S3842 Genetic testing for von hippel-lindau disease billable
S3844 Dna analysis of the connexin 26 gene (gjb2) for susceptibility to congenital, profound deafness billable
S3845 Genetic testing for alpha-thalassemia billable
S3846 Genetic testing for hemoglobin e beta-thalassemia billable
S3849 Genetic testing for niemann-pick disease billable
S3850 Genetic testing for sickle cell anemia billable
S3852 Dna analysis for apoe epsilon 4 allele for susceptibility to alzheimer's disease billable
S3853 Genetic testing for myotonic muscular dystrophy billable
S3854 Gene expression profiling panel for use in the management of breast cancer treatment billable
S3861 Genetic testing, sodium channel, voltage-gated, type v, alpha subunit (scn5a) and variants for suspected brugada syndrome billable
S3865 Comprehensive gene sequence analysis for hypertrophic cardiomyopathy billable
S3866 Genetic analysis for a specific gene mutation for hypertrophic cardiomyopathy (hcm) in an individual with a known hcm mutation in the family billable