CPT Codes

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14,403
Total Codes
14,403
Active
0
Obsolete
0
With Definitions
CPT Codes Directory 14403 codes
Code Preferred Label Status Semantic Types Details
81179
ATXN2 (ataxin 2) (eg, spinocerebellar ataxia) gene analysis, evaluation to detect abnormal (eg, expanded) alleles
Gene analysis (ataxin 2) for abnormal alleles; ATXN2 GENE ANALYSIS EVAL DETECT ABNORMAL ALLELES +1 more
Active
http://purl.bioontology.org/ontology/STY/T059
81180
ATXN3 (ataxin 3) (eg, spinocerebellar ataxia, Machado-Joseph disease) gene analysis, evaluation to detect abnormal (eg, expanded) alleles
ATXN3 GENE ANALYSIS EVAL DETECT ABNORMAL ALLELES; Ataxin 3 (ATXN3) gene analysis for detection of abnormal alleles +1 more
Active
http://purl.bioontology.org/ontology/STY/T059
81181
ATXN7 (ataxin 7) (eg, spinocerebellar ataxia) gene analysis, evaluation to detect abnormal (eg, expanded) alleles
Gene analysis (ataxin 7) for abnormal alleles; ATXN7 GENE ANALYSIS EVAL DETECT ABNORMAL ALLELES +1 more
Active
http://purl.bioontology.org/ontology/STY/T059
81182
ATXN8OS (ATXN8 opposite strand [non-protein coding]) (eg, spinocerebellar ataxia) gene analysis, evaluation to detect abnormal (eg, expanded) alleles
ATXN8OS GENE ANALYSIS EVAL DETECT ABNOR ALLELES; Ataxin 8 opposite strand [non-protein coding] (ATXN8OS) gene analysis for detection of abnormal alleles +1 more
Active
http://purl.bioontology.org/ontology/STY/T059
81183
ATXN10 (ataxin 10) (eg, spinocerebellar ataxia) gene analysis, evaluation to detect abnormal (eg, expanded) alleles
ATXN10 GENE ANALYSIS EVAL DETC ABNORMAL ALLELES; Gene analysis (ataxin 10) for abnormal alleles +1 more
Active
http://purl.bioontology.org/ontology/STY/T059
81184
CACNA1A (calcium voltage-gated channel subunit alpha1 A) (eg, spinocerebellar ataxia) gene analysis; evaluation to detect abnormal (eg, expanded) alleles
Calcium voltage-gated channel subunit alpha1 A (CACNA1A) gene analysis for detection of abnormal alleles; Gene analysis (calcium voltage-gated channel subunit alpha1 A) for abnormal alleles +1 more
Active
http://purl.bioontology.org/ontology/STY/T059
81185
CACNA1A (calcium voltage-gated channel subunit alpha1 A) (eg, spinocerebellar ataxia) gene analysis; full gene sequence
Calcium voltage-gated channel subunit alpha1 A (CACNA1A) full gene sequence analysis; CACNA1A GENE ANALYSIS FULL GENE SEQUENCE +1 more
Active
http://purl.bioontology.org/ontology/STY/T059
81186
CACNA1A (calcium voltage-gated channel subunit alpha1 A) (eg, spinocerebellar ataxia) gene analysis; known familial variant
Gene analysis (calcium voltage-gated channel subunit alpha1 A) for known familial variant; CACNA1A GENE ANALYSIS KNOWN FAMILIAL VARIANT +1 more
Active
http://purl.bioontology.org/ontology/STY/T059
81187
CNBP (CCHC-type zinc finger nucleic acid binding protein) (eg, myotonic dystrophy type 2) gene analysis, evaluation to detect abnormal (eg, expanded) alleles
CNBP GENE ANALYSIS EVAL DETECT ABNORMAL ALLELES; Gene analysis (CCH-type zinc finger nucleic acid binding protein) for abnormal alleles +1 more
Active
http://purl.bioontology.org/ontology/STY/T059
81188
CSTB (cystatin B) (eg, Unverricht-Lundborg disease) gene analysis; evaluation to detect abnormal (eg, expanded) alleles
CSTB GENE ANALYSIS EVAL DETECT ABNORMAL ALLELES; Gene analysis (cystatin B) for abnormal alleles +1 more
Active
http://purl.bioontology.org/ontology/STY/T059
81189
CSTB (cystatin B) (eg, Unverricht-Lundborg disease) gene analysis; full gene sequence
CSTB GENE ANALYSIS FULL GENE SEQUENCE; Gene analysis (cystatin B) of full sequence +1 more
Active
http://purl.bioontology.org/ontology/STY/T059
81190
CSTB (cystatin B) (eg, Unverricht-Lundborg disease) gene analysis; known familial variant(s)
Gene analysis (cystatin B) for known familial variants; CSTB GENE ANALYSIS KNOWN FAMILIAL VARIANTS +1 more
Active
http://purl.bioontology.org/ontology/STY/T059
81200
ASPA (aspartoacylase) (eg, Canavan disease) gene analysis, common variants (eg, E285A, Y231X)
Aspartoacylase (ASPA) gene analysis for detection of E285A variant; Gene analysis (aspartoacylase) +4 more
Active
http://purl.bioontology.org/ontology/STY/T059
81201
APC (adenomatous polyposis coli) (eg, familial adenomatosis polyposis [FAP], attenuated FAP) gene analysis; full gene sequence
Familial adenomatous polyposis coli (APC) full gene sequence analysis; Gene analysis (adenomatous polyposis coli), full gene sequence +3 more
Active
http://purl.bioontology.org/ontology/STY/T059
81202
APC (adenomatous polyposis coli) (eg, familial adenomatosis polyposis [FAP], attenuated FAP) gene analysis; known familial variants
Familial adenomatous polyposis coli (APC) gene analysis for detection of known familial variants; APC GENE ANALYSIS KNOWN FAMILIAL VARIANTS +3 more
Active
http://purl.bioontology.org/ontology/STY/T059
81203
APC (adenomatous polyposis coli) (eg, familial adenomatosis polyposis [FAP], attenuated FAP) gene analysis; duplication/deletion variants
Adenomatous polyposis coli (APC) gene analysis for detection of deletion and duplication variants; APC GENE ANALYSIS DUPLICATION/DELETION VARIANTS +3 more
Active
http://purl.bioontology.org/ontology/STY/T059
81204
AR (androgen receptor) (eg, spinal and bulbar muscular atrophy, Kennedy disease, X chromosome inactivation) gene analysis; characterization of alleles (eg, expanded size or methylation status)
Androgen receptor (AR) gene analysis for characterization of alleles; Gene analysis (androgen receptor) for characterization of alleles +1 more
Active
http://purl.bioontology.org/ontology/STY/T059
81205
BCKDHB (branched-chain keto acid dehydrogenase E1, beta polypeptide) (eg, maple syrup urine disease) gene analysis, common variants (eg, R183P, G278S, E422X)
Branched-chain keto acid dehydrogenase E1, beta polypeptide (BCKDHB) gene analysis for detection of E422X variant; Gene analysis (branched-chain keto acid dehydrogenase E1, beta polypeptide) +5 more
Active
http://purl.bioontology.org/ontology/STY/T059
81206
BCR/ABL1 (t(9;22)) (eg, chronic myelogenous leukemia) translocation analysis; major breakpoint, qualitative or quantitative
Qualitative t(9;22) (BCR/ABL1) translocation analysis for detection of major breakpoint; Translocation analysis (BCR/ABL1) minor breakpoint +2 more
Active
http://purl.bioontology.org/ontology/STY/T059
81207
BCR/ABL1 (t(9;22)) (eg, chronic myelogenous leukemia) translocation analysis; minor breakpoint, qualitative or quantitative
Qualitative t(9;22) (BCR/ABL1) translocation analysis for detection of minor breakpoint; Quantitative t(9;22) (BCR/ABL1) translocation analysis for detection of minor breakpoint +2 more
Active
http://purl.bioontology.org/ontology/STY/T059
81208
BCR/ABL1 (t(9;22)) (eg, chronic myelogenous leukemia) translocation analysis; other breakpoint, qualitative or quantitative
BCR/ABL1 OTHER BREAKPNT QUALITATIVE/QUANTITATIVE; Quantitative t(9;22) (BCR/ABL1) translocation analysis for detection of breakpoint +2 more
Active
http://purl.bioontology.org/ontology/STY/T059
81209
BLM (Bloom syndrome, RecQ helicase-like) (eg, Bloom syndrome) gene analysis, 2281del6ins7 variant
Gene analysis (Bloom syndrome, RecQ helicase-like); BLM GENE ANALYSIS 2281DEL6INS7 VARIANT +1 more
Active
http://purl.bioontology.org/ontology/STY/T059
81210
BRAF (B-Raf proto-oncogene, serine/threonine kinase) (eg, colon cancer, melanoma), gene analysis, V600 variant(s)
Gene analysis (v-raf murine sarcoma viral oncogene homolog B1); BRAF GENE ANALYSIS V600 VARIANT(S) +1 more
Active
http://purl.bioontology.org/ontology/STY/T059
81212
BRCA1 (BRCA1, DNA repair associated), BRCA2 (BRCA2, DNA repair associated) (eg, hereditary breast and ovarian cancer) gene analysis; 185delAG, 5385insC, 6174delT variants
Breast cancer 1 and 2 (BRCA1, BRCA2) gene analysis for detection of 185delAG variant; BRCA1 BRCA 2 GEN ALYS 185DELAG 5385INSC 6174DELT +4 more
Active
http://purl.bioontology.org/ontology/STY/T059
81215
BRCA1 (BRCA1, DNA repair associated) (eg, hereditary breast and ovarian cancer) gene analysis; known familial variant
Breast cancer 1 (BRCA1) gene analysis for detection of known familial variant; BRCA1 GENE ANALYSIS KNOWN FAMILIAL VARIANT +1 more
Active
http://purl.bioontology.org/ontology/STY/T059
81216
BRCA2 (BRCA2, DNA repair associated) (eg, hereditary breast and ovarian cancer) gene analysis; full sequence analysis
BRCA2 GENE ANALYSIS FULL SEQUENCE ANALYSIS; Gene analysis (breast cancer 2) of full sequence +1 more
Active
http://purl.bioontology.org/ontology/STY/T059
81217
BRCA2 (BRCA2, DNA repair associated) (eg, hereditary breast and ovarian cancer) gene analysis; known familial variant
Breast cancer 2 (BRCA2) gene analysis for detection of known familial variant; BRCA2 GENE ANALYSIS KNOWN FAMILIAL VARIANT +1 more
Active
http://purl.bioontology.org/ontology/STY/T059
81218
CEBPA (CCAAT/enhancer binding protein [C/EBP], alpha) (eg, acute myeloid leukemia), gene analysis, full gene sequence
Gene analysis (ccaat/enhancer binding protein [c/ebp], alpha) full gene sequence; CCAAT/enhancer binding protein [C/EBP], alpha (CEBPA) full gene sequence analysis +1 more
Active
http://purl.bioontology.org/ontology/STY/T059
81219
CALR (calreticulin) (eg, myeloproliferative disorders), gene analysis, common variants in exon 9
CALR GENE ANALYSIS COMMON VARIANTS IN EXON 9; Gene analysis (calreticulin), common variants +1 more
Active
http://purl.bioontology.org/ontology/STY/T059
81220
CFTR (cystic fibrosis transmembrane conductance regulator) (eg, cystic fibrosis) gene analysis; common variants (eg, ACMG/ACOG guidelines)
Gene analysis (cystic fibrosis transmembrane conductance regular) common variants; CFTR GENE ANALYSIS COMMON VARIANTS +1 more
Active
http://purl.bioontology.org/ontology/STY/T059
81221
CFTR (cystic fibrosis transmembrane conductance regulator) (eg, cystic fibrosis) gene analysis; known familial variants
Gene analysis (cystic fibrosis transmembrane conductance regular) known familial variants; Cystic fibrosis transmembrane conductance regulator (CFTR) gene analysis for detection of known familial variant +1 more
Active
http://purl.bioontology.org/ontology/STY/T059
81222
CFTR (cystic fibrosis transmembrane conductance regulator) (eg, cystic fibrosis) gene analysis; duplication/deletion variants
Cystic fibrosis transmembrane conductance regulator (CFTR) gene analysis for detection of duplication variant; Cystic fibrosis transmembrane conductance regulator (CFTR) gene analysis for detection of deletion variant +2 more
Active
http://purl.bioontology.org/ontology/STY/T059
81223
CFTR (cystic fibrosis transmembrane conductance regulator) (eg, cystic fibrosis) gene analysis; full gene sequence
Cystic fibrosis transmembrane conductance regulator (CFTR) full sequence gene analysis; Gene analysis (cystic fibrosis transmembrane conductance regular) full gene sequence +1 more
Active
http://purl.bioontology.org/ontology/STY/T059
81224
CFTR (cystic fibrosis transmembrane conductance regulator) (eg, cystic fibrosis) gene analysis; intron 8 poly-T analysis (eg, male infertility)
Gene analysis (cystic fibrosis transmembrane conductance regular) intron 8 poly-T; Cystic fibrosis transmembrane conductance regulator (CFTR) gene analysis with intron 8 poly-T analysis +1 more
Active
http://purl.bioontology.org/ontology/STY/T059
81225
CYP2C19 (cytochrome P450, family 2, subfamily C, polypeptide 19) (eg, drug metabolism), gene analysis, common variants (eg, *2, *3, *4, *8, *17)
Cytochrome P450, family 2, subfamily C, polypeptide 19 (CYP2C19) gene analysis for detection of *2 variant; CYP2C19 GENE ANALYSIS COMMON VARIANTS +6 more
Active
http://purl.bioontology.org/ontology/STY/T059
81226
CYP2D6 (cytochrome P450, family 2, subfamily D, polypeptide 6) (eg, drug metabolism), gene analysis, common variants (eg, *2, *3, *4, *5, *6, *9, *10, *17, *19, *29, *35, *41, *1XN, *2XN, *4XN)
Gene analysis (cytochrome P450, family 2, subfamily D, polypeptide 6) common variants; Cytochrome P450, family 2, subfamily D, polypeptide 6 (CYP2D6) gene analysis for detection of *29 variant +16 more
Active
http://purl.bioontology.org/ontology/STY/T059
81227
CYP2C9 (cytochrome P450, family 2, subfamily C, polypeptide 9) (eg, drug metabolism), gene analysis, common variants (eg, *2, *3, *5, *6)
CYP2C9 GENE ANALYSIS COMMON VARIANTS; Cytochrome P450, family 2, subfamily C, polypeptide 9 (CYP2C9) gene analysis for detection of *3 variant +5 more
Active
http://purl.bioontology.org/ontology/STY/T059
81228
Cytogenomic constitutional (genome-wide) microarray analysis; interrogation of genomic regions for copy number variants (eg, bacterial artificial chromosome [BAC] or oligo-based comparative genomic hybridization [CGH] microarray analysis)
Oligo-based comparative genomic hybridization [CGH] constitutional microarray analysis with interrogation of genomic region for detection of copy number variant; Oligo-based comparative genomic hybridization [CGH] constitutional microarray analysis +6 more
Active
http://purl.bioontology.org/ontology/STY/T059
81229
Cytogenomic constitutional (genome-wide) microarray analysis; interrogation of genomic regions for copy number and single nucleotide polymorphism (SNP) variants for chromosomal abnormalities
CYTOGENOM CONST MICROARRAY COPY NUMBER&SNP VAR; Genome-wide microarray analysis for copy number and single nucleotide polymorphism variants +3 more
Active
http://purl.bioontology.org/ontology/STY/T059
81230
CYP3A4 (cytochrome P450 family 3 subfamily A member 4) (eg, drug metabolism), gene analysis, common variant(s) (eg, *2, *22)
CYP3A4 GENE ANALYSIS COMMON VARIANTS; Cytochrome P450 family 3 subfamily A member 4 (CYP3A4) gene analysis for detection of *22 variant +3 more
Active
http://purl.bioontology.org/ontology/STY/T059
81231
CYP3A5 (cytochrome P450 family 3 subfamily A member 5) (eg, drug metabolism), gene analysis, common variants (eg, *2, *3, *4, *5, *6, *7)
Cytochrome P450 family 3 subfamily A member 5 (CYP3A5) gene analysis for detection of *2, *3, *4, *5 *6, and *7 variants; Gene analysis (cytochrome P450 family 3 subfamily A member 5) for common variant +2 more
Active
http://purl.bioontology.org/ontology/STY/T059
81232
DPYD (dihydropyrimidine dehydrogenase) (eg, 5-fluorouracil/5-FU and capecitabine drug metabolism), gene analysis, common variant(s) (eg, *2A, *4, *5, *6)
Dihydropyrimidine dehydrogenase (DPYD) gene analysis for detection of *5 variant; Dihydropyrimidine dehydrogenase (DPYD) gene analysis for detection of *2A variant +5 more
Active
http://purl.bioontology.org/ontology/STY/T059
81233
BTK (Bruton's tyrosine kinase) (eg, chronic lymphocytic leukemia) gene analysis, common variants (eg, C481S, C481R, C481F)
Gene analysis (Bruton's tyrosine kinase) for common variants; BTK GENE ANALYSIS COMMON VARIANTS +1 more
Active
http://purl.bioontology.org/ontology/STY/T059
81234
DMPK (DM1 protein kinase) (eg, myotonic dystrophy type 1) gene analysis; evaluation to detect abnormal (expanded) alleles
Gene analysis (DM1 protein kinase) for abnormal alleles; DMPK GENE ANALYSIS EVAL DETECT ABNORMAL ALLELES +1 more
Active
http://purl.bioontology.org/ontology/STY/T059
81235
EGFR (epidermal growth factor receptor) (eg, non-small cell lung cancer) gene analysis, common variants (eg, exon 19 LREA deletion, L858R, T790M, G719A, G719S, L861Q)
EGFR gene analysis for T790M variant; EGFR gene analysis for G719S variant +7 more
Active
http://purl.bioontology.org/ontology/STY/T059
81236
EZH2 (enhancer of zeste 2 polycomb repressive complex 2 subunit) (eg, myelodysplastic syndrome, myeloproliferative neoplasms) gene analysis, full gene sequence
Gene analysis (enhancer of zeste 2 polycomb repressive complex 2 subunit) of full sequence; Enhancer of zeste 2 polycomb repressive complex 2 subunit (EZH2) full sequence gene analysis +1 more
Active
http://purl.bioontology.org/ontology/STY/T059
81237
EZH2 (enhancer of zeste 2 polycomb repressive complex 2 subunit) (eg, diffuse large B-cell lymphoma) gene analysis, common variant(s) (eg, codon 646)
Enhancer of zeste 2 polycomb repressive complex 2 subunit (EZH2) gene analysis for detection of common variants; EZH2 GENE ANALYSIS COMMON VARIANTS +1 more
Active
http://purl.bioontology.org/ontology/STY/T059
81238
F9 (coagulation factor IX) (eg, hemophilia B), full gene sequence
Gene analysis (coagulation factor IX) full sequence analysis; F9 FULL GENE SEQUENCE +1 more
Active
http://purl.bioontology.org/ontology/STY/T059
81239
DMPK (DM1 protein kinase) (eg, myotonic dystrophy type 1) gene analysis; characterization of alleles (eg, expanded size)
DMPK GENE ANALYSIS CHARACTERIZATION OF ALLELES; Gene analysis (DM1 protein kinase) for characterization of alleles +1 more
Active
http://purl.bioontology.org/ontology/STY/T059
81240
F2 (prothrombin, coagulation factor II) (eg, hereditary hypercoagulability) gene analysis, 20210G>A variant
F2 GENE ANALYSIS 20210G >A VARIANT; Gene analysis (prothrombin, coagulation factor II) A variant +1 more
Active
http://purl.bioontology.org/ontology/STY/T059
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