For your convenience, we’ve provided below a list of the CPT and ICD-10 codes for the clinical and laboratory services offered at Insight Medical Genetics.
Cancer (most common tests are listed below, more available)
| GENE/DISORDER | CODE(S) |
|---|---|
| BRCA 1/2 Sequencing and Del/Dup | 81162 |
| BRCA 1/2 Ashkenazi Target | 81212 |
| Lynch Syndrome | 81292 81295 81298 81294 81297 81300 81403 81317 81319 |
Consultation
| SERVICE | CODE(S) |
|---|---|
| MD and Genetic Counselor | 99243 or 99244 or 99245 |
| Genetic Counseling Only | S0265 |
First Trimester Screening
| SERVICE | CODE(S) |
|---|---|
| Cell-free DNA (NIPT) | 81425 81507 |
| Cell-free DNA (NIPT)(Blood Draw and Ultrasound) with Counseling | 81425 81507 36415 76801 76813 S0265 or 99243 |
| First Trimester Screening (Blood and Ultrasound) with Counseling | 81512 36415 76801 76813 S0265 or 99243 |
| First Trimester Screening (blood draw only) | 81512 |
| Ultrasound(s) | 76801 76813 (add 76802 and 76814 for twins) |
NextGen Panel Testing
| DISORDER | CODE(S) |
|---|---|
| Noonan Panel | 81442 |
| Noonan Panel - Targeted | 81406 |
| Osteogenesis Imperfecta/Skeletal Dysplasia Panel | 81404(x2) 81405(x2) 81406(x2) 81408(x2) |
| Osteogenesis Imperfecta - Targeted | 81406 |
Single Gene/Carrier Screening
| GENE/DISORDER | CODE(S) |
|---|---|
| ACADM | 81406 |
| Beta Thalassemia and other beta- globinopathies | 81364 81363 |
| Canavan Disease | 81406 |
| CFTR Del/Dup | 81223 81400 81401 |
| Cystic Fibrosis Sequencing | 81223 81224 |
| Congenital Disorder of Glycosylation Type 1A | 81406 |
| CPT II Deficiency | 81404 |
| Familial Mediterranean Fever | 81404 |
| Fragile X | 81244 |
| Fundamental Panel (CF, SMA, Fragile X Only) | 81223 81400 81401 81257 81259 81363 81364 |
| Gaucher Disease Sequencing (GBA Gene Sequencing) | 81261 |
| GJB2 and GJB6 | 81252 81254 |
| Glycogen Storage Disease Type 1A | 81404 |
| Hereditary Fructosuria - ALDO B | 81406 |
| Hex A Tay-Sachs | 81406 |
| IMG Extended Carrier Screening (Includes SMA-GT, FX, GJB6, GBA) | 81223 81364 81243 81401 81404 81405 81406 81407 81408 |
| Miscellaneous genetic testing | 81479 |
| Pompe disease | 81406 |
| SCAD: Short Chain acyl-CoA dehydrogenase deficiency | 81405 |
| SMA - Deletion and Genotyping (IMG) | 81400 81401 |
| SMA Genotyping | 81401 |
| Smith Lemli Opitz - DHCR7 | 81405 |
| Spinal Muscular Atrophy (SMN 1) | 81405 |
| Targeted Sequencing | 81403 |
| Tay-Sachs Enzyme Testing | 81406 |
Other Testing
| SERVICE | CODE(S) |
|---|---|
| Amniocentesis specimen testing (Does not include Microarray) | 88267 88235(x2) 88280 88291 82106 88377(x2) |
| Blood Draw | 36415 |
| CVS specimen testing (Does not include Microarray | 88267 88235(x2) 88280 88291 82106 88377(x2) 81265 |
| Fluorescence In-Situ Hybridization (FISH) Only | 88291 88273 88368 88369 |
| Karyotyping | 88230(x2) 88262 88291 |
| Maternal Cell Contamination Studies (MCC) | 81265 81266 (for multiples) |
| Microarray and MCC | 81229 81265 81266 (for multiples) |
| Microarray - fetal sample | 81229 81265 |
| POC-1 | 88230(x2) 88267 88280 88285 88291 88381 |