluorooctanoic acid, perfluorooctane sulfonic acid), by liquid chromatography with tandem mass spectrometry (lcms/ms), plasma or serum, quantitative"	"Crosswalk to 80307
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
116	0536U	"Red blood cell antigen (fetal rhd), pcr analysis of exon 4 of rhd gene and housekeeping control gene gapdh from whole blood in pregnant individuals at 10+ weeks gestation known to be rhd negative, reported as fetal rhd status"	"Crosswalk to 81327
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
117	0538U	"Oncology (solid tumor), nextgeneration targeted sequencing analysis, formalin-fixed paraffinembedded (ffpe) tumor tissue, dna analysis of 600 genes, interrogation for single-nucleotide variants, insertions/deletions, gene rearrangements, and copy number alterations, microsatellite instability, tumor mutation burden, reported as actionable variant"	"Crosswalk to 81459
Crosswalk to 0334U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11
0 out of 11"				
118	0545U	"Acetylcholine receptor (achr), antibody identification by immunofluorescence, using live cells, reported as positive or negative"	"Crosswalk to 86363
Gapfill
Abstain"	"10 out of 11
0 out of 11
1 out of 11"				
119	0546U	"Low-density lipoprotein receptor-related protein 4 (lrp4), antibody identification by immunofluorescence, using live cells, reported as positive or negative"	"Crosswalk to 86363
Gapfill
Abstain"	"10 out of 11
0 out of 11
1 out of 11"				
120	0549U	"Oncology (urothelial), dna, quantitative methylated realtime pcr of trna-cys, sim2, and nkx1-1, using urine, diagnostic algorithm reported as a probability index for bladder cancer and/or upper tract urothelial carcinoma (utuc)"	"Crosswalk to 0012M
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
121	0557U	"Infectious disease (bacterial vaginosis and vaginitis), real-time amplification of dna markers for atopobium vaginae, gardnerella vaginalis, megasphaera types 1 and 2, bacterial vaginosis associated bacteria-2 and -3 (bvab-2, bvab-3), mobiluncus species, trichomonas vaginalis, neisseria gonorrhoeae, candida species (c. albicans, c. tropicalis, c. parapsilosis, c. glabrata, c. krusei), herpes simplex viruses 1 and 2, vaginal fluid, reported as detected or not detected for each organism"	"Crosswalk to 81514
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
122	0558U	"Oncology (colorectal), quantitative enzyme-linked immunosorbent assay (elisa) for secreted colorectal cancer protein marker (bf7 antigen), using serum, result reported as indicative of response/no response to therapy or disease progression/regression"	"Crosswalk to 86316
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
123	0559U	"Oncology (breast), quantitative enzyme-linked immunosorbent assay (elisa) for secreted breast cancer protein marker (bf9 antigen), serum, result reported as indicative of response/no response to therapy or disease progression/regression"	"Crosswalk to 86316
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
124	0563U	"Infectious disease (bacterial and/or viral respiratory tract infection), pathogen-specific nucleic acid (dna or rna), 11 viral targets and 4 bacterial targets, qualitative rt-pcr, upper respiratory specimen, each pathogen reported as positive or negative"	"Crosswalk to 87633
Crosswalk to 0563U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11
0 out of 11"				
125	0564U	"Infectious disease (bacterial and/or viral respiratory tract infection), pathogen-specific nucleic acid (dna or rna), 10 viral targets and 4 bacterial targets, qualitative rt-pcr, upper respiratory specimen, each pathogen reported as positive or negative"	"Crosswalk to 87633
Crosswalk to 0564U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11
0 out of 11"				
126	0568U	"Neurology (dementia), beta amyloid (ab40, ab42, ab42/40 ratio), tau-protein phosphorylated at residue (eg, ptau217), neurofilament light chain (nfl), and glial fibrillary acidic protein (gfap), by ultra-high sensitivity molecule array detection, plasma, algorithm reported as positive, intermediate, or negative for alzheimer pathology"	"Crosswalk to 81503
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
127	0570U	"Neurology (traumatic brain injury), analysis of glial fibrillary acidic protein (gfap) and ubiquitin carboxyl-terminal hydrolase l1 (uch-l1), immunoassay, whole blood or plasma, individual components reported with the overall result of elevated or non-elevated based on threshold comparison"	"Crosswalk to 81500
Crosswalk to 0570U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11
0 out of 11"				
128	0571U	"Oncology (solid tumor), dna (80 genes) and rna (10 genes), by next-generation sequencing, plasma, including single-nucleotide variants, insertions/deletions, copy-number alterations, microsatellite instability, and fusions, reported as clinically actionable variants"	"Crosswalk to 81455
Gapfill
Abstain"	"10 out of 11
0 out of 11
1 out of 11"				
129	0575U	"Transplantation medicine (liver allograft rejection), mirna gene expression profiling by rt-pcr of 4 genes (mir-122, mir-885, mir-23a housekeeping, spike-in control), serum, algorithm reported as risk of liver allograft rejection"	"Crosswalk to 0005U x 0.50
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
130	0576U	"Transplantation medicine (liver allograft rejection), quantitative donor-derived cell-free dna (cfdna) by whole genome nextgeneration sequencing, plasma and mrna gene expression profiling by multiplex real-time pcr of 56 genes, whole blood, combined algorithm reported as a rejection risk score"	"Crosswalk to 81595
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
131	0579U	"Nephrology (diabetic chronic kidney disease), enzymelinked immunosorbent assay (elisa) of apolipoprotein a4 (apoa4), cd5 antigen-like (cd5l) combined with estimated glomerular filtration rate (gfr), age, plasma, algorithm reported as a risk score for kidney function decline"	"Crosswalk to 0308U
Gapfill
Abstain"	"10 out of 11
0 out of 11
1 out of 11"				
132	0581U	"Transplantation medicine, antibody to non-human leukocyte antigens (nonhla), blood specimen, flow cytometry, single-antigen bead technology, 39 targets, individual positive antibodies reported"	"Crosswalk to 86833
Gapfill
Abstain"	"10 out of 11
0 out of 11
1 out of 11"				
133	0584U	"Neurology (prion disease), cerebrospinal fluid, detection of prion protein by quakinginduced conformational conversion, qualitative"	"Crosswalk to 0035U
Gapfill
Abstain"	"10 out of 11
0 out of 11
1 out of 11"				
134	0585U	"Targeted genomic sequence analysis panel, solid organ neoplasm, circulating cell-free dna (cfdna) analysis from plasma of 521 genes, interrogation for sequence variants, gene copy number amplifications, gene rearrangements, and microsatellite instability, report shows identified mutations, including variants with clinical actionability"	"Crosswalk to 81455
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
135	0586U	"Oncology, mrna, gene expression profiling of 216 genes (204 targeted and 12 housekeeping genes), rna expression analysis, formalinfixed paraffin-embedded (ffpe) tissue, quantitative, reported as log2 ratio per gene"	"Crosswalk to 81456
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
136	0588U	"Infectious disease (bacterial or viral), 32 genes (29 informative and 3 housekeeping), immune response mrna, gene expression profiling by splitwell multiplex reverse transcription loop-mediated isothermal amplification (rtlamp), whole blood, reported as continuous risk scores for likelihood of bacterial and viral infection and likelihood of severe illness within the next 7 days"	"Crosswalk to 0005U
Crosswalk to 0588U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11
0 out of 11"				
137	0589U	"Perfluoroalkyl substances (pfas) (eg, perfluorooctanoic acid, perfluorooctane sulfonic acid), 24 pfas compounds by high-performance liquid chromatography with tandem mass spectrometry (lcms/ms), plasma or serum, quantitative"	"Crosswalk to 0457U x 1.15
Crosswalk to 0035U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11
0 out of 11"				
138	0591U	"Oncology (prostate cancer), biochemical analysis of 3 proteins (total psa, free psa, and he4), plasma, serum, prognostic algorithm incorporating 3 proteins and digital rectal examination, results reported as a probability score for clinically significant prostate cancer"	"Crosswalk to 81539
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
139	0592U	"Oncology (hematolymphoid neoplasms), dna, targeted genomic sequence of 417 genes, interrogation for gene fusions, translocations, rearrangements, utilizing formalin-fixed paraffinembedded (ffpe) tumor tissue, results report clinically significant variant(s)"	"Crosswalk to 81455
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
140	0593U	"Infectious disease (genitourinary pathogens), dna, 46 targets (28 pathogens, 18 resistance genes), rt-pcr amplified probe technique, urine, each analyte reported as detected or not detected"	"Crosswalk to 87632+ 87633
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
141	0595U	"Infectious disease (tropical fever pathogens), vectorborne and zoonotic pathogens, including 2 viruses (chikungunya virus and dengue virus serotypes 1, 2, 3, and 4), 1 bacterium (leptospira species), and 1 parasite with species differentiation (plasmodium species, plasmodium falciparum, and plasmodium vivax/ovale), real-time rtpcr, whole blood, each pathogen reported as detected or not detected"	"Crosswalk to 87506
Crosswalk to 0595U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11
0 out of 11"				
142	0599U	"Oncology (pancreatic cancer), multiplex immunoassay of icam1, timp1, ctsd, thbs1, and ca 19-9, serum, diagnostic algorithm reported as positive or negative"	"Crosswalk to 81503
Crosswalk to 0599U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11
0 out of 11"				
143	81172	"Aff2 (alf transcription elongation factor 2 [fmr2]) (eg, fragile x intellectual disability 2 [fraxe]) gene analysis; characterization of alleles (eg, expanded size and methylation status)"	"Crosswalk to 81404
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
144	81190	"Cstb (cystatin b) (eg, unverricht-lundborg disease) gene analysis; known familial variant(s)"	"Crosswalk to 81403
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
145	81274	"Htt (huntingtin) (eg, huntington disease) gene analysis; characterization of alleles (eg, expanded size)"	"Crosswalk to 81404
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
146	81289	"Fxn (frataxin) (eg, friedreich ataxia) gene analysis; known familial variant(s)"	"Crosswalk to 81403
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
147	81337	"Smn1 (survival of motor neuron 1, telomeric) (eg, spinal muscular atrophy) gene analysis; known familial sequence variant(s)"	"Crosswalk to 81403
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
148	81349	"Cytogenomic (genome-wide) analysis for constitutional chromosomal abnormalities; interrogation of genomic regions for copy number and loss-of-heterozygosity variants, low-pass sequencing analysis"	"Crosswalk to 81229
Crosswalk to 81349
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11
0 out of 11"				
149	81523	"Oncology (breast), mrna, next-generation sequencing gene expression profiling of 70 content genes and 31 housekeeping genes, utilizing formalin-fixed paraffin-embedded tissue, algorithm reported as index related to risk to distant metastasis"	"Crosswalk to 81523
Crosswalk to 81521
Gapfill
Abstain"	"0 out of 11
10 out of 11
0 out of 11
1 out of 11"				
150	87494	Chlmy trch&neisra gonor mult	"Crosswalk to 87491+ 87591
Crosswalk to 87494
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11
0 out of 11"				
151	87812	Sarscov2&inf typ a&b w/optic	"Crosswalk to 87811+ 87804 x 2
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
152	P2028	"Cephalin floculation, blood"	"Crosswalk to 82040
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
153	P2029	"Congo red, blood"	"Crosswalk to 85044
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
154	P2033	"Thymol turbidity, blood"	"Crosswalk to 82040
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
155	P2038	"Mucoprotein, blood (seromucoid) (medical necessity procedure)"	"Crosswalk to 82040
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
156	Q0115	"Post-coital direct, qualitative examinations of vaginal or cervical mucous"	"Crosswalk to 89300
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
157	0018M	"Transplantation medicine (allograft rejection, renal), measurement of donor and third-party-induced cd154+t-cytotoxic memory cells, utilizing whole peripheral blood, algorithm reported as a rejection risk score"	"Crosswalk to 81595+0540U+0493U+81558
Gapfill
Abstain"	"0 out of 11
11 out of 11
0 out of 11"				
158	0019U	"Oncology, rna, gene expression by whole transcriptome sequencing, formalin-fixed paraffin embedded tissue or fresh frozen tissue, predictive algorithm reported as potential targets for therapeutic agents"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
159	0021U	"Oncology (prostate), detection of 8 autoantibodies (arf 6, nkx3-1, 5'-utr-bmi1, cep 164, 3'-utr-ropporin, desmocollin, aurkaip-1, csnk2a2), multiplexed immunoassay and flow cytometry serum, algorithm reported as risk score"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
160	0022U	"Targeted genomic sequence analysis panel, non-small cell lung neoplasia, dna and rna analysis, 23 genes, interrogation for sequence variants and rearrangements, reported as presence or absence of variants and associated therapy(ies) to consider"	"Crosswalk to 0543 x 0.65
Gapfill
Abstain"	"0 out of 11
10 out of 11
1 out of 11"				
161	0055U	"Cardiology (heart transplant), cell-free dna, pcr assay of 96 dna target sequences (94 single nucleotide polymorphism targets and two control targets), plasma"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
162	0062U	"Autoimmune (systemic lupus erythematosus), igg and igm analysis of 80 biomarkers, utilizing serum, algorithm reported with a risk score"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
163	0083U	"Oncology, response to chemotherapy drugs using motility contrast tomography, fresh or frozen tissue, reported as likelihood of sensitivity or resistance to drugs or drug combinations"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
164	0102U	"Hereditary breast cancer-related disorders (eg, hereditary breast cancer, hereditary ovarian cancer, hereditary endometrial cancer), genomic sequence analysis panel utilizing a combination of ngs, sanger, mlpa, and array cgh, with mmrna analytics to resolve variants of unknown significance when indicated (17 genes [sequencing and deletion/duplication])"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
165	0103U	"Hereditary ovarian cancer (eg, hereditary ovarian cancer, hereditary endometrial cancer), genomic sequence analysis panel utilizing a combination of ngs, sanger, mlpa, and array cgh, with mmrna analytics to resolve variants of unknown significance when indicated (24 genes [sequencing and deletion/duplication], epcam [deletion/duplication only])"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
166	0114U	"Gastroenterology (barrett's esophagus), vim and ccna1 methylation analysis, esophageal cells, algorithm reported as likelihood for barrett's esophagus"	"Crosswalk to 0114U
Gapfill
Abstain"	"0 out of 11
10 out of 11
1 out of 11"				
167	0121U	"Sickle cell disease, microfluidic flow adhesion (vcam-1), whole blood"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
168	0122U	"Sickle cell disease, microfluidic flow adhesion (p-selectin), whole blood"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
169	0123U	"Mechanical fragility, rbc, shear stress and spectral analysis profiling"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
170	0133U	"Hereditary prostate cancer-related disorders, targeted mrna sequence analysis panel (11 genes) (list separately in addition to code for primary procedure)"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
171	0136U	"Atm (ataxia telangiectasia mutated) (eg, ataxia telangiectasia) mrna sequence analysis (list separately in addition to code for primary procedure)"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
172	0137U	"Palb2 (partner and localizer of brca2) (eg, breast and pancreatic cancer) mrna sequence analysis (list separately in addition to code for primary procedure)"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
173	0153U	"Oncology (breast), mrna, gene expression profiling by next-generation sequencing of 101 genes, utilizing formalin-fixed paraffin-embedded tissue, algorithm reported as a triple negative breast cancer clinical subtype(s) with information on immune cell involvement"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
174	0156U	"Copy number (eg, intellectual disability, dysmorphology), sequence analysis"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
175	0157U	"Apc (apc regulator of wnt signaling pathway) (eg, familial adenomatosis polyposis [fap]) mrna sequence analysis (list separately in addition to code for primary procedure)"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
176	0158U	"Mlh1 (mutl homolog 1) (eg, hereditary non-polyposis colorectal cancer, lynch syndrome) mrna sequence analysis (list separately in addition to code for primary procedure)"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
177	0159U	"Msh2 (muts homolog 2) (eg, hereditary colon cancer, lynch syndrome) mrna sequence analysis (list separately in addition to code for primary procedure)"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
178	0160U	"Msh6 (muts homolog 6) (eg, hereditary colon cancer, lynch syndrome) mrna sequence analysis (list separately in addition to code for primary procedure)"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
179	0161U	"Pms2 (pms1 homolog 2, mismatch repair system component) (eg, hereditary nonpolyposis colorectal cancer, lynch syndrome) mrna sequence analysis (list separately in addition to code for primary procedure)"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
180	0162U	"Hereditary colon cancer (lynch syndrome), targeted mrna sequence analysis panel (mlh1, msh2, msh6, pms2) (list separately in addition to code for primary procedure)"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
181	0164U	"Gastroenterology (irritable bowel syndrome [ibs]), immunoassay for anti-cdtb and anti-vinculin antibodies, utilizing plasma, algorithm for elevated or not elevated qualitative results"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
182	0165U	"Peanut allergen-specific quantitative assessment of multiple epitopes using enzyme-linked immunosorbent assay (elisa), blood, individual epitope results and probability of peanut allergy"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
183	0171U	"Targeted genomic sequence analysis panel, acute myeloid leukemia, myelodysplastic syndrome, and myeloproliferative neoplasms, dna analysis, 23 genes, interrogation for sequence variants, rearrangements and minimal residual disease, reported as presence/absence"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
184	0178U	"Peanut allergen-specific quantitative assessment of multiple epitopes using enzyme-linked immunosorbent assay (elisa), blood, report of minimum eliciting exposure for a clinical reaction"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
185	0179U	"Oncology (non-small cell lung cancer), cell-free dna, targeted sequence analysis of 23 genes (single nucleotide variations, insertions and deletions, fusions without prior knowledge of partner/breakpoint, copy number variations), with report of significant mutation(s)"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
186	0212U	"Rare diseases (constitutional/heritable disorders), whole genome and mitochondrial dna sequence analysis, including small sequence changes, deletions, duplications, short tandem repeat gene expansions, and variants in non-uniquely mappable regions, blood or saliva, identification and categorization of genetic variants, proband"	"Crosswalk to 0212U
Gapfill
Abstain"	"0 out of 11
11 out of 11
0 out of 11"				
187	0213U	"Rare diseases (constitutional/heritable disorders), whole genome and mitochondrial dna sequence analysis, including small sequence changes, deletions, duplications, short tandem repeat gene expansions, and variants in non-uniquely mappable regions, blood or saliva, identification and categorization of genetic variants, each comparator genome (eg, parent, sibling)"	"Crosswalk to 0213U
Gapfill
Abstain"	"0 out of 11
11 out of 11
0 out of 11"				
188	0214U	"Rare diseases (constitutional/heritable disorders), whole exome and mitochondrial dna sequence analysis, including small sequence changes, deletions, duplications, short tandem repeat gene expansions, and variants in non-uniquely mappable regions, blood or saliva, identification and categorization of genetic variants, proband"	"Crosswalk to 0214U
Gapfill
Abstain"	"0 out of 11
11 out of 11
0 out of 11"				
189	0215U	"Rare diseases (constitutional/heritable disorders), whole exome and mitochondrial dna sequence analysis, including small sequence changes, deletions, duplications, short tandem repeat gene expansions, and variants in non-uniquely mappable regions, blood or saliva, identification and categorization of genetic variants, each comparator exome (eg, parent, sibling)"	"Crosswalk to 0215U
Gapfill
Abstain"	"0 out of 11
11 out of 11
0 out of 11"				
190	0216U	"Neurology (inherited ataxias), genomic dna sequence analysis of 12 common genes including small sequence changes, deletions, duplications, short tandem repeat gene expansions, and variants in non-uniquely mappable regions, blood or saliva, identification and categorization of genetic variants"	"Crosswalk to 0216U
Gapfill
Abstain"	"0 out of 11
11 out of 11
0 out of 11"				
191	0217U	"Neurology (inherited ataxias), genomic dna sequence analysis of 51 genes including small sequence changes, deletions, duplications, short tandem repeat gene expansions, and variants in non-uniquely mappable regions, blood or saliva, identification and categorization of genetic variants"	"Crosswalk to 0217U
Gapfill
Abstain"	"0 out of 11
11 out of 11
0 out of 11"				
192	0222U	"Red cell antigen (rh blood group) genotyping (rhd and rhce), gene analysis, next-generation sequencing, rh proximal promoter, exons 1-10, portions of introns 2-3"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
193	0226U	"Surrogate viral neutralization test (svnt), severe acute respiratory syndrome coronavirus 2 (sars-cov-2) (coronavirus disease [covid-19]), elisa, plasma, serum"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
194	0228U	"Oncology (prostate), multianalyte molecular profile by photometric detection of macromolecules adsorbed on nanosponge array slides with machine learning, utilizing first morning voided urine, algorithm reported as likelihood of prostate cancer"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
195	0245U	"Oncology (thyroid), mutation analysis of 10 genes and 37 rna fusions and expression of 4 mrna markers using next-generation sequencing, fine needle aspirate, report includes associated risk of malignancy expressed as a percentage"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
196	0248U	"Oncology, spheroid cell culture in 3d microenvironment, 12-drug panel, brain- or brain metastasis- response prediction for each drug"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
197	0253U	"Reproductive medicine (endometrial receptivity analysis), rna gene expression profile, 238 genes by next-generation sequencing, endometrial tissue, predictive algorithm reported as endometrial window of implantation (eg, pre-receptive, receptive, post-receptive)"	"Crosswalk to 0253U
Gapfill
Abstain"	"0 out of 11
11 out of 11
0 out of 11"				
198	0254U	"Reproductive medicine (preimplantation genetic assessment), analysis of 24 chromosomes using embryonic dna genomic sequence analysis for aneuploidy, and a mitochondrial dna score in euploid embryos, results reported as normal (euploidy), monosomy, trisomy, or partial deletion/duplications, mosaicism, and segmental aneuploidy, per embryo tested"	"Crosswalk to 0254U
Gapfill
Abstain"	"0 out of 11
11 out of 11
0 out of 11"				
199	0255U	"Andrology (infertility), sperm-capacitation assessment of ganglioside gm1 distribution patterns, fluorescence microscopy, fresh or frozen specimen, reported as percentage of capacitated sperm and probability of generating a pregnancy score"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
200	0262U	"Oncology (solid tumor), gene expression profiling by real-time rt-pcr of 7 gene pathways (er, ar, pi3k, mapk, hh, tgfb, notch), formalin-fixed paraffinembedded (ffpe), algorithm reported as gene pathway activity score"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
201	0265U	"Rare constitutional and other heritable disorders, whole genome and mitochondrial dna sequence analysis, blood, frozen and formalin-fixed paraffinembedded (ffpe) tissue, saliva, buccal swabs or cell lines, identification of single nucleotide and copy number variants"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
202	0266U	"Unexplained constitutional or other heritable disorders or syndromes, tissuespecific gene expression by wholetranscriptome and next-generation sequencing, blood, formalin-fixed paraffinembedded (ffpe) tissue or fresh frozen tissue, reported as presence or absence of splicing or expression changes"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
203	0268U	"Hematology (atypical hemolytic uremic syndrome [ahus]), genomic sequence analysis of 15 genes, blood, buccal swab, or amniotic fluid"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
204	0269U	"Hematology (autosomal dominant congenital thrombocytopenia), genomic sequence analysis of 22 genes, blood, buccal swab, or amniotic fluid"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
205	0270U	"Hematology (congenital coagulation disorders), genomic sequence analysis of 20 genes, blood, buccal swab, or amniotic fluid"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
206	0271U	"Hematology (congenital neutropenia), genomic sequence analysis of 24 genes, blood, buccal swab, or amniotic fluid"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
207	0272U	"Hematology (genetic bleeding disorders), genomic sequence analysis of 60 genes and duplication/deletion of plau, blood, buccal swab, or amniotic fluid, comprehensive"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
208	0273U	"Hematology (genetic hyperfibrinolysis, delayed bleeding), genomic sequence analysis of 8 genes (f13a1, f13b, fga, fgb, fgg, serpina1, serpine1, serpinf2, plau), blood, buccal swab, or amniotic fluid"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
209	0274U	"Hematology (genetic platelet disorders), genomic sequence analysis of 62 genes and duplication/deletion of plau, blood, buccal swab, or amniotic fluid"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
210	0277U	"Hematology (genetic platelet function disorder), genomic sequence analysis of 40 genes and duplication/deletion of plau, blood, buccal swab, or amniotic fluid"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
211	0285U	"Oncology, disease progression and response monitoring to radiation, chemotherapy, or other systematic cancer treatments, cell-free dna, quantitative branched chain dna amplification, plasma, reported in ng/ml"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
212	0291U	"Psychiatry (mood disorders), mrna, gene expression profiling by rna sequencing 144 genes, whole blood, algorithm reported as predictive risk score"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
213	0292U	"Psychiatry (stress disorders), mrna, gene expression profiling by rna sequencing of 72 genes, whole blood, algorithm reported as predictive risk score"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
214	0297U	"Oncology (pan tumor), whole genome sequencing of paired malignant and normal dna specimens, fresh or formalin-fixed paraffin-embedded (ffpe) tissue, blood or bone marrow, comparative sequence analyses and variant identification"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
215	0301U	"Infectious agent detection by nucleic acid (dna or rna), bartonella henselae and bartonella quintana, droplet digital pcr (ddpcr)"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
216	0302U	"Infectious agent detection by nucleic acid (dna or rna), bartonella henselae and bartonella quintana, droplet digital pcr (ddpcr); following liquid enrichment"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
217	0303U	"Hematology, red blood cell (rbc) adhesion to endothelial/subendothelial adhesion molecules, functional assessment, whole blood, with algorithmic analysis and result reported as an rbc adhesion index; hypoxic"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
218	0304U	"Hematology, red blood cell (rbc) adhesion to endothelial/subendothelial adhesion molecules, functional assessment, whole blood, with algorithmic analysis and result reported as an rbc adhesion index; normoxic"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
219	0305U	"Hematology, red blood cell (rbc) functionality and deformity as a function of shear stress, whole blood, reported as a maximum elongation index"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
220	0306U	"Oncology (minimal residual disease [mrd]), next-generation targeted sequencing analysis, cell-free dna, initial (baseline) assessment to determine a patient-specific panel for future comparisons to evaluate for mrd"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
221	0307U	"Oncology (minimal residual disease [mrd]), next-generation targeted sequencing analysis of a patient-specific panel, cell-free dna, subsequent assessment with comparison to previously analyzed patient specimens to evaluate for mrd"	"Crosswalk to 0569U
Crosswalk to 0467U
Gapfill
Abstain"	"0 out of 11
0 out of 11
11 out of 11
0 out of 11"				
222	0314U	"Oncology (cutaneous melanoma), mrna gene expression profiling by rt-pcr of 35 genes (32 content and 3 housekeeping), utilizing formalin-fixed paraffin-embedded (ffpe) tissue, algorithm reported as a categorical result (ie, benign, intermediate, malignant)"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
223	0333U	"Oncology (liver), surveillance for hepatocellular carcinoma (hcc) in highrisk patients, analysis of methylation patterns on circulating cell-free dna (cfdna) plus measurement of serum of afp/afp-l3 and oncoprotein des-gammacarboxy-prothrombin (dcp), algorithm reported as normal or abnormal result"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
224	0341U	"Fetal aneuploidy dna sequencing comparative analysis, fetal dna from products of conception, reported as normal (euploidy), monosomy, trisomy, or partial deletion/duplication, mosaicism, and segmental aneuploid"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
225	0368U	"Oncology (colorectal cancer), evaluation for mutations of apc, braf, ctnnb1, kras, nras, pik3ca, smad4, and tp53, and methylation markers (myo1g, kcnq5, c9orf50, fli1, clip4, znf132 and twist1), multiplex quantitative polymerase chain reaction (qpcr), circulating cell-free dna (cfdna), plasma, report of risk score for advanced adenoma or colorectal cancer"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
226	0381U	"Maple syrup urine disease monitoring by patient-collected blood card sample, quantitative measurement of allo-isoleucine, leucine, isoleucine, and valine, liquid chromatography with tandem mass spectrometry (lc-ms/ms)"	"Crosswalk to 0381U
Gapfill
Abstain"	"0 out of 11
11 out of 11
0 out of 11"				
227	0383U	"Tyrosinemia type i monitoring by patient-collected blood card sample, quantitative measurement of tyrosine, phenylalanine, methionine, succinylacetone, nitisinone, liquid chromatography with tandem mass spectrometry (lc-ms/ms)"	"Crosswalk to 0383U
Gapfill
Abstain"	"0 out of 11
11 out of 11
0 out of 11"				
228	0389U	"Pediatric febrile illness (kawasaki disease [kd]), interferon alphainducible protein 27 (ifi27) and mast cell-expressed membrane protein 1 (mcemp1), rna, using reverse transcription polymerase chain reaction (rt-qpcr), blood, reported as a risk score for kd"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
229	0395U	"Oncology (lung), multi-omics (microbial dna by shotgun nextgeneration sequencing and carcinoembryonic antigen and osteopontin by immunoassay), plasma, algorithm reported as malignancy risk for lung nodules in early-stage disease"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
230	0399U	"Neurology (cerebral folate deficiency), serum, detection of anti-human folate receptor iggbinding antibody and blocking autoantibodies by enzyme-linked immunoassay (elisa), qualitative, and blocking autoantibodies, using a functional blocking assay for igg or igm, quantitative, reported as positive or not detected"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
231	0400U	"Obstetrics (expanded carrier screening), 145 genes by nextgeneration sequencing, fragment analysis and multiplex ligationdependent probe amplification, dna, reported as carrier positive or negative"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
232	0401U	"Cardiology (coronary heart disease [cad]), 9 genes (12 variants), targeted variant genotyping, blood, saliva, or buccal swab, algorithm reported as a genetic risk score for a coronary event"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
233	0408U	"Infectious agent antigen detection by bulk acoustic wave biosensor immunoassay, severe acute respiratory syndrome coronavirus 2 (sars-cov-2) (coronavirus disease [covid-19])"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
234	0417U	"Rare diseases (constitutional/heritable disorders), whole mitochondrial genome sequence with heteroplasmy detection and deletion analysis, nuclear-encoded mitochondrial gene analysis of 335 nuclear genes, including sequence changes, deletions, insertions, and copy number variants analysis, blood or saliva, identification and categorization of mitochondrial disorder-associated genetic variants"	"Crosswalk to 0417U
Gapfill
Abstain"	"0 out of 11
11 out of 11
0 out of 11"				
235	0436U	"Oncology (lung), plasma analysis of 388 proteins, using aptamer-based proteomics technology, predictive algorithm reported as clinical benefit from immune checkpoint inhibitor therapy"	"Crosswalk to 0436U
Gapfill
Abstain"	"0 out of 11
11 out of 11
0 out of 11"				
236	0439U	"Cardiology (coronary heart disease [chd]), dna, analysis of 5 single-nucleotide polymorphisms (snps) (rs11716050 [loc105376934], rs6560711 [wdr37], rs3735222 [scin/loc107986769], rs6820447 [intergenic], and rs9638144 [esyt2]) and 3 dna methylation markers (cg00300879 [transcription start site {tss200} of cnksr1], cg09552548 [intergenic], and cg14789911 [body of spatc1l]), qpcr and digital pcr, whole blood, algorithm reported as a 4-tiered risk score for a 3-year risk of symptomatic chd"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
237	0440U	"Cardiology (coronary heart disease [chd]), dna, analysis of 10 single-nucleotide polymorphisms (snps) (rs710987 [linc010019], rs1333048 [cdkn2b-as1], rs12129789 [kcnd3], rs942317 [ktn1-as1], rs1441433 [ppp3ca], rs2869675 [prex1], rs4639796 [zbtb41], rs4376434 [linc00972], rs12714414 [tmem18], and rs7585056 [tmem18]) and 6 dna methylation markers (cg03725309 [sars1], cg12586707 [cxcl1, cg04988978 [mpo], cg17901584 [dhcr24-dt], cg21161138 [ahrr], and cg12655112 [ehd4]), qpcr and digital pcr, whole blood, algorithm reported as detected or not detected for chd"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
238	0441U	"Infectious disease (bacterial, fungal, or viral infection), semiquantitative biomechanical assessment (via deformability cytometry), whole blood, with algorithmic analysis and result reported as an index"	"Crosswalk to 0441U
Crosswalk to 0312U x .55
Gapfill
Abstain"	"0 out of 11
0 out of 11
10 out of 11
1 out of 11"				
239	0463U	"Oncology (cervix), mrna gene expression profiling of 14 biomarkers (e6 and e7 of the highest-risk human papillomavirus [hpv] types 16, 18, 31, 33, 45, 52, 58), by real-time nucleic acid sequence-based amplification (nasba), exo- or endocervical epithelial cells, algorithm reported as positive or negative for increased risk of cervical dysplasia or cancer for each biomarker"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
240	0466U	"Cardiology (coronary artery disease [cad]), dna, genomewide association studies (564856 single-nucleotide polymorphisms [snps], targeted variant genotyping), patient lifestyle and clinical data, buccal swab, algorithm reported as polygenic risk to acquired heart disease"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
241	0470U	"Oncology (oropharyngeal), detection of minimal residual disease by next-generation sequencing (ngs) based quantitative evaluation of 8 dna targets, cell-free hpv 16 and 18 dna from plasma"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
242	0478U	"Oncology (non-small cell lung cancer), dna and rna, digital pcr analysis of 9 genes (egfr, kras, braf, alk, ros1, ret, ntrk 1/2/3, erbb2, and met) in formalin-fixed paraffin-embedded (ffpe) tissue, interrogation for single-nucleotide variants, insertions/deletions, gene rearrangements, and reported as actionable detected variants for therapy selection"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
243	0483U	"Infectious disease (neisseria gonorrhoeae), sensitivity, ciprofloxacin resistance (gyra s91f point mutation), oral, rectal, or vaginal swab, algorithm reported as probability of fluoroquinolone resistance"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
244	0484U	"Infectious disease (mycoplasma genitalium), macrolide sensitivity (23s rrna point mutation), oral, rectal, or vaginal swab, algorithm reported as probability of macrolide resistance"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
245	0496U	"Oncology (colorectal), cell-free dna, 8 genes for mutations, 7 genes for methylation by real-time rt-pcr, and 4 proteins by enzyme-linked immunosorbent assay, blood, reported positive or negative for colorectal cancer or advanced adenoma risk"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
246	0498U	"Oncology (colorectal), nextgeneration sequencing for mutation detection in 43 genes and methylation pattern in 45 genes, blood, and formalin-fixed paraffin-embedded (ffpe) tissue, report of variants and methylation pattern with interpretation"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
247	0501U	"Oncology (colorectal), blood, quantitative measurement of cellfree dna (cfdna)"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
248	0526U	"Nephrology (renal transplant), quantification of cxcl10 chemokines, flow cytometry, urine, reported as pg/ml creatinine baseline and monitoring over time"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
249	0529U	"Hematology (venous thromboembolism [vte]), genome-wide single-nucleotide polymorphism variants, including f2 and f5 gene analysis, and leiden variant, by microarray analysis, saliva, report as risk score for vte"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
250	0531U	"Infectious disease (acid-fast bacteria and invasive fungi), dna (673 organisms), nextgeneration sequencing, plasm"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
251	0534U	"Oncology (prostate), microrna, single-nucleotide polymorphisms (snps) analysis by rt-pcr of 32 variants, using buccal swab algorithm reported as a risk score"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
252	0542U	"Nephrology (renal transplant), urine, nuclear magnetic resonance (nmr) spectroscopy measurement of 84 urinary metabolites, combined with patient data, quantification of bk virus (human polyomavirus 1) using real-time pcr and serum creatinine, algorithm reported as a probability score for allograft injury status"	"Crosswalk to 0542U
Gapfill
Abstain"	"0 out of 11
11 out of 11
0 out of 11"				
253	0552U	"Reproductive medicine (preimplantation genetic assessment), analysis for known genetic disorders from trophectoderm biopsy, linkage analysis of disease-causing locus, and when possible, targeted mutation analysis for known familial variant, reported as low-risk or high-risk for familial genetic disorder"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
254	0569U	"Oncology (solid tumor), next-generation sequencing analysis of tumor methylation markers (>20000 differentially methylated regions) present in cell-free circulating tumor dna (ctdna), whole blood, algorithm reported as presence or absence of ctdna with tumor fraction, if appropriate"	"Crosswalk to 0569U
Gapfill
Abstain"	"0 out of 11
11 out of 11
0 out of 11"				
255	0572U	"Oncology (prostate), high-throughput telomere length quantification by fish, whole blood, diagnostic algorithm reported as risk of prostate cancer"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
256	0574U	"Mycobacterium tuberculosis, culture filtrate protein?10-kda (cfp-10), serum or plasma, liquid chromatography mass spectrometry (lc-ms)"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
257	0590U	"Infectious disease (bacterial and fungal), dna of 44 organisms (34 bacteria, 10 fungi), urine, next-generation sequencing, reported as positive or negative for each organism"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
258	0594U	"Infectious disease (sepsis), semiquantitative measurement of pancreatic stone protein concentration, whole blood, reported as risk of sepsis"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
259	0597U	"Oncology (breast), rna expression profiling of 329 genes by targeted nextgeneration sequencing and 20 proteins by multiplex immunofluorescence, formalin-fixed paraffinembedded (ffpe) tissue, algorithmic analyses to determine tumor-recurrence risk score"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
260	81493	"Coronary artery disease, mrna, gene expression profiling by real-time rt-pcr of 23 genes, utilizing whole peripheral blood, algorithm reported as a risk score"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
261	81524	"Onc cns tum dna mthyl 10,000"	"Gapfill
Abstain"	"10 out of 11
1 out of 11"				
262	81560	"Transplantation medicine (allograft rejection, pediatric liver and small bowel), measurement of donor and third-party-induced cd154+t-cytotoxic memory cells, utilizing whole peripheral blood, algorithm reported as a rejection risk score"	"Crosswalk to 81959+0540U+0493U+81558
Gapfill
Abstain"	"0 out of 11
11 out of 11
0 out of 11"				
263	87182	Sc std carbapenemase nzm det	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
264	0004M	"Scoliosis, dna analysis of 53 single nucleotide polymorphisms (snps), using saliva, prognostic algorithm reported as a risk score"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
265	0007M	"Oncology (gastrointestinal neuroendocrine tumors), real-time pcr expression analysis of 51 genes, utilizing whole peripheral blood, algorithm reported as a nomogram of tumor disease index"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
266	0082U	"Drug test(s), definitive, 90 or more drugs or substances, definitive chromatography with mass spectrometry, and presumptive, any number of drug classes, by instrument chemistry analyzer (utilizing immunoassay), urine, report of presence or absence of each drug, drug metabolite or substance with description and severity of significant interactions per date of service"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
267	0116U	"Prescription drug monitoring, enzyme immunoassay of 35 or more drugs confirmed with lc-ms/ms, oral fluid, algorithm results reported as a patientcompliance measurement with risk of drug to drug interactions for prescribed medications"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
268	0170U	"Neurology (autism spectrum disorder [asd]), rna, next-generation sequencing, saliva, algorithmic analysis, and results reported as predictive probability of asd diagnosis"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
269	0258U	"Autoimmune (psoriasis), mrna, nextgeneration sequencing, gene expression profiling of 50-100 genes, skin-surface collection using adhesive patch, algorithm reported as likelihood of response to psoriasis biologics"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
270	0260U	"Rare diseases (constitutional/heritable disorders), identification of copy number variations, inversions, insertions, translocations, and other structural variants by optical genome mapping"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
271	0264U	"Rare diseases (constitutional/heritable disorders), identification of copy number variations, inversions, insertions, translocations, and other structural variants by optical genome mapping"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
272	0267U	"Rare constitutional and other heritable disorders, identification of copy number variations, inversions, insertions, translocations, and other structural variants by optical genome mapping and whole genome sequencing"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
273	0296U	"Oncology (oral and/or oropharyngeal cancer), gene expression profiling by rna sequencing of at least 20 molecular features (eg, human and/or microbial mrna), saliva, algorithm reported as positive or negative for signature associated with malignancy"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
274	0299U	"Oncology (pan tumor), whole genome optical genome mapping of paired malignant and normal dna specimens, fresh frozen tissue, blood, or bone marrow, comparative structural variant identification"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
275	0300U	"Oncology (pan tumor), whole genome sequencing and optical genome mapping of paired malignant and normal dna specimens, fresh tissue, blood, or bone marrow, comparative sequence analyses and variant identification"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
276	0317U	"Oncology (lung cancer), four-probe fish (3q29, 3p22.1, 10q22.3, 10cen) assay, whole blood, predictive algorithm-generated evaluation reported as decreased or increased risk for lung cancer"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
277	0328U	"Drug assay, definitive, 120 or more drugs and metabolites, urine, quantitative liquid chromatography with tandem mass spectrometry (lc-ms/ms), includes specimen validity and algorithmic analysis describing drug or metabolite and presence or absence of risks for a significant patient-adverse event, per date of service"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
278	0331U	"Oncology (hematolymphoid neoplasia), optical genome mapping for copy number alterations and gene rearrangements utilizing dna from blood or bone marrow, report of clinically significant alterations"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
279	0335U	"Rare diseases (constitutional/heritable disorders), whole genome sequence analysis, including small sequence changes, copy number variants, deletions, duplications, mobile element insertions, uniparental disomy (upd), inversions, aneuploidy, mitochondrial genome sequence analysis with heteroplasmy and large deletions, short tandem repeat (str) gene expansions, fetal sample, identification and categorization of genetic variants"	"Crosswalk to 0335U
Gapfill
Abstain"	"0 out of 11
11 out of 11
0 out of 11"				
280	0336U	"Rare diseases (constitutional/heritable disorders), whole genome sequence analysis, including small sequence changes, copy number variants, deletions, duplications, mobile element insertions, uniparental disomy (upd), inversions, aneuploidy, mitochondrial genome sequence analysis with heteroplasmy and large deletions, short tandem repeat (str) gene expansions, blood or saliva, identification and categorization of genetic variants, each comparator genome (eg, parent)"	"Crosswalk to 0336U
Gapfill
Abstain"	"0 out of 11
11 out of 11
0 out of 11"				
281	0391U	"Oncology (solid tumor), dna and rna by next-generation sequencing, utilizing formalin-fixed paraffin-embedded (ffpe) tissue, 437 genes, interpretive report for single nucleotide variants, splicesite variants, insertions/deletions, copy number alterations, gene fusions, tumor mutational burden, and microsatellite instability, with algorithm quantifying immunotherapy response score"	"Crosswalk 0026U ** (Update)
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
282	0413U	"Oncology (hematolymphoid neoplasm), optical genome mapping for copy number alterations, aneuploidy, and balanced/complex structural rearrangements, dna from blood or bone marrow, report of clinically significant alterations"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
283	0435U	"Oncology, chemotherapeutic drug cytotoxicity assay of cancer stem cells (cscs), from cultured cscs and primary tumor cells, categorical drug response reported based on cytotoxicity percentage observed, minimum of 14 drugs or drug combinations"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
284	0454U	"Rare diseases (constitutional/heritable disorders), identification of copy number variations, inversions, insertions, translocations, and other structural variants by optical genome mapping"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
285	0465U	"Oncology (urothelial carcinoma), dna, quantitative methylationspecific pcr of 2 genes (onecut2, vim), algorithmic analysis reported as positive or negative"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
286	0467U	"Oncology (bladder), dna, nextgeneration sequencing (ngs) of 60 genes and whole genome aneuploidy, urine, algorithms reported as minimal residual disease (mrd) status positive or negative and quantitative disease burden"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
287	0506U	"Gastroenterology (barrett's esophagus), esophageal cells, dna methylation analysis by next-generation sequencing of at least 89 differentially methylated genomic regions, algorithm reported as likelihood for barrett's esophagus"	"Crosswalk to 0114U
Gapfill
Abstain"	"0 out of 11
11 out of 11
0 out of 11"				
288	0511U	"Oncology (solid tumor), tumor cell culture in 3d microenvironment, 36 or more drug panel, reported as tumor-response prediction for each drug"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
289	0523U	"Oncology (solid tumor), dna, qualitative, next-generation sequencing (ngs) of single-nucleotide variants (snv) and insertion/deletions in 22 genes utilizing formalin-fixed paraffin-embedded tissue, reported as presence or absence of mutation(s), location of mutation(s), nucleotide change, and amino acid change"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
290	0525U	"Oncology, spheroid cell culture, 11-drug panel (carboplatin, docetaxel, doxorubicin, etoposide, gemcitabine, niraparib, olaparib, paclitaxel, rucaparib, topotecan, veliparib) ovarian, fallopian, or peritoneal response prediction for each drug"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
291	0553U	"Reproductive medicine (preimplantation genetic assessment), analysis of 24 chromosomes using dna genomic sequence analysis from embryonic trophectoderm for structural rearrangements, aneuploidy, and a mitochondrial dna score, results reported as normal/balanced (euploidy/balanced), unbalanced structural rearrangement, monosomy, trisomy, segmental aneuploidy, or mosaic, per embryo tested"	"Crosswalk to 0553U
Gapfill
Abstain"	"0 out of 11
11 out of 11
0 out of 11"				
292	0554U	"Reproductive medicine (preimplantation genetic assessment), analysis of 24 chromosomes using dna genomic sequence analysis from trophectoderm biopsy for aneuploidy, ploidy, a mitochondrial dna score, and embryo quality control, results reported as normal (euploidy), monosomy, trisomy, segmental aneuploidy, triploid, haploid, or mosaic, with quality control results reported as contamination detected or inconsistent cohort when applicable, per embryo tested"	"Crosswalk to 0554U
Gapfill
Abstain"	"0 out of 11
11 out of 11
0 out of 11"				
293	0555U	"Reproductive medicine (preimplantation genetic assessment), analysis of 24 chromosomes using dna genomic sequence analysis from embryonic trophectoderm for structural rearrangements, aneuploidy, ploidy, a mitochondrial dna score, and embryo quality control, results reported as normal/balanced (euploidy/balanced), unbalanced structural rearrangement, monosomy, trisomy, segmental aneuploidy, triploid, haploid, or mosaic, with quality control results reported as contamination detected or inconsistent cohort when applicable, per embryo tested"	"Crosswalk to 0555U
Gapfill
Abstain"	"0 out of 11
11 out of 11
0 out of 11"				
294	0560U	"Oncology (minimal residual disease [mrd]), genomic sequence analysis, cell-free dna, whole blood and tumor tissue, baseline assessment for design and construction of a personalized variant panel to evaluate current mrd and for comparison to subsequent mrd assessments"	"Crosswalk to 0306U
Gapfill
Abstain"	"0 out of 11
11 out of 11
0 out of 11"				
295	0561U	"Oncology (minimal residual disease [mrd]), genomic sequence analysis, cell-free dna, whole blood, subsequent assessment with comparison to initial assessment to evaluate for mrd"	"Crosswalk to 0307U
Gapfill
Abstain"	"0 out of 11
11 out of 11
0 out of 11"				
296	0566U	"Oncology (lung), qpcr-based analysis of 13 differentially methylated regions (ccdc181, hoxa7, lrrc8a, marchf11, mir129-2, ncor2, pantr1, prkcb, slc9a3, tbr1_2, trap1, vwc2, znf781), pleural fluid, algorithm reported as a qualitative result"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
297	0567U	"Rare diseases (constitutional/heritable disorders), whole-genome sequence analysis combination of short and long reads, for single-nucleotide variants, insertions/deletions and characterized intronic variants, copy-number variants, duplications/deletions, mobile element insertions, runs of homozygosity, aneuploidy, and inversions, mitochondrial dna sequence and deletions, short tandem repeat genes, methylation status of selected regions, blood, saliva, amniocentesis, chorionic villus sample or tissue, identification and categorization of genetic variants"	"Crosswalk to 0567U
Gapfill
Abstain"	"0 out of 11
11 out of 11
0 out of 11"				
298	0587U	"Therapeutic drug monitoring, 60-150 drugs and metabolites, urine, saliva, quantitative liquid chromatography with tandem mass spectrometry (lcms/ms), specimen validity, and algorithmic analyses for presence or absence of drug or metabolite, risk score predicted for adverse drug effects"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
299	0598U	"Gastroenterology (irritable bowel syndrome), igg antibodies to 18 food items by microarray-based immunoassay, whole blood or serum, report as elevated (positive) or normal (negative) antibody levels"	"Crosswalk to 0598U
Gapfill
Abstain"	"0 out of 11
11 out of 11
0 out of 11"				
300	80190	Procainamide;	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
301	81195	"Cytogenomic (genome-wide) analysis, hematologic malignancy, structural variants and copy number variants, optical genome mapping (ogm)"	"Crosswalk to 0260U
Crosswalk to 0331U
Gapfill
Abstain"	"0 out of 11
0 out of 11
11 out of 11
0 out of 11"				
302	81354	Cytog alys chrml abnor ogm	"Crosswalk to 0260U
Gapfill
Abstain"	"0 out of 11
11 out of 11
0 out of 11"				
303	81504	"Oncology (tissue of origin), microarray gene expression profiling of > 2000 genes, utilizing formalin-fixed paraffin-embedded tissue, algorithm reported as tissue similarity scores"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
304	81535	"Oncology (gynecologic), live tumor cell culture and chemotherapeutic response by dapi stain and morphology, predictive algorithm reported as a drug response score; first single drug or drug combination"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
305	81536	"Oncology (gynecologic), live tumor cell culture and chemotherapeutic response by dapi stain and morphology, predictive algorithm reported as a drug response score; each additional single drug or drug combination (list separately in addition to code for primary procedure)"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
306	82143	Amniotic fluid scan (spectrophotometric)	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
307	82286	Bradykinin	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
308	82387	Cathepsin-d	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
309	82415	Chloramphenicol	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
310	82485	"Chondroitin b sulfate, quantitative"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
311	82965	Glutamate dehydrogenase	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
312	82979	"Glutathione reductase, rbc"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
313	83045	Hgb methemoglobin qual	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
314	83633	"Lactose, urine, qualitative"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
315	83661	Fetal lung maturity assessment; lecithin sphingomyelin (l/s) ratio	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
316	83662	Fetal lung maturity assessment; foam stability test	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
317	83775	Malate dehydrogenase	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
318	83857	Methemalbumin	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
319	83987	Ph; exhaled breath condensate	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
320	84085	"Phosphogluconate, 6-, dehydrogenase, rbc"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
321	84138	Pregnanetriol	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
322	84203	"Protoporphyrin, rbc; screen"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
323	84233	Receptor assay; estrogen	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
324	84234	Receptor assay; progesterone	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
325	84375	"Sugars, chromatographic, tlc or paper chromatography"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
326	84488	"Trypsin; feces, qualitative"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
327	84577	"Urobilinogen, feces, quantitative"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
328	87152	"Culture, typing; identification by pulse field gel typing"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
329	88147	"Cytopathology smears, cervical or vaginal; screening by automated system under physician supervision"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
330	88152	"Cytopathology, slides, cervical or vaginal; with manual screening and computer-assisted rescreening under physician supervision"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
331	88153	"Cytopathology, slides, cervical or vaginal; with manual screening and rescreening under physician supervision"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
332	88166	"Cytopathology, slides, cervical or vaginal (the bethesda system); with manual screening and computer-assisted rescreening under physician supervision"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
333	88167	"Cytopathology, slides, cervical or vaginal (the bethesda system); with manual screening and computer-assisted rescreening using cell selection and review under physician supervision"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
334	88371	"Protein analysis of tissue by western blot, with interpretation and report;"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
335	88372	"Protein analysis of tissue by western blot, with interpretation and report; immunological probe for band identification, each"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
336	89329	Sperm evaluation; hamster penetration test	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
337	G0147	"Screening cytopathology smears, cervical or vaginal, performed by automated system under physician supervision"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
338	G9143	"Warfarin responsiveness testing by genetic technique using any method, any number of specimen(s)"	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
339	P2031	Hair analysis (excluding arsenic)	"Gapfill
Abstain"	"11 out of 11
0 out of 11"				
340	0002U	"Oncology (colorectal), quantitative assessment of three urine metabolites (ascorbic acid, succinic acid and carnitine) by liquid chromatography with tandem mass spectrometry (lc-ms/ms) using multiple reaction monitoring acquisition, algorithm reported as likelihood of adenomatous polyps"	"Crosswalk to 0256U
Gapfill
Abstain
"	"11 out of 11
0 out of 11
0 out of 11"				
341	0003U	"Oncology (ovarian) biochemical assays of five proteins (apolipoprotein a-1, ca 125 ii, follicle stimulating hormone, human epididymis protein 4, transferrin), utilizing serum, algorithm reported as a likelihood score"	"Crosswalk to 81503
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
342	0009U	"Oncology (breast cancer), erbb2 (her2) copy number by fish, tumor cells from formalin fixed paraffin embedded tissue isolated using image-based dielectrophoresis (dep) sorting, reported as erbb2 gene amplified or non-amplified"	"Crosswalk to 88271 x 2
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
343	0019M	"Cardiovascular disease, plasma, analysis of protein biomarkers by aptamer-based microarray and algorithm reported as 4-year likelihood of coronary event in high-risk populations"	"Crosswalk to 0309U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
344	0030U	"Drug metabolism (warfarin drug response), targeted sequence analysis (ie, cyp2c9, cyp4f2, vkorc1, rs12777823)"	"Crosswalk to 81227+ 81355
Gapfill
Abstain"	"10 out of 11
0 out of 11
1 out of 11"				
345	0048U	"Oncology (solid organ neoplasia), dna, targeted sequencing of protein-coding exons of 468 cancer-associated genes, including interrogation for somatic mutations and microsatellite instability, matched with normal specimens, utilizing formalin-fixed paraffin-embedded tumor tissue, report of clinically significant mutation(s)"	"Crosswalk to 81455
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
346	0050U	"Targeted genomic sequence analysis panel, acute myelogenous leukemia, dna analysis, 194 genes, interrogation for sequence variants, copy number variants or rearrangements"	"Crosswalk to 81455
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
347	0063U	"Neurology (autism), 32 amines by lc-ms/ms, using plasma, algorithm reported as metabolic signature associated with autism spectrum disorder"	"Crosswalk to 0344U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
348	0092U	"Oncology (lung), three protein biomarkers, immunoassay using magnetic nanosensor technology, plasma, algorithm reported as risk score for likelihood of malignancy"	"Crosswalk to 0407U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
349	0095U	"Eosinophilic esophagitis, 2 protein biomarkers (eotaxin-3 [ccl26 {c-c motif chemokine ligand 26}] and major basic protein [prg2 {proteoglycan 2, pro eosinophil major basic protein}], enzyme-linked immunosorbent assays (elisa), specimen obtained by esophageal string test device, algorithm reported as probability of active or inactive eosinophilic esophagitis"	"Crosswalk to 81500
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
350	0105U	"Nephrology (chronic kidney disease), multiplex electrochemiluminescent immunoassay (eclia) of tumor necrosis factor receptor 1a, receptor superfamily 2 (tnfr1, tnfr2), and kidney injury molecule-1 (kim-1) combined with longitudinal clinical data, including apol1 genotype if available, and plasma (isolated fresh or frozen), algorithm reported as probability score for rapid kidney function decline (rkfd)"	"Crosswalk to 0308U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
351	0117U	"Pain management, analysis of 11 endogenous analytes (methylmalonic acid, xanthurenic acid, homocysteine, pyroglutamic acid, vanilmandelate, 5hydroxyindoleacetic acid, hydroxymethylglutarate, ethylmalonate, 3hydroxypropyl mercapturic acid (3-hpma), quinolinic acid, kynurenic acid), lcms/ms, urine, algorithm reported as a pain-index score with likelihood of atypical biochemical function associated with pain"	"Crosswalk to 0344U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
352	0163U	"Oncology (colorectal) screening, biochemical enzyme-linked immunosorbent assay (elisa) of 3 plasma or serum proteins (teratocarcinoma derived growth factor-1 [tdgf-1, cripto- 1], carcinoembryonic antigen [cea], extracellular matrix protein [ecm]), with demographic data (age, gender, crc-screening compliance) using a proprietary algorithm and reported as likelihood of crc or advanced adenomas"	"Crosswalk to 0308U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
353	0174U	"Oncology (solid tumor), mass spectrometric 30 protein targets, formalin-fixed paraffin-embedded tissue, prognostic and predictive algorithm reported as likely, unlikely, or uncertain benefit of 39 chemotherapy and targeted therapeutic oncology agents"	"Crosswalk to 0344U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
354	0180U	"Red cell antigen (abo blood group) genotyping (abo), gene analysis sanger/chain termination/conventional sequencing, abo (abo, alpha 1-3-n-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase) gene, including subtyping, 7 exons"	"Crosswalk to 81405
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
355	0221U	"Red cell antigen (abo blood group) genotyping (abo), gene analysis, next-generation sequencing, abo (abo, alpha 1-3-n-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase) gene"	"Crosswalk to 81404
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
356	0244U	"Oncology (solid organ), dna, comprehensive genomic profiling, 257 genes, interrogation for single-nucleotide variants, insertions/deletions, copy number alterations, gene rearrangements, tumor-mutational burden and microsatellite instability, utilizing formalin-fixed paraffin-embedded tumor tissue"	"Crosswalk to 81455
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
357	0247U	"Obstetrics (preterm birth), insulin-like growth factor-binding protein 4 (ibp4), sex hormone-binding globulin (shbg), quantitative measurement by lc-ms/ms, utilizing maternal serum, combined with clinical data, reported as predictive-risk stratification for spontaneous preterm birth"	"Crosswalk to 0256U
Crosswalk to 0247U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11
0 out of 11"				
358	0249U	"Oncology (breast), semiquantitative analysis of 32 phosphoproteins and protein analytes, includes laser capture microdissection, with algorithmic analysis and interpretative report"	"Crosswalk to 0344U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
359	0252U	"Fetal aneuploidy short tandem-repeat comparative analysis, fetal dna from products of conception, reported as normal (euploidy), monosomy, trisomy, or partial deletion/duplications, mosaicism, and segmental aneuploidy"	"Crosswalk to 81265
Crosswalk to 0252U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11
0 out of 11"				
360	0263U	"Neurology (autism spectrum disorder [asd]), quantitative measurements of 16 central carbon metabolites (ie, ketoglutarate, alanine, lactate, phenylalanine, pyruvate, succinate, carnitine, citrate, fumarate, hypoxanthine, inosine, malate, s-sulfocysteine, taurine, urate, and xanthine), liquid chromatography tandem mass spectrometry (lc-ms/ms), plasma, algorithmic analysis with result reported as negative or positive (with metabolic subtypes of asd)"	"Crosswalk to 0344U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
361	0286U	"Cep72 (centrosomal protein, 72-kda), nudt15 (nudix hydrolase 15) and tpmt (thiopurine s-methyltransferase) (eg, drug metabolism) gene analysis, common variants"	"Crosswalk to 81306+ 81335
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
362	0310U	"Pediatrics (vasculitis, kawasaki disease [kd]), analysis of 3 biomarkers (nt-probnp, c-reactive protein, and t-uptake), plasma, algorithm reported as a risk score for kd"	"Crosswalk to 0308U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
363	0319U	"Nephrology (renal transplant), rna expression by select transcriptome sequencing, using pretransplant peripheral blood, algorithm reported as a risk score for early acute rejection"	"Crosswalk to 0320U
Crosswalk to 0319U
Gapfill
Abstain"	"10 out of 11
0 out of 11
0 out of 11
1 out of 11"				
364	0322U	"Neurology (autism spectrum disorder [asd]), quantitative measurements of 14 acyl carnitines and microbiome-derived metabolites, liquid chromatography with tandem mass spectrometry (lc-ms/ms), plasma, results reported as negative or positive for risk of metabolic subtypes associated with asd"	"Crosswalk to 0344U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
365	0384U	"Nephrology (chronic kidney disease), carboxymethyllysine, methylglyoxal hydroimidazolone, and carboxyethyl lysine by liquid chromatography with tandem mass spectrometry (lc-ms/ms) and hba1c and estimated glomerular filtration rate (gfr), with risk score reported for predictive progression to high-stage kidney disease"	"Crosswalk to 0503U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
366	0388U	"Oncology (non-small cell lung cancer), next-generation sequencing with identification of single nucleotide variants, copy number variants, insertions and deletions, and structural variants in 37 cancer-related genes, plasma, with report for alteration detection"	"Crosswalk to 81462
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
367	0573U	"Oncology (pancreas), 3 biomarkers (glucose, carcinoembryonic antigen, and gastricsin), pancreatic cyst lesion fluid, algorithm reported as categorical mucinous or non-mucinous"	"Crosswalk to 81517
Crosswalk to 0573U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11
0 out of 11"				
368	80406	Acth stimulation panel; for 3 beta-hydroxydehydrogenase deficiency this panel must include the following: cortisol (82533 x 2) 17 hydroxypregnenolone (84143 x 2)	"Crosswalk to 82533 x 2+ 84143 x 2
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
369	80410	"Calcitonin stimulation panel (eg, calcium, pentagastrin) this panel must include the following: calcitonin (82308 x 3)"	"Crosswalk to 82308 x 3
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
370	80412	Corticotropic releasing hormone (crh) stimulation panel this panel must include the following: cortisol (82533 x 6) adrenocorticotropic hormone (acth) (82024 x 6)	"Crosswalk to 82533 x 6+ 82024 x 6
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
371	80416	"Renal vein renin stimulation panel (eg, captopril) this panel must include the following: renin (84244 x 6)"	"Crosswalk to 84244 x 6
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
372	80418	Combined rapid anterior pituitary evaluation panel this panel must include the following: adrenocorticotropic hormone (acth) (82024 x 4) luteinizing hormone (lh) (83002 x 4) follicle stimulating hormone (fsh) (83001 x 4) prolactin (84146 x 4) human growth hormone (hgh) (83003 x 4) cortisol (82533 x 4) thyroid stimulating hormone (tsh) (84443 x 4)	"Crosswalk to 82024 x 4+ 83002 x 4+ 83001 x 4+ 84146 x 4+ 83003 x 4+ 82533 x 4+ 84443 x 4
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11
0 out of 11"				
373	80432	Insulin-induced c-peptide suppression panel this panel must include the following: insulin (83525) c-peptide (84681 x 5) glucose (82947 x 5)	"Crosswalk to 83525+ 84681 x 5+ 82947 x 5
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
374	80434	Insulin tolerance panel; for acth insufficiency this panel must include the following: cortisol (82533 x 5) glucose (82947 x 5)	"Crosswalk to 82533 x 5+ 82947 x 5
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
375	81313	"Pca3/klk3 (prostate cancer antigen 3 [non-protein coding]/kallikrein-related peptidase 3 [prostate specific antigen]) ratio (eg, prostate cancer)"	"Crosswalk to 81315
Crosswalk to 81313
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11
0 out of 11"				
376	81341	"Trb@ (t cell antigen receptor, beta) (eg, leukemia and lymphoma), gene rearrangement analysis to detect abnormal clonal population(s); using direct probe methodology (eg, southern blot)"	"Crosswalk to 81262
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
377	81346	"Tyms (thymidylate synthetase) (eg, 5-fluorouracil/5-fu drug metabolism), gene analysis, common variant(s) (eg, tandem repeat variant)"	"Crosswalk to 81227
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
378	81427	"Genome (eg, unexplained constitutional or heritable disorder or syndrome); re-evaluation of previously obtained genome sequence (eg, updated knowledge or unrelated condition/syndrome)"	"Crosswalk to 81427
Crosswalk to 81417
Gapfill
Abstain"	"0 out of 11
10 out of 11
0 out of 11
1 out of 11"				
379	84379	"Sugars (mono-, di-, and oligosaccharides); multiple quantitative, each specimen"	"Crosswalk to 84378 x 2
Crosswalk to 82542
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11
0 out of 11"				
380	84485	Trypsin; duodenal fluid	"Crosswalk to 82977
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
381	85170	Clot retraction	"Crosswalk to 85175 x 0.8
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
382	85337	Thrombomodulin	"Crosswalk to 83520
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
383	85475	"Hemolysin, acid"	"Crosswalk to 86940
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
384	85536	"Iron stain, peripheral blood"	"Crosswalk to 85044
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
385	86155	"Chemotaxis assay, specify method"	"Crosswalk to 86344
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
386	86408	"Neutralizing antibody, severe acute respiratory syndrome coronavirus 2 (sars-cov-2) (coronavirus disease [covid-19]); screen"	"Crosswalk to 86769
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
387	86409	"Neutralizing antibody, severe acute respiratory syndrome coronavirus 2 (sars-cov-2) (coronavirus disease [covid-19]); titer"	"Crosswalk to 86769
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
388	86590	"Streptokinase, antibody"	"Crosswalk to 86406
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
389	86732	Antibody; mucormycosis	"Crosswalk to 86612
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
390	86771	Antibody; shigella	"Crosswalk to 86625
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
391	87003	"Animal inoculation, small animal, with observation and dissection"	"Crosswalk to 87250
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
392	87164	"Dark field examination, any source (eg, penile, vaginal, oral, skin); includes specimen collection"	"Crosswalk to 87166
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
393	87267	"Infectious agent antigen detection by immunofluorescent technique; enterovirus, direct fluorescent antibody (dfa)"	"Crosswalk to 87260
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
394	87271	"Infectious agent antigen detection by immunofluorescent technique; cytomegalovirus, direct fluorescent antibody (dfa)"	"Crosswalk to 87273
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
395	87283	Infectious agent antigen detection by immunofluorescent technique; rubeola	"Crosswalk to 87279
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
396	87320	"Infectious agent antigen detection by immunoassay technique (eg, enzyme immunoassay [eia], enzyme-linked immunosorbent assay [elisa], fluorescence immunoassay [fia], immunochemiluminometric assay [imca]), qualitative or semiquantitative; chlamydia trachomatis"	"Crosswalk to 87808
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
397	87391	"Infectious agent antigen detection by immunoassay technique (eg, enzyme immunoassay [eia], enzyme-linked immunosorbent assay [elisa], fluorescence immunoassay [fia], immunochemiluminometric assay [imca]), qualitative or semiquantitative; hiv-2"	"Crosswalk to 87390
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
398	87472	"Infectious agent detection by nucleic acid (dna or rna); bartonella henselae and bartonella quintana, quantification"	"Crosswalk to 87487
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
399	87475	"Infectious agent detection by nucleic acid (dna or rna); borrelia burgdorferi, direct probe technique"	"Crosswalk to 87540
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
400	87495	"Infectious agent detection by nucleic acid (dna or rna); cytomegalovirus, direct probe technique"	"Crosswalk to 87531
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
401	87525	"Infectious agent detection by nucleic acid (dna or rna); hepatitis g, direct probe technique"	"Crosswalk to 87520
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
402	87526	"Infectious agent detection by nucleic acid (dna or rna); hepatitis g, amplified probe technique"	"Crosswalk to 87521
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
403	87527	"Infectious agent detection by nucleic acid (dna or rna); hepatitis g, quantification"	"Crosswalk to 87522
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
404	87528	Hsv dna dir probe	"Crosswalk to 87531
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
405	87534	"Infectious agent detection by nucleic acid (dna or rna); hiv-1, direct probe technique"	"Crosswalk to 87520
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
406	87537	"Infectious agent detection by nucleic acid (dna or rna); hiv-2, direct probe technique"	"Crosswalk to 87520
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
407	87552	"Infectious agent detection by nucleic acid (dna or rna); mycobacteria species, quantification"	"Crosswalk to 87542
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
408	87557	"Infectious agent detection by nucleic acid (dna or rna); mycobacteria tuberculosis, quantification"	"Crosswalk to 87542
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
409	87562	"Infectious agent detection by nucleic acid (dna or rna); mycobacteria avium-intracellulare, quantification"	"Crosswalk to 87542
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
410	87850	"Infectious agent antigen detection by immunoassay with direct optical (ie, visual) observation; neisseria gonorrhoeae"	"Crosswalk to 87808
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
411	88130	Sex chromatin identification; barr bodies	"Crosswalk to 87209
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
412	88245	"Chromosome analysis for breakage syndromes; baseline sister chromatid exchange (sce), 20-25 cells"	"Crosswalk to 88248
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
413	88741	"Hemoglobin, quantitative, transcutaneous, per day; methemoglobin"	"Crosswalk to 88740
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
414	89330	"Sperm evaluation; cervical mucus penetration test, with or without spinnbarkeit test"	"Crosswalk to 89300
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
415	0173U 	"Psychiatry (ie, depression, anxiety), genomic analysis panel, includes variant analysis of 14 genes"	"Crosswalk to 81418
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
416	0175U 	"Psychiatry (eg, depression, anxiety), genomic analysis panel, variant analysis of 15 genes"	"Crosswalk to 81418
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
417	0392U 	"Drug metabolism (depression, anxiety, attention deficit hyperactivity disorder)"	"Crosswalk to 81418
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
418	0423U 	"Psychiatry (eg, depression, anxiety), genomic analysis panel, including variant analysis"	"Crosswalk to 81418
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
419	0438U 	"Drug metabolism (adverse drug reactions and drug response), buccal specimen, gene-drug interactions"	"Crosswalk to 81418
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
420	0460U 	"Oncology, whole blood or buccal, dna single-nucleotide polymorphism (snp)"	"Crosswalk to 81418
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
421	0461U 	"Oncology, pharmacogenomic analysis of single-nucleotide polymorphism"	"Crosswalk to 81418
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
422	0476U 	"Drug metabolism, psychiatry (eg, major depressive disorder, general anxiety disorder, attention deficit hyperactivity disorder"	"Crosswalk to 81418
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
423	0477U 	"Drug metabolism, psychiatry (eg, major depressive disorder, general anxiety disorder, attention deficit hyperactivity disorder"	"Crosswalk to 81418
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
424	0516U 	"Drug metabolism, whole blood, pharmacogenomic genotyping of 40 genes"	"Crosswalk to 81418
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
425	0533U 	"Drug metabolism (adverse drug reactions and drug response), genotyping of 16 genes"	"Crosswalk to 81418
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
426	0220U 	"Oncology (breast cancer), image analysis with artificial intelligence assessment of 12"	"Crosswalk to 0376U
Crosswalk to 0220U
Gapfill
Abstain"	"10 out of 11
0 out of 11
1 out of 11
0 out of 11"				
427	0261U 	"Oncology (colorectal cancer), image analysis with artificial intelligence assessment of 4 histologic and immunohistochemical features"	"Crosswalk to 0376U
Gapfill
Abstain"	"10 out of 11
1 out of 11
0 out of 11"				
428	0414U 	"Oncology (lung), augmentative algorithmic analysis of digitized whole slide imaging for 8 genes"	"Crosswalk to 0376U
Gapfill
Abstain"	"10 out of 11
1 out of 11
0 out of 11"				
429	0418U 	"Oncology (breast), augmentative algorithmic analysis of digitized whole slide imaging"	"Crosswalk to 0376U
Crosswalk to 0220U
Gapfill
Abstain"	"10 out of 11
0 out of 11
1 out of 11
0 out of 11"				
430	0512U 	"Oncology (prostate), augmentative algorithmic analysis of digitized whole-slide imaging of histologic"	"Crosswalk to 0376U
Gapfill
Abstain"	"10 out of 11
1 out of 11
0 out of 11"				
431	0513U 	"Oncology (prostate), augmentative algorithmic analysis of digitized whole-slide imaging of histologic"	"Crosswalk to 0376U
Gapfill
Abstain"	"10 out of 11
1 out of 11
0 out of 11"				
432	0094U 	"Genome (eg, unexplained constitutional or heritable disorder or syndrome), rapid sequence analysis"	"Crosswalk to 81425 x 1.5
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
433	0426U 	"Genome (eg, unexplained constitutional or heritable disorder or syndrome), ultra-rapid sequence analysis"	"Crosswalk to 81425 x 1.5
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
434	0532U 	"Rare diseases (constitutional disease/hereditary disorders), rapid whole genome and mitochondrial"	"Crosswalk to 81425 x 1.5
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
435	0582U 	"Rare diseases (constitutional disease/hereditary disorders), rapid whole genome"	"Crosswalk to 81425 x 1.5
Gapfill
Abstain"	"10 out of 11
1 out of 11
0 out of 11"				
436	0425U 	"Genome (eg, unexplained constitutional or heritable disorder or syndrome), rapid sequence analysis, each comparator genome"	"Crosswalk to 81426 x 1.5
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
437	0583U 	"Rare diseases (constitutional disease/hereditary disorders), rapid whole genome comparator"	"Crosswalk to 81426 x 1.5
Gapfill
Abstain"	"10 out of 11
0 out of 11
1 out of 11"				
438	0072U 	"Cyp2d6 (cytochrome p450, family 2, subfamily d, polypeptide 6"	"Crosswalk to 81226
Crosswalk to 81238
Abstain"	"2 out of 11
8 out of 11
1 out of 11"				
439	0073U 	"Cyp2d6 (cytochrome p450, family 2, subfamily d, polypeptide 6)"	"Crosswalk to 81226
Crosswalk to 81238
Gapfill
Abstain"	"2 out of 11
8 out of 11
0 out of 11
1 out of 11"				
440	0074U 	"Cyp2d6 (cytochrome p450, family 2, subfamily d, polypeptide 6)"	"Crosswalk to 81226
Crosswalk to 81238
Gapfill
Abstain"	"2 out of 11
8 out of 11
0 out of 11
1 out of 11"				
441	0075U 	"Cyp2d6 (cytochrome p450, family 2, subfamily d, polypeptide 6)"	"Crosswalk to 81226 
Crosswalk to 81238
Gapfill
Abstain"	"2 out of 11
8 out of 11
0 out of 11
1 out of 11"				
442	0076U 	"Cyp2d6 (cytochrome p450, family 2, subfamily d, polypeptide 6)"	"Crosswalk to 81226
Crosswalk to 81238
Gapfill
Abstain"	"2 out of 11
8 out of 11
0 out of 11
1 out of 11"				
443	0365U 	"Oncology (bladder), 10 protein biomarkers (a1at, ang, apoe, ca9, il8, mmp9"	"Crosswalk to 81503
Crosswalk to 0446U
Gapfill
Abstain"	"3 out of 11
8 out of 11
0 out of 11
0 out of 11"				
444	0366U 	"Oncology (bladder), analysis of 10 protein biomarkers (a1at, ang, apoe, ca9, il8, mmp9"	"Crosswalk to 81503 
Crosswalk to 0446U
Gapfill
Abstain"	"3 out of 11
8 out of 11
0 out of 11
0 out of 11"				
445	0367U 	"Oncology (bladder), analysis of 10 protein biomarkers (a1at, ang, apoe, ca9, il8, mmp9, mmp10, pai1, sdc1 and vegfa) by immunoassays"	"Crosswalk to 81503 
Crosswalk to 0446U
Gapfill
Abstain"	"3 out of 11
8 out of 11
0 out of 11
0 out of 11"				
446	0410U 	"Oncology (pancreatic), dna, whole genome sequencing with 5-hydroxymethylcytosine"	"Crosswalk to 81229
Crosswalk to 0410U
Gapfill
Abstain"	"1  out of 11
0 out of 11
10 out of 11
0 out of 11"				
447	0507U 	"Oncology (ovarian), dna, wholegenome sequencing with 5hydroxymethylcytosine"	"Crosswalk to 81229
Crosswalk to 0507U
Gapfill
Abstain"	"1 out of 11
0 out of 11
10 out of 11
0 out of 11"				
448	0565U 	"Oncology (hepatocellular carcinoma), next-generation sequencing methylation"	"Crosswalk to 81229
Gapfill
Abstain"	"2 out of 11
9 out of 11
0 out of 11"				
449	0010U 	"Infectious disease (bacterial), strain typing by whole genome sequencing"	"Crosswalk to 0010U
Crosswalk to 87153 x 3
Gapfill
Abstain"	"0 out of 11
0 out of 11
10 out of 11
1 out of 11"				
450	0140U 	"Infectious disease (fungi), fungal pathogen identification"	"Crosswalk to 87154
Gapfill
Abstain"	"10 out of 11
1 out of 11
0 out of 11"				
451	0224U 	"Antibody, severe acute respiratory syndrome"	"Crosswalk to 86769
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
452	0016U 	"Oncology (hematolymphoid neoplasia), rna, bcr/abl1 major and minor breakpoint"	"Crosswalk to 81206 + 81207
Gapfill
Abstain"	"10 out of 11
1 out of 11
0 out of 11"				
453	0020M 	"Oncology (central nervous system), analysis of 30000 dna methylation loci"	"Crosswalk to 0016M x 0.75
Gapfill
Abstain"	"10 out of 11
0 out of 11
1 out of 11"				
454	0464U 	"Oncology (colorectal) screening, quantitative real-time target and signal amplification"	"Crosswalk to 81327 x 3 + 82274
Crosswalk to 0433U
Crosswalk to 0005U
Crosswalk to 0399U
Crosswalk to 81528
Gapfill
Abstain"	"10 out of 11
0 out of 11
0 out of 11
0 out of 11
0 out of 11
1 out of 11
0 out of 11"				
455	0251U 	"Hepcidin-25, enzyme-linked immunosorbent assay (elisa), serum or plasma"	"Crosswalk to 83520 
Crosswalk to 84305
Gapfill
Abstain"	"1 out of 11
10 out of 11
0 out of 11
0 out of 11"				
456	0390U 	"Obstetrics (preeclampsia), kinase insert domain receptor (kdr), endoglin"	"Crosswalk to 0243U
Crosswalk to 81510
Gapfill
Abstain"	"10 out of 11
1 out of 11
0 out of 11
0 out of 11"				
457	0415U 	"Cardiovascular disease (acute coronary syndrome [acs]), il-16, fas, fasligand, hgf, ctack, eotaxin"	"Crosswalk to 0309U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
458	0445U 	"B-amyloid (abeta42) and phospho tau (181p) (ptau181), electrochemiluminescent immunoassay"	"Crosswalk to 82234 + 84393
Crosswalk to 0445U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11
0 out of 11"				
459	0459U 	"B-amyloid (abeta42) and total tau (ttau), electrochemiluminescent immunoassay"	"Crosswalk to 82234 + 84394
Crosswalk to 0459U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11
0 out of 11"				
460	0462U 	"Melatonin levels test, sleep study, 7 or 9 sample melatonin profile"	"Crosswalk to 82530
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
461	0471U 	"Oncology (colorectal cancer), qualitative real-time pcr of 35 variants"	"Crosswalk to 81275 + 81276 + 81311
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
462	0539U 	"Oncology (solid tumor), cellfree circulating tumor dna (ctdna), 152 genes"	"Crosswalk to 81464
Crosswalk to 0326U
Gapfill
Abstain"	"10 out of 11
1 out of 11
0 out of 11
0 out of 11"				
463	0547U 	"Neurofilament light chain (nfl), chemiluminescent enzyme immunoassay, plasma, quantitative"	"Crosswalk to 0443U
Gapfill
Abstain"	"10 out of 11
0 out of 11
0 out of 11"				
464	0548U 	"Glial fibrillary acidic protein (gfap), chemiluminescent enzyme immunoassay, using plasma"	"Crosswalk to 83884
Gapfill
Abstain"	"10 out of 11
0 out of 11
1 out of 11"				
465	0556U 	Infectious disease (bacterial or viral respiratory tract infection)	"Crosswalk to 87633
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
466	0580U 	Borrelia burgdorferi (lyme disease)	"Crosswalk to 0042U x 2
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11"				
467	0562U 	"Oncology (solid tumor), targeted genomic sequence analysis, 33 genes"	"Crosswalk to 81462
Crosswalk to 0388U
Gapfill
Abstain"	"11 out of 11
0 out of 11
0 out of 11
0 out of 11"				
468	0578U 	"Oncology (cutaneous melanoma), rna, gene expression profiling by realtime qpcr of 10 genes"	"Crosswalk to 81519
Crosswalk to 81529
Gapfill
Abstain"	"10 out of 11
0 out of 11
0 out of 11
1 out of 11"				
469	0596U 	"Neurology (alzheimer disease), plasma, 3 distinct isoform-specific peptides"	"Crosswalk to 81401
Gapfill
Abstain"	"0 out of 11
10 out of 11
1 out of 11"				
470	81188	"Cstb (cystatin b) (eg, unverricht-lundborg disease) gene analysis"	"Crosswalk to 81178
Crosswalk to 81404
Gapfill
Abstain"	"10 out of 11
1 out of 11
0 out of 11
0 out of 11"				
471	87183	Sc std carbapenem resist gen	"Crosswalk to 87150 
Crosswalk to 87150 x 5
Gapfill
Abstain"	"1 out of 11
10 out of 11
0 out of 11
0 out of 11"				
472	87627	Jt spc pthgn&rx rsist gen26+	"Crosswalk to 87507 + 87506
Crosswalk to 87633
Crosswalk to 87627
Crosswalk to 0528U
Gapfill
Abstain"	"1 out of 11
9 out of 11
0 out of 11
0 out of 11
0 out of 11
1 out of 11"				
