HCPCS Level II
S3865
Comprehensive gene sequence analysis for hypertrophic cardiomyopathy
- Category
- S. Temporary national codes
- NDC crosswalk
- None in the loaded CMS ASP file
Codes near S3865
These sit next to S3865 in the CMS Level II file. All S codes
- 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
- S3855Genetic testing for detection of mutations in the presenilin - 1 gene
- S3861Genetic testing, sodium channel, voltage-gated, type v, alpha subunit (scn5a) and variants for suspected brugada syndrome
- 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
- S3890Dna analysis, fecal, for colorectal cancer screening
- S3900Surface electromyography (emg)
- S3902Ballistocardiogram