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HCPCS Codes Lookup
M1412 | Similar
HCPCS Codes Similar to M1412
HCPCS Codes Similar to “M1412” Code.
Patients with metastatic nsclc with epidermal growth factor receptor (egfr) mutations, alk genomic tumor aberrations, or other targetable genomic abnormalities with approved first-line targeted therapy, such as nsclc with ros1 rearrangement, braf v600e mutation, ntrk 1/2/3 gene fusion, met ex14 skipping mutation, and ret rearrangement
A6025
Gel sheet for dermal or epidermal application, (e.g., silicone, hydrogel, other), each
Code added date
: 19970101
Code effective date
: 20070101
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S3870
Comparative genomic hybridization (cgh) microarray testing for developmental delay, autism spectrum disorder and/or intellectual disability
Code added date
: 20090401
Code effective date
: 20140101
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S3840
Dna analysis for germline mutations of the ret proto-oncogene for susceptibility to multiple endocrine neoplasia type 2
Code added date
: 20030701
Code effective date
: 20030701
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S3855
Genetic testing for detection of mutations in the presenilin - 1 gene
Code added date
: 20070101
Code effective date
: 20150101
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S9055
Procuren or other growth factor preparation to promote wound healing
Code added date
: 20000101
Code effective date
: 20000101
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S9558
Home injectable therapy; growth hormone, including administrative services, professional pharmacy services, care coordination, and all necessary supplies and equipment (drugs and nursing visits coded separately), per diem
Code added date
: 20020101
Code effective date
: 20020101
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G9840
Ras (kras and nras) gene mutation testing performed before initiation of anti-egfr moab
Code added date
: 20170101
Code effective date
: 20180101
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G9841
Ras (kras and nras) gene mutation testing not performed before initiation of anti-egfr moab
Code added date
: 20170101
Code effective date
: 20180101
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G9834
Patient has metastatic disease at diagnosis
Code added date
: 20170101
Code effective date
: 20210101
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G9838
Patient has metastatic disease at diagnosis
Code added date
: 20170101
Code effective date
: 20170101
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G9842
Patient has metastatic disease at diagnosis
Code added date
: 20170101
Code effective date
: 20170101
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G9843
Ras (kras or nras) gene mutation
Code added date
: 20170101
Code effective date
: 20180101
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S3831
Single-mutation analysis (in individual with a known mlh1 and msh2 mutation in the family) for hereditary nonpolyposis colorectal cancer (hnpcc) genetic testing
Code added date
: 20020101
Code effective date
: 20120401
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S3866
Genetic analysis for a specific gene mutation for hypertrophic cardiomyopathy (hcm) in an individual with a known hcm mutation in the family
Code added date
: 20090401
Code effective date
: 20090401
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