CPT Codes
CMS14,403
Total Codes
14,403
Active
0
Obsolete
0
With Definitions
CPT Codes Directory
14403 codes
| Code | Preferred Label | Status | Semantic Types | Details |
|---|---|---|---|---|
| 81296 |
MSH2 (mutS homolog 2, colon cancer, nonpolyposis type 1) (eg, hereditary non-polyposis colorectal cancer, Lynch syndrome) gene analysis; known familial variants
MSH2 GENE ANALYSIS KNOWN FAMILIAL VARIANTS; MutS homolog 2, colon cancer, nonpolyposis type 1 (MSH2) gene analysis for detection of known familial variant
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81297 |
MSH2 (mutS homolog 2, colon cancer, nonpolyposis type 1) (eg, hereditary non-polyposis colorectal cancer, Lynch syndrome) gene analysis; duplication/deletion variants
Gene analysis (mutS homolog 2, colon cancer, nonpolyposis type 1) duplication or deletion variants; MutS homolog 2, colon cancer, nonpolyposis type 1 (MSH2) gene analysis for detection of deletion and duplication variants
+3 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81298 |
MSH6 (mutS homolog 6 [E. coli]) (eg, hereditary non-polyposis colorectal cancer, Lynch syndrome) gene analysis; full sequence analysis
MSH6 GENE ANALYSIS FULL SEQUENCE ANALYSIS; MutS homolog 6 (E. coli) (MSH6) full gene sequence analysis
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81299 |
MSH6 (mutS homolog 6 [E. coli]) (eg, hereditary non-polyposis colorectal cancer, Lynch syndrome) gene analysis; known familial variants
MutS homolog 6 (E. coli) (MSH6) gene analysis for detection of known familial variant; Gene analysis (mutS homolog 6 [E coli]) known familial variants
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81300 |
MSH6 (mutS homolog 6 [E. coli]) (eg, hereditary non-polyposis colorectal cancer, Lynch syndrome) gene analysis; duplication/deletion variants
MSH6 GENE ANALYSIS DUPLICATION/DELETION VARIA; Gene analysis (mutS homolog 6 [E coli]) duplication or deletion variants
+3 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81301 |
Microsatellite instability analysis (eg, hereditary non-polyposis colorectal cancer, Lynch syndrome) of markers for mismatch repair deficiency (eg, BAT25, BAT26), includes comparison of neoplastic and normal tissue, if performed
Microsatellite instability analysis of markers for mismatch repair deficiency with comparison of neoplastic and normal tissue; MICROSATELLITE INSTAB ANAL MISMATCH REPAIR DEF
+8 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
http://purl.bioontology.org/ontology/STY/T063
|
|
| 81302 |
MECP2 (methyl CpG binding protein 2) (eg, Rett syndrome) gene analysis; full sequence analysis
Gene analysis (methyl CpG binding protein 2) full sequence analysis; MECP2 GENE ANALYSIS FULL SEQUENCE
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81303 |
MECP2 (methyl CpG binding protein 2) (eg, Rett syndrome) gene analysis; known familial variant
Methyl CpG binding protein 2 (MECP2) gene analysis for detection of known familial variant; Gene analysis (methyl CpG binding protein 2) known familial variant
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81304 |
MECP2 (methyl CpG binding protein 2) (eg, Rett syndrome) gene analysis; duplication/deletion variants
MECP2 GENE ANALYSIS DUPLICATION/DELETION VARIANT; Methyl CpG binding protein 2 (MECP2) gene analysis for detection of deletion and duplication variants
+3 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81305 |
MYD88 (myeloid differentiation primary response 88) (eg, Waldenstrom's macroglobulinemia, lymphoplasmacytic leukemia) gene analysis, p.Leu265Pro (L265P) variant
MYD88 GENE ANALYSIS P.LEU265 (L265P) VARIANT; Myeloid differentiation primary response 88 (MYD88) gene analysis for detection of p.Leu265Pro (L265P) variant
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81306 |
NUDT15 (nudix hydrolase 15) (eg, drug metabolism) gene analysis, common variant(s) (eg, *2, *3, *4, *5, *6)
NUDT15 GENE ANALYSIS COMMON VARIANTS; Nudix hydrolase 15 (NUDT15) gene analysis for detection of common variants
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81307 |
PALB2 (partner and localizer of BRCA2) (eg, breast and pancreatic cancer) gene analysis; full gene sequence
Gene analysis (partner and localizer of BRCA2) full sequence analysis; PALB2 GENE ANALYSIS FULL GENE SEQUENCE
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81308 |
PALB2 (partner and localizer of BRCA2) (eg, breast and pancreatic cancer) gene analysis; known familial variant
PALB2 GENE ANALYSIS KNOWN FAMILIAL VARIANT; Gene analysis (partner and localizer of BRCA2) for detection of known familial variant
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81309 |
PIK3CA (phosphatidylinositol-4, 5-biphosphate 3-kinase, catalytic subunit alpha) (eg, colorectal and breast cancer) gene analysis, targeted sequence analysis (eg, exons 7, 9, 20)
Phosphatidylinositol-4, 5-biphosphate 3-kinase, catalytic subunit alpha (PIK3CA) targeted sequence analysis of exons 20; Phosphatidylinositol-4, 5-biphosphate 3-kinase, catalytic subunit alpha (PIK3CA) targeted sequence analysis of exon 7
+5 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81310 |
NPM1 (nucleophosmin) (eg, acute myeloid leukemia) gene analysis, exon 12 variants
Gene analysis (nucleophosmin) exon 12 variants; NPM1 NUCLEOPHOSMIN GENE ANAL EXON 12 VARIANTS
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81311 |
NRAS (neuroblastoma RAS viral [v-ras] oncogene homolog) (eg, colorectal carcinoma), gene analysis, variants in exon 2 (eg, codons 12 and 13) and exon 3 (eg, codon 61)
Gene analysis for cancer (neuroblastoma); NRAS GENE ANALYSIS VARIANTS IN EXON 2&3
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81312 |
PABPN1 (poly[A] binding protein nuclear 1) (eg, oculopharyngeal muscular dystrophy) gene analysis, evaluation to detect abnormal (eg, expanded) alleles
Gene analysis (poly[A] binding protein nuclear 1) for abnormal alleles; PABPN1 GENE ANALYSIS EVAL DETC ABNORMAL ALLELES
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81313 |
PCA3/KLK3 (prostate cancer antigen 3 [non-protein coding]/kallikrein-related peptidase 3 [prostate specific antigen]) ratio (eg, prostate cancer)
Measurement of PCA3/KLK3 (prostate cancer antigen 3 and kallikrein-related peptidase 3) ratio; Test for detecting genes associated with prostate cancer
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81314 |
PDGFRA (platelet-derived growth factor receptor, alpha polypeptide) (eg, gastrointestinal stromal tumor [GIST]), gene analysis, targeted sequence analysis (eg, exons 12, 18)
PDGFRA GENE ANALYS TARGETED SEQUENCE ANALYS; Platelet-derived growth factor receptor, alpha polypeptide (PDGFRA) gene analysis, targeted sequence analysis
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81315 |
PML/RARalpha, (t(15;17)), (promyelocytic leukemia/retinoic acid receptor alpha) (eg, promyelocytic leukemia) translocation analysis; common breakpoints (eg, intron 3 and intron 6), qualitative or quantitative
Quantitative promyelocytic leukemia/retinoic acid receptor alpha (PML/RARalpha) translocation analysis for detection of intron 6 breakpoint; Qualitative promyelocytic leukemia/retinoic acid receptor alpha (PML/RARalpha) translocation analysis for detection of intron 3 breakpoint
+6 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81316 |
PML/RARalpha, (t(15;17)), (promyelocytic leukemia/retinoic acid receptor alpha) (eg, promyelocytic leukemia) translocation analysis; single breakpoint (eg, intron 3, intron 6 or exon 6), qualitative or quantitative
Quantitative promyelocytic leukemia/retinoic acid receptor alpha (PML/RARalpha) translocation analysis for detection of single exon 6 breakpoint; Quantitative promyelocytic leukemia/retinoic acid receptor alpha (PML/RARalpha) translocation analysis for detection of single breakpoint
+8 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81317 |
PMS2 (postmeiotic segregation increased 2 [S. cerevisiae]) (eg, hereditary non-polyposis colorectal cancer, Lynch syndrome) gene analysis; full sequence analysis
Gene analysis (postmeiotic segregation increased 2 [S cerevisiae]) full sequence analysis; PMS2 GENE ANALYSIS FULL SEQUENCE
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81318 |
PMS2 (postmeiotic segregation increased 2 [S. cerevisiae]) (eg, hereditary non-polyposis colorectal cancer, Lynch syndrome) gene analysis; known familial variants
PMS2 GENE ANALYSIS KNOWN FAMILIAL VARIANTS; Gene analysis (postmeiotic segregation increased 2 [S cerevisiae]) known familiar variants
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81319 |
PMS2 (postmeiotic segregation increased 2 [S. cerevisiae]) (eg, hereditary non-polyposis colorectal cancer, Lynch syndrome) gene analysis; duplication/deletion variants
Postmeiotic segregation increased 2 (PMS2) gene analysis for detection of deletion variant; PMS2 GENE ANALYSIS DUPLICATION/DELETION VARIANTS
+3 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81320 |
PLCG2 (phospholipase C gamma 2) (eg, chronic lymphocytic leukemia) gene analysis, common variants (eg, R665W, S707F, L845F)
PLCG2 GENE ANALYSIS COMMON VARIANTS; Phospholipase C gamma 2 (PLCG2) gene analysis for detection of common variants
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81321 |
PTEN (phosphatase and tensin homolog) (eg, Cowden syndrome, PTEN hamartoma tumor syndrome) gene analysis; full sequence analysis
Phosphatase and tensin homolog (PTEN) full gene sequence analysis; Gene analysis (phosphatase and tensin homolog), full sequence analysis
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81322 |
PTEN (phosphatase and tensin homolog) (eg, Cowden syndrome, PTEN hamartoma tumor syndrome) gene analysis; known familial variant
Phosphatase and tensin homolog (PTEN) gene analysis for known familial variant; PTEN GENE ANALYSIS KNOWN FAMILIAL VARIANT
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81323 |
PTEN (phosphatase and tensin homolog) (eg, Cowden syndrome, PTEN hamartoma tumor syndrome) gene analysis; duplication/deletion variant
Phosphatase and tensin homolog (PTEN) gene analysis for duplication variant; Phosphatase and tensin homolog (PTEN) gene analysis for deletion and duplication variants
+3 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81324 |
PMP22 (peripheral myelin protein 22) (eg, Charcot-Marie-Tooth, hereditary neuropathy with liability to pressure palsies) gene analysis; duplication/deletion analysis
Peripheral myelin protein 22 (PMP22) gene analysis for duplication variant; Peripheral myelin protein 22 (PMP22) gene analysis for deletion variant
+3 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81325 |
PMP22 (peripheral myelin protein 22) (eg, Charcot-Marie-Tooth, hereditary neuropathy with liability to pressure palsies) gene analysis; full sequence analysis
Peripheral myelin protein 22 (PMP22) full gene sequence analysis; PMP22 GENE ANALYSIS FULL SEQUENCE ANALYSIS
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81326 |
PMP22 (peripheral myelin protein 22) (eg, Charcot-Marie-Tooth, hereditary neuropathy with liability to pressure palsies) gene analysis; known familial variant
Gene analysis (peripheral myelin protein 22), known familial variant; Peripheral myelin protein 22 (PMP22) gene analysis for known familial variant
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81327 |
SEPT9 (Septin9) (eg, colorectal cancer) promoter methylation analysis
SEPT9 (Septin9) promoter methylation analysis; SEPT9 GENE PROMOTER METHYLATION ANALYSIS
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81328 |
SLCO1B1 (solute carrier organic anion transporter family, member 1B1) (eg, adverse drug reaction), gene analysis, common variant(s) (eg, *5)
Solute carrier organic anion transporter family, member 1B1 (SLCO1B1) gene analysis for detection of *5 variant; SLCO1B1 GENE ANALYSIS COMMON VARIANTS
+2 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81329 |
SMN1 (survival of motor neuron 1, telomeric) (eg, spinal muscular atrophy) gene analysis; dosage/deletion analysis (eg, carrier testing), includes SMN2 (survival of motor neuron 2, centromeric) analysis, if performed
Survival of motor neuron 1, telomeric (SMN1) dosage/deletion analysis; Survival of motor neuron 1, telomeric (SMN1) dosage/deletion analysis and survival of motor neuron 2, centromeric (SMN2) gene analysis
+2 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81330 |
SMPD1(sphingomyelin phosphodiesterase 1, acid lysosomal) (eg, Niemann-Pick disease, Type A) gene analysis, common variants (eg, R496L, L302P, fsP330)
SMPD1 GENE ANALYSIS COMMON VARIANTS; Gene analysis (sphingomyelin phosphodiesterase 1, acid lysosomal) common variants
+5 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81331 |
SNRPN/UBE3A (small nuclear ribonucleoprotein polypeptide N and ubiquitin protein ligase E3A) (eg, Prader-Willi syndrome and/or Angelman syndrome), methylation analysis
SNRPN/UBE3A METHYLATION ANALYSIS; Small nuclear ribonucleoprotein polypeptide N and ubiquitin protein ligase E3A (SNRPN/UBE3A gene analysis for detection of methylated variant
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81332 |
SERPINA1 (serpin peptidase inhibitor, clade A, alpha-1 antiproteinase, antitrypsin, member 1) (eg, alpha-1-antitrypsin deficiency), gene analysis, common variants (eg, *S and *Z)
SERPINA1 GENE ANALYSIS COMMON VARIANTS; Serpin peptidase inhibitor, clade A, alpha-1 antiproteinase, antitrypsin, member 1 (SERPINA1) gene analysis for detection of *Z variant
+4 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81333 |
TGFBI (transforming growth factor beta-induced) (eg, corneal dystrophy) gene analysis, common variants (eg, R124H, R124C, R124L, R555W, R555Q)
Transforming growth factor beta-induced (TGFBI) gene analysis for detection of common variants; Gene analysis (transforming growth factor beta-induced) for common variants
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81334 |
RUNX1 (runt related transcription factor 1) (eg, acute myeloid leukemia, familial platelet disorder with associated myeloid malignancy) gene analysis, targeted sequence analysis (eg, exons 3-8)
Runt related transcription factor 1 (RUNX1) gene analysis of targeted sequence; Runt related transcription factor 1 (RUNX1) gene analysis of exons 3-8
+2 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81335 |
TPMT (thiopurine S-methyltransferase) (eg, drug metabolism), gene analysis, common variants (eg, *2, *3)
Thiopurine S-methyltransferase (TPMT) gene analysis for detection of *2 and *3 variants; Gene analysis (thiopurine S-methyltransferase) for common variant
+2 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81336 |
SMN1 (survival of motor neuron 1, telomeric) (eg, spinal muscular atrophy) gene analysis; full gene sequence
Gene analysis (survival of motor neuron 1, telomeric) of full sequence; Survival of motor neuron 1, telomeric (SMN1) full sequence gene analysis
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81337 |
SMN1 (survival of motor neuron 1, telomeric) (eg, spinal muscular atrophy) gene analysis; known familial sequence variant(s)
SMN1 GENE ANALYSIS KNOWN FAMILIAL SEQ VARIANTS; Gene analysis (survival of motor neuron 1, telomeric) for known familial sequence variants
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81340 |
TRB@ (T cell antigen receptor, beta) (eg, leukemia and lymphoma), gene rearrangement analysis to detect abnormal clonal population(s); using amplification methodology (eg, polymerase chain reaction)
TRB@ REARRANGEMENT ANAL AMPLIFICATION METHOD; Beta T cell antigen receptor (TRB@) gene rearrangement analysis for detection of abnormal clonal population, using amplification method
+2 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 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)
Beta T cell antigen receptor (TRB@) gene rearrangement analysis for detection of abnormal clonal population, using direct probe method; Beta T cell antigen receptor (TRB@) gene rearrangement analysis for detection of abnormal clonal population, using Southern blot method
+2 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81342 |
TRG@ (T cell antigen receptor, gamma) (eg, leukemia and lymphoma), gene rearrangement analysis, evaluation to detect abnormal clonal population(s)
Gamma T cell antigen receptor (TRG@) gene rearrangement analysis for detection of abnormal clonal population; Gene rearrangement analysis detection abnormal clonal population (T cell antigen receptor gamma)
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81343 |
PPP2R2B (protein phosphatase 2 regulatory subunit Bbeta) (eg, spinocerebellar ataxia) gene analysis, evaluation to detect abnormal (eg, expanded) alleles
Protein phosphatase 2 regulatory subunit Bbeta (PPP2R2B) gene analysis for detection of abnormal alleles; PPP2R2B GENE ANALYSIS EVAL DETC ABNORMAL ALLELES
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81344 |
TBP (TATA box binding protein) (eg, spinocerebellar ataxia) gene analysis, evaluation to detect abnormal (eg, expanded) alleles
Gene analysis (TATA box binding protein) for abnormal alleles; TBP GENE ANALYSIS EVAL DETECT ABNORMAL ALLELES
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81345 |
TERT (telomerase reverse transcriptase) (eg, thyroid carcinoma, glioblastoma multiforme) gene analysis, targeted sequence analysis (eg, promoter region)
TERT GENE ANALYSIS TARGETED SEQUENCE ANALYSIS; Gene analysis (telomerase reverse transcriptase) targeted sequence analysis
+2 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81346 |
TYMS (thymidylate synthetase) (eg, 5-fluorouracil/5-FU drug metabolism), gene analysis, common variant(s) (eg, tandem repeat variant)
Thymidylate synthetase (TYMS) gene analysis for detection of common variant; TYMS GENE ANALYSIS COMMON VARIANTS
+2 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81350 |
UGT1A1 (UDP glucuronosyltransferase 1 family, polypeptide A1) (eg, drug metabolism, hereditary unconjugated hyperbilirubinemia [Gilbert syndrome]) gene analysis, common variants (eg, *28, *36, *37)
UDP glucuronosyltransferase 1 family, polypeptide A1 (UGT1A1) gene analysis for detection of *36 variant; Gene analysis (UDP glucuronosyltransferase 1 family, polypeptide A1) for detection of common variants
+3 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|