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S3844 Dna analysis of the connexin 26 gene (gjb2) for susceptibility to congenital, profound deafness
BackS3000Diabetic indicator; retinal eye exam, dilated, bilateral→S3005Performance measurement, evaluation of patient self assessment, depression→S3600Stat laboratory request (situations other than s3601)→S3601Emergency stat laboratory charge for patient who is homebound or residing in a nursing facility→S3620Newborn metabolic screening panel, includes test kit, postage and the laboratory tests specified by the state for inclusion in this panel (e.g., galactose; hemoglobin, electrophoresis; hydroxyprogesterone, 17-d; phenylalanine (pku); and thyroxine, total)→S3630Eosinophil count, blood, direct→S3645Hiv-1 antibody testing of oral mucosal transudate→S3650Saliva test, hormone level; during menopause→S3652Saliva test, hormone level; to assess preterm labor risk→S3655Antisperm antibodies test (immunobead)→S3708Gastrointestinal fat absorption study→S3722Dose optimization by area under the curve (auc) analysis, for infusional 5-fluorouracil→S3800Genetic testing for amyotrophic lateral sclerosis (als)→S3840Dna analysis for germline mutations of the ret proto-oncogene for susceptibility to multiple endocrine neoplasia type 2→S3841Genetic testing for retinoblastoma→S3842Genetic testing for von hippel-lindau disease→S3844Dna analysis of the connexin 26 gene (gjb2) for susceptibility to congenital, profound deafness→S3845Genetic testing for alpha-thalassemia→S3846Genetic testing for hemoglobin e beta-thalassemia→S3849Genetic testing for niemann-pick disease→S3850Genetic testing for sickle cell anemia→S3852Dna analysis for apoe epsilon 4 allele for susceptibility to alzheimer's disease→S3853Genetic testing for myotonic muscular dystrophy→S3854Gene expression profiling panel for use in the management of breast cancer treatment→S3861Genetic testing, sodium channel, voltage-gated, type v, alpha subunit (scn5a) and variants for suspected brugada syndrome→S3865Comprehensive gene sequence analysis for hypertrophic cardiomyopathy→S3866Genetic analysis for a specific gene mutation for hypertrophic cardiomyopathy (hcm) in an individual with a known hcm mutation in the family→S3870Comparative genomic hybridization (cgh) microarray testing for developmental delay, autism spectrum disorder and/or intellectual disability→S3900Surface electromyography (emg)→S3902Ballistocardiogram→S3904Masters two step→
Procedure codeCODABLE
S3844
Dna analysis of the connexin 26 gene (gjb2) for susceptibility to congenital, profound deafness
- Part
- HCPCS Level II
- S
- Temporary National Codes (Non-Medicare)
- S3
- S3000–S3904
Source
CMS — ICD-10-PCS FY2026, HCPCS Level II october 2026, Procedure Codes 2026.