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HCPCS Procedure & Supply Codes

-/+ Deleted, Replaced, Expanded Codes

section notes

S0000-S9999 -/+ Deleted, Replaced, Expanded Codes

section notes

S3000-S3999 -/+ Deleted, Replaced, Expanded Codes

section notes
S3618   BLOOD CHEMISTRY FOR FREE BETA HUMAN CHORIONIC GONADOTROPIN (HCG)
S3625   Maternal serum triple marker screen including alpha-fetoprotein (afp), estriol, ...
S3626   Maternal serum quadruple marker screen including alpha-fetoprotein (afp), estrio...
S3628   Placental alpha microglobulin-1 rapid immunoassay for detection of rupture of fe...
S3701   IMMUNOASSAY FOR NUCLEAR MATRIX PROTEIN 22 (NMP-22), QUANTITATIVE
S3711   Circulating tumor cell test
S3713   Kras mutation analysis testing
S3818   Complete gene sequence analysis; brca1 gene
S3819   Complete gene sequence analysis; brca2 gene
S3820   Complete brca1 and brca2 gene sequence analysis for susceptibility to breast and...
S3822   Single mutation analysis (in individual with a known brca1 or brca2 mutation in ...
S3823   Three-mutation brca1 and brca2 analysis for susceptibility to breast and ovarian...
S3828   Complete gene sequence analysis; mlh1 gene
S3829   Complete gene sequence analysis; msh2 gene
S3830   Complete mlh1 and msh2 gene sequence analysis for hereditary nonpolyposis colore...
S3831   Single-mutation analysis (in individual with a known mlh1 and msh2 mutation in t...
S3833   Complete apc gene sequence analysis for susceptibility to familial adenomatous p...
S3834   Single-mutation analysis (in individual with a known apc mutation in the family)...
S3835   Complete gene sequence analysis for cystic fibrosis genetic testing
S3837   Complete gene sequence analysis for hemochromatosis genetic testing
S3843   Dna analysis of the f5 gene for susceptibility to factor v leiden thrombophilia
S3847   Genetic testing for tay-sachs disease
S3848   Genetic testing for gaucher disease
S3851   Genetic testing for canavan disease
S3855   Genetic testing for detection of mutations in the presenilin - 1 gene
S3860   Genetic testing, comprehensive cardiac ion channel analysis, for variants in 5 m...
S3862   Genetic testing, family-specific ion channel analysis, for blood-relatives of in...
S3905   Non-invasive electrodiagnostic testing with automatic computerized hand-held dev...
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