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 |
|---|---|---|---|---|
| 81355 |
VKORC1 (vitamin K epoxide reductase complex, subunit 1) (eg, warfarin metabolism), gene analysis, common variant(s) (eg, -1639G>A, c.173+1000C>T)
Vitamin K epoxide reductase complex, subunit 1 (VKORC1) gene analysis for detection of common variant; VKORC1 GENE ANALYSIS COMMON VARIANT(S)
+2 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81361 |
HBB (hemoglobin, subunit beta) (eg, sickle cell anemia, beta thalassemia, hemoglobinopathy); common variant(s) (eg, HbS, HbC, HbE)
Hemoglobin, subunit beta (HBB) gene analysis for detection of HbC variant; Gene analysis (hemoglobin, subunit beta) for common variant
+4 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81362 |
HBB (hemoglobin, subunit beta) (eg, sickle cell anemia, beta thalassemia, hemoglobinopathy); known familial variant(s)
HBB KNOWN FAMILIAL VARIANTS; Gene analysis (hemoglobin, subunit beta) for known familial variant
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81363 |
HBB (hemoglobin, subunit beta) (eg, sickle cell anemia, beta thalassemia, hemoglobinopathy); duplication/deletion variant(s)
Gene analysis (hemoglobin, subunit beta) for duplication/deletion variant; HBB DUPLICATION/DELETION VARIANTS
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81364 |
HBB (hemoglobin, subunit beta) (eg, sickle cell anemia, beta thalassemia, hemoglobinopathy); full gene sequence
Gene analysis (hemoglobin, subunit beta) full sequence analysis; HBB (hemoglobin, subunit beta) full gene sequence analysis
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81370 |
HLA Class I and II typing, low resolution (eg, antigen equivalents); HLA-A, -B, -C, -DRB1/3/4/5, and -DQB1
HLA class I and II typing low resolution HLA-A, -B, -C, -DRB1/3/4/5 and -DQB1; Low resolution human leukocyte antigen (HLA) Class I and II typing of HLA-A, HLA-B, HLA-C, HLA-DRB1/3/4/5, and HLA-DQB1
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81371 |
HLA Class I and II typing, low resolution (eg, antigen equivalents); HLA-A, -B, and -DRB1 (eg, verification typing)
HLA class I and II typing, low resolution HLA-A, -B, and -DRB1; HLA I&LI LOW RESOLUTION HLA-A -B&-DRB1
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81372 |
HLA Class I typing, low resolution (eg, antigen equivalents); complete (ie, HLA-A, -B, and -C)
HLA class I typing low resolution; Complete low resolution human leukocyte antigen (HLA) Class I typing
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81373 |
HLA Class I typing, low resolution (eg, antigen equivalents); one locus (eg, HLA-A, -B, or -C), each
HLA class I typing low resolution one locus; Low resolution human leukocyte antigen (HLA) Class I typing of HLA-A
+4 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81374 |
HLA Class I typing, low resolution (eg, antigen equivalents); one antigen equivalent (eg, B*27), each
HLA class I typing, low resolution one antigen equivalent; Low resolution human leukocyte antigen (HLA) Class I typing of antigen equivalent
+2 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81375 |
HLA Class II typing, low resolution (eg, antigen equivalents); HLA-DRB1/3/4/5 and -DQB1
HLA II LOW RESOLUTION HLA-DRB1/3/4/5 AND -DQB1; Low resolution human leukocyte antigen (HLA) Class II typing of HLA-DRB1/3/4/5 and HLA-DQB1
+3 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81376 |
HLA Class II typing, low resolution (eg, antigen equivalents); one locus (eg, HLA-DRB1, -DRB3/4/5, -DQB1, -DQA1, -DPB1, or -DPA1), each
HLA CLASS II TYPING LOW RESOLUTION ONE LOCUS EA; Low resolution human leukocyte antigen (HLA) Class II typing of HLA-DQA1
+6 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81377 |
HLA Class II typing, low resolution (eg, antigen equivalents); one antigen equivalent, each
HLA II LOW RESOLUTION ONE ANTIGEN EQUIVALENT EA; HLA class II typing low resolution one antigen equivalent
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81378 |
HLA Class I and II typing, high resolution (ie, alleles or allele groups), HLA-A, -B, -C, and -DRB1
High resolution human leukocyte antigen (HLA) Class I and II typing of HLA-A, HLA-B, HLA-C,and HLA-DRB1/3/4/5; HLA class I and II typing high resolution HLA-A, -B, -C, and -DRB1
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81379 |
HLA Class I typing, high resolution (ie, alleles or allele groups); complete (ie, HLA-A, -B, and -C)
Complete high resolution human leukocyte antigen (HLA) Class I typing; HLA Class I typing high resolution
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81380 |
HLA Class I typing, high resolution (ie, alleles or allele groups); one locus (eg, HLA-A, -B, or -C), each
High resolution human leukocyte antigen (HLA) Class I typing of locus; HLA CLASS I TYPING HIGH RESOLUTION ONE LOCUS EA
+4 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81381 |
HLA Class I typing, high resolution (ie, alleles or allele groups); one allele or allele group (eg, B*57:01P), each
High resolution human leukocyte antigen (HLA) Class I typing of allele group; High resolution human leukocyte antigen (HLA) Class I typing of allele
+3 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81382 |
HLA Class II typing, high resolution (ie, alleles or allele groups); one locus (eg, HLA-DRB1, -DRB3/4/5, -DQB1, -DQA1, -DPB1, or -DPA1), each
HLA class II typing high resolution one locus; High resolution human leukocyte antigen (HLA) Class II typing of HLA-DPA1
+9 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81383 |
HLA Class II typing, high resolution (ie, alleles or allele groups); one allele or allele group (eg, HLA-DQB1*06:02P), each
High resolution human lymphocyte antigen Class II typing of allele; High resolution human lymphocyte antigen Class II typing of HLA-DQB1*06:02P
+3 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81400 |
Molecular pathology procedure, Level 1
Coagulation factor V (F5) gene analysis for detection of HR2 variant using restriction enzyme digestion method; Chemokine C-C motif receptor 5 (CCR5) gene analysis for detection of 32-bp deletion mutation/794 825del32 deletion
+76 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81401 |
Molecular pathology procedure, Level 2
Mitochondrially encoded ATP synthase 6 (MT-ATP6) gene analysis for detection of m.8993T>G and m.8993T>C variants; EML4/ALK (inv(2)) inversion analysis
+201 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81402 |
Molecular pathology procedure, Level 3
Gene analysis for detection of T-cell receptor gene rearrangement; Chromosome 18q allelic imbalance assessment of microsatellite marker D18S69
+56 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81403 |
Molecular pathology procedure, Level 4
Myeloproliferative leukemia virus oncogene, thrombopoietin receptor, TPOR (MPL) targeted sequence analysis of exon 10; Ki-ras2 Kirsten rat sarcoma viral oncogene (KRAS) gene analysis for detection of codon 61 variant
+47 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81404 |
Molecular pathology procedure, Level 5
Facioscapulohumeral muscular dystrophy 1A (FSHMD1A) gene analysis for characterization of chromosome 4A haplotype; Ret proto-oncogene (RET) gene analysis for detection of 2647_2648delinsTT variant
+91 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81405 |
Molecular pathology procedure, Level 6
Actin, alpha, cardiac muscle 1 (ACTC1) full gene sequence analysis; Neurofilament, light polypeptide (NEFL) full gene sequence analysis
+76 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81406 |
Molecular pathology procedure, Level 7
Troponin T, type 2 [cardiac] (TNNT2) full gene sequence analysis; Lamin A/C (LMNA) full gene sequence analysis
+80 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81407 |
Molecular pathology procedure, Level 8
Myosin binding protein C, cardiac (MYBPC3) full gene sequence analysis; Level 8 molecular pathology gene analysis using mutation scanning method
+22 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81408 |
Molecular pathology procedure, Level 9
Ryanodine receptor 1, skeletal (RYR1) full gene sequence analysis; Molecular pathology procedure level 9
+12 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81410 |
Aortic dysfunction or dilation (eg, Marfan syndrome, Loeys Dietz syndrome, Ehler Danlos syndrome type IV, arterial tortuosity syndrome); genomic sequence analysis panel, must include sequencing of at least 9 genes, including FBN1, TGFBR1, TGFBR2, COL3A1, MYH11, ACTA2, SLC2A10, SMAD3, and MYLK
Aortic dilation gene deletion analysis for detection of FBN1, TGFBR1, TGFBR2, COL3A1, MYH11, ACTA2, SLC2A10, SMAD3, and MYLK variants; Aortic dysfunction gene deletion analysis for detection of FBN1, TGFBR1, TGFBR2, COL3A1, MYH11, ACTA2, SLC2A10, SMAD3, and MYLK variants
+4 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81411 |
Aortic dysfunction or dilation (eg, Marfan syndrome, Loeys Dietz syndrome, Ehler Danlos syndrome type IV, arterial tortuosity syndrome); duplication/deletion analysis panel, must include analyses for TGFBR1, TGFBR2, MYH11, and COL3A1
Aortic dilation gene duplication analysis for detection of TGFBR1, TGFBR2, MYH11, and COL3A1 variants; Aortic dysfunction gene deletion analysis for detection of TGFBR1, TGFBR2, MYH11, and COL3A1 variants
+4 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81412 |
Ashkenazi Jewish associated disorders (eg, Bloom syndrome, Canavan disease, cystic fibrosis, familial dysautonomia, Fanconi anemia group C, Gaucher disease, Tay-Sachs disease), genomic sequence analysis panel, must include sequencing of at least 9 genes, including ASPA, BLM, CFTR, FANCC, GBA, HEXA, IKBKAP, MCOLN1, and SMPD1
Test for detecting genes for disorders related to Ashkenazi Jews; ASHKENAZI JEWISH ASSOC DSRDRS GEN SEQ ANAL 9 GEN
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81413 |
Cardiac ion channelopathies (eg, Brugada syndrome, long QT syndrome, short QT syndrome, catecholaminergic polymorphic ventricular tachycardia); genomic sequence analysis panel, must include sequencing of at least 10 genes, including ANK2, CASQ2, CAV3, KCNE1, KCNE2, KCNH2, KCNJ2, KCNQ1, RYR2, and SCN5A
Cardiac ion channelopathies duplication/deletion gene analysis panel with sequencing of 10 or more genes, including ANK2, CASQ2, CAV3, KCNE1, KCNE2, KCNH2, KCNJ2, KCNQ1, RYR2, and SCN5A; Test for detecting genes associated with heart disease
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81414 |
Cardiac ion channelopathies (eg, Brugada syndrome, long QT syndrome, short QT syndrome, catecholaminergic polymorphic ventricular tachycardia); duplication/deletion gene analysis panel, must include analysis of at least 2 genes, including KCNH2 and KCNQ1
Cardiac ion channelopathies duplication/deletion gene analysis panel with analysis of at least genes, including KCNH2 and KCNQ1; CAR ION CHNNLPATH DUP/DEL GN ALYS PANEL 2 GENES
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81415 |
Exome (eg, unexplained constitutional or heritable disorder or syndrome); sequence analysis
Exome sequence analysis; EXOME SEQUENCE ANALYSIS
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81416 |
Exome (eg, unexplained constitutional or heritable disorder or syndrome); sequence analysis, each comparator exome (eg, parents, siblings) (List separately in addition to code for primary procedure)
Test for detecting genes associated with disease; EXOME SEQUENCE ANALYSIS EACH COMPARATOR EXOME
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81417 |
Exome (eg, unexplained constitutional or heritable disorder or syndrome); re-evaluation of previously obtained exome sequence (eg, updated knowledge or unrelated condition/syndrome)
EXOME RE-EVAL OF PREVIOUSLY OBTAINED EXOME SEQ; Exome sequence analysis
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81420 |
Fetal chromosomal aneuploidy (eg, trisomy 21, monosomy X) genomic sequence analysis panel, circulating cell-free fetal DNA in maternal blood, must include analysis of chromosomes 13, 18, and 21
Fetal chromosomal aneuploid genomic sequence analysis; Fetal chromosomal aneuploid genomic sequence analysis panel
+2 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81422 |
Fetal chromosomal microdeletion(s) genomic sequence analysis (eg, DiGeorge syndrome, Cri-du-chat syndrome), circulating cell-free fetal DNA in maternal blood
FETAL CHROMOSOMAL MICRODELTJ GENOMIC SEQ ANALYS; Fetal chromosomal microdeletion genomic sequence analysis of circulating cell-free fetal DNA in maternal blood
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81425 |
Genome (eg, unexplained constitutional or heritable disorder or syndrome); sequence analysis
Genome sequence analysis; Test for detecting genes associated with disease
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81426 |
Genome (eg, unexplained constitutional or heritable disorder or syndrome); sequence analysis, each comparator genome (eg, parents, siblings) (List separately in addition to code for primary procedure)
Genome sequence analysis; Test for detecting genes associated with disease
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81427 |
Genome (eg, unexplained constitutional or heritable disorder or syndrome); re-evaluation of previously obtained genome sequence (eg, updated knowledge or unrelated condition/syndrome)
GENOME RE-EVALUATION OF PREC OBTAINED GENOME SEQ; Genome sequence analysis
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81430 |
Hearing loss (eg, nonsyndromic hearing loss, Usher syndrome, Pendred syndrome); genomic sequence analysis panel, must include sequencing of at least 60 genes, including CDH23, CLRN1, GJB2, GPR98, MTRNR1, MYO7A, MYO15A, PCDH15, OTOF, SLC26A4, TMC1, TMPRSS3, USH1C, USH1G, USH2A, and WFS1
Test for detecting genes causing hearing loss; HEARING LOSS GENOMIC SEQUENCE ANALYSIS 60 GENES
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81431 |
Hearing loss (eg, nonsyndromic hearing loss, Usher syndrome, Pendred syndrome); duplication/deletion analysis panel, must include copy number analyses for STRC and DFNB1 deletions in GJB2 and GJB6 genes
HEARING LOSS DUP/DEL ANALYSIS; Test for detecting genes causing hearing loss
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81432 |
Hereditary breast cancer-related disorders (eg, hereditary breast cancer, hereditary ovarian cancer, hereditary endometrial cancer); genomic sequence analysis panel, must include sequencing of at least 10 genes, always including BRCA1, BRCA2, CDH1, MLH1, MSH2, MSH6, PALB2, PTEN, STK11, and TP53
HEREDITARY BRST CA-RELATED GEN SEQ ANALYS 10 GEN; Hereditary breast cancer related disorders genomic sequence analysis
+2 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81433 |
Hereditary breast cancer-related disorders (eg, hereditary breast cancer, hereditary ovarian cancer, hereditary endometrial cancer); duplication/deletion analysis panel, must include analyses for BRCA1, BRCA2, MLH1, MSH2, and STK11
HEREDITARY BRST CA-RELATED DUP/DEL ANALYSIS; Gene analysis (breast and related cancers), duplication or deletion variants
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81434 |
Hereditary retinal disorders (eg, retinitis pigmentosa, Leber congenital amaurosis, cone-rod dystrophy), genomic sequence analysis panel, must include sequencing of at least 15 genes, including ABCA4, CNGA1, CRB1, EYS, PDE6A, PDE6B, PRPF31, PRPH2, RDH12, RHO, RP1, RP2, RPE65, RPGR, and USH2A
HEREDITARY RETINAL DSRDRS GEN SEQ ANALYS 15 GEN; Gene analysis (retinal disorders), genomic sequence
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81435 |
Hereditary colon cancer disorders (eg, Lynch syndrome, PTEN hamartoma syndrome, Cowden syndrome, familial adenomatosis polyposis); genomic sequence analysis panel, must include sequencing of at least 10 genes, including APC, BMPR1A, CDH1, MLH1, MSH2, MSH6, MUTYH, PTEN, SMAD4, and STK11
HEREDITARY COLON CA DSRDRS GEN SEQ ANALYS 10 GEN; Test for detecting genes associated with colon cancer
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81436 |
Hereditary colon cancer disorders (eg, Lynch syndrome, PTEN hamartoma syndrome, Cowden syndrome, familial adenomatosis polyposis); duplication/deletion analysis panel, must include analysis of at least 5 genes, including MLH1, MSH2, EPCAM, SMAD4, and STK11
HEREDITARY COLON CA DSRDRS DUP/DEL ANALYS 5 GEN; Hereditary colon cancer syndrome gene analysis for detection of deletion and duplication variants including APC, MLH1, MSH2, MSH6, PMS2, EPCAM, CHEK2, and MUTYH genes
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81437 |
Hereditary neuroendocrine tumor disorders (eg, medullary thyroid carcinoma, parathyroid carcinoma, malignant pheochromocytoma or paraganglioma); genomic sequence analysis panel, must include sequencing of at least 6 genes, including MAX, SDHB, SDHC, SDHD, TMEM127, and VHL
Gene analysis (neuroendocrine tumors), genomic sequence; HEREDTRY NURONDCRN TUM DSRDRS GEN SEQ ANAL 6 GEN
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|
|
| 81438 |
Hereditary neuroendocrine tumor disorders (eg, medullary thyroid carcinoma, parathyroid carcinoma, malignant pheochromocytoma or paraganglioma); duplication/deletion analysis panel, must include analyses for SDHB, SDHC, SDHD, and VHL
HEREDTRY NURONDCRN TUM DSRDRS DUP/DEL ANALYSIS; Neuroendocrine tumor disorders (SDHB, SDHC, SDHD, VHL) gene analysis for detection of duplication and deletion variants
+1 more
|
Active |
http://purl.bioontology.org/ontology/STY/T059
|