top of page
CPT CODE | PROCEDURE | PRICE |
|---|---|---|
0 | CT LIVER PELVIS w/ & w/o contrast, | 0 |
0 | CT UROGRAM w/ & w/o contrast | 0 |
73700 | CT LOWER EXTREMITY w/o contrast | 0 |
73701 | CT LOWER EXTREMITY w/ contrast | 0 |
73702 | CT LOWER EXTREMITY w/ & w/o contrast | 0 |
72131 | CT LUMBAR SPINE w/o contrast | 0 |
72132 | CT LUMBAR SPINE w/ contrast | 0 |
G0297 | CT LUNG SCREENING w/o contrast | 0 |
70486 | CT MAXILLOFACIAL w/o contrast | 0 |
70490 | CT NECK SOFT TISSUE w/o contrast | 0 |
TEST ID | Test Name | CPT Code |
|---|---|---|
FUROC | UroVysion for Detection of Bladder Cancer, Urine | 88120 |
ATHAL | Alpha-Globin Gene Analysis, Varies | 81269
88235-Tissue culture for amniotic fluid (if appropriate)
88240-Cryopreservation (if appropriate)
81265-Comparative analysis using Short Tandem Repeat (STR) markers; patient and comparative specimen (eg, pre-transplant recipient and donor germline testing, post-transplant non-hematopoietic recipient germline [eg, buccal swab or other germline tissue sample] and donor testing, twin zygosity testing or maternal cell contamination of fetal cells (if appropriate) |
APOEG | Apolipoprotein E Genotyping, Blood | 81401-APOE (apolipoprotein E) (eg, hyperlipoproteinemia type III, cardiovascular disease, Alzheimer disease), common variants (eg, *2, *3, *4) |
BTDZ | Biotinidase Deficiency, BTD Full Gene Analysis, Varies | 81404-BTD (biotinidase) (eg, biotinidase deficiency), full gene sequence |
BWRS | Beckwith-Wiedemann Syndrome/Russell-Silver Syndrome, Molecular Analysis, Varies | 81401-H19 (imprinted maternally expressed transcript [non-protein coding]) (eg, Beckwith-Wiedemann syndrome), methylation analysis
81401-KCNQ1OT1 (KCNQ1 overlapping transcript 1 [non-protein coding]) (eg, Beckwith-Wiedemann syndrome) methylation analysis
88233-Tissue culture, skin or solid tissue biopsy (if appropriate)
88240-Cryopreservation (if appropriate)
88235-Tissue culture for amniotic fluid (if appropriate)
81265-Comparative analysis using Short Tandem Repeat (STR) markers; patient and comparative specimen (eg, pre-transplant recipient and donor germline testing, post-transplant non-hematopoietic recipient germline [eg, buccal swab or other germline tissue sample] and donor testing, twin zygosity testing or maternal cell contamination of fetal cells (if appropriate) |
C9ORF | C9orf72 Hexanucleotide Repeat, Molecular Analysis, Varies | 81479
|
CDKZ | CDKN1C Gene, Full Gene Analysis, Varies | 81479
88233-Tissue culture, skin or solid tissue biopsy (if appropriate)
88240-Cryopreservation (if appropriate)
88235-Amniotic fluid culture (if appropriate)
81265-Maternal cell contamination (if appropriate) |
DRPL | Dentatorubral-Pallidoluysian Atrophy (DRPLA) Gene Analysis, Varies | 81177-ATN1 (ataxin 2) (eg, denatatorubral-pallidolyuysian atrophy) gene analysis, evaluation to detect abnormal (eg, expanded) alleles |
FABRZ | Fabry Disease, Full Gene Analysis, Varies | 81405-GLA (galactosidase, alpha) (eg, Fabry disease), full gene sequence |
FUFXS | Fragile X, Follow-up Analysis | 81244 |
FXS | Fragile X Syndrome, Molecular Analysis, Varies | 81243
88233 (if appropriate)
88240 (if appropriate)
88235 (if appropriate)
81265 (if appropriate)
81244 (if appropriate) |
GAAZ | Pompe Disease, Full Gene Analysis, Varies | 81406-GAA (glucosidase, alpha; acid) (eg, glycogen storage disease type II [Pompe disease]), full gene sequence
88233-Tissue culture, skin or solid tissue biopsy (if appropriate)
88240-Cryopreservation (if appropriate) |
bottom of page