Universal Clinical Codes & Terminology Search

Suprachoroidal injection of a pharmacologic agent (does not include supply of medication)

Oncology (urothelial carcinoma) DNA quantitative methylation-specific PCR of 2 genes (ONECUT2 VIM) algorithmic analysis reported as positive or negative

Insertion of chest wall respiratory sensor electrode or electrode array including connection to pulse generator (List separately in addition to code for primary procedure)

Cardiology (coronary artery disease [CAD]) DNA genome-wide association studies (564856 single-nucleotide polymorphisms [SNPs] targeted variant genotyping) patient lifestyle and clinical data buccal swab algorithm reported as polygenic risk to acquired heart disease

Revision or replacement of chest wall respiratory sensor electrode or electrode array including connection to existing pulse generator

Oncology (bladder) DNA next-generation sequencing (NGS) of 60 genes and whole genome aneuploidy urine algorithms reported as minimal residual disease (MRD) status positive or negative and quantitative disease burden

Removal of chest wall respiratory sensor electrode or electrode array

Hepatology (nonalcoholic steatohepatitis [NASH]) miR-34a-5p alpha 2-macroglobulin YKL40 HbA1c serum and whole blood algorithm reported as a single score for NASH activity and fibrosis

Retinal polarization scan ocular screening with on-site automated results bilateral

Rare diseases (constitutional/heritable disorders) whole genome sequence analysis for chromosomal abnormalities copy number variants duplications/deletions inversions unbalanced translocations regions of homozygosity (ROH) inheritance pattern that indicate uniparental disomy (UPD) and aneuploidy fetal sample (amniotic fluid chorionic villus sample or products of conception) identification and categorization of genetic variants diagnostic report of fetal results based on phenotype with maternal s

Optical coherence tomography (OCT) for microstructural and morphological imaging of skin image acquisition interpretation and report; first lesion

Oncology (oropharyngeal) detection of minimal residual disease by next-generation sequencing (NGS) based quantitative evaluation of 8 DNA targets cell-free HPV 16 and 18 DNA from plasma

Optical coherence tomography (OCT) for microstructural and morphological imaging of skin image acquisition interpretation and report; each additional lesion (List separately in addition to code for primary procedure)

Oncology (colorectal cancer) qualitative real-time PCR of 35 variants of KRAS and NRAS genes (exons 2 3 4) formalin-fixed paraffin-embedded (FFPE) predictive identification of detected mutations

Device evaluation interrogation and initial programming of intraocular retinal electrode array (eg retinal prosthesis) in person with iterative adjustment of the implantable device to test functionality select optimal permanent programmed values with analysis including visual training with review and report by a qualified health care professional

Carbonic anhydrase VI (CA VI) parotid specific/secretory protein (PSP) and salivary protein (SP1) IgG IgM and IgA antibodies enzyme-linked immunosorbent assay (ELISA) semiqualitative blood reported as predictive evidence of early Sjogren syndrome

Device evaluation and interrogation of intraocular retinal electrode array (eg retinal prosthesis) in person including reprogramming and visual training when performed with review and report by a qualified health care professional

Oncology (solid tumor) next-generation sequencing (NGS) of DNA from formalin-fixed paraffin-embedded (FFPE) tissue with comparative sequence analysis from a matched normal specimen (blood or saliva) 648 genes interrogation for sequence variants insertion and deletion alterations copy number variants rearrangements microsatellite instability and tumor-mutation burden

Insertion of anterior segment aqueous drainage device with creation of intraocular reservoir internal approach into the supraciliary space

Hereditary pan-cancer (eg hereditary sarcomas hereditary endocrine tumors hereditary neuroendocrine tumors hereditary cutaneous melanoma) genomic sequence analysis panel of 88 genes with 20 duplications/deletions using next-generation sequencing (NGS) Sanger sequencing blood or saliva reported as positive or negative for germline variants each gene