| 검사코드 | 검사명 | 약어명 | 검사분류 | 보험코드 | 보험수가 |
|---|---|---|---|---|---|
| 4851 | SBMA(spinobulbar muscular atrophy) | SBMA(spinobulbar muscular atrophy) | 기타 | C5803016Z | 117,860 |
| 4852 | UGT1A1 genotype, Major variants (Irinotecan sensitivity) [Sequencing] | UGT1A1 genotype, Major variants (Irinotecan sensitivity) [Sequencing] | 기타-GFR | C5806366Z | 184,270 |
| 4853 | Avellino corneal dystrophy | Avellino corneal dystrophy | 기타 | C5801096Z | 66,980 |
| 4855 | NOTCH3 gene, Familial mutation (CADASIL) [Sequencing] | NOTCH3 gene, Familial mutation (CADASIL) [Sequencing] | 기타-GFR | C5805006Z | 184,270 |
| 4856 | Y chromosome microdeletions | Y chromosome microdeletions | 기타-GFR | 83,200 | |
| 4864 | DMPK gene [PCR & fragment analysis] | DMPK gene [PCR & fragment analysis] | 기타 | C5803116Z | 117,860 |
| 4866 | Factor V Leiden R534Q mutation | Factor V Leiden R534Q mutation | 기타 | C5801056Z | 66,980 |
| 4867 | Prothrombin G20210A mutation | Prothrombin G20210A mutation | 기타 | C5801046Z | 66,980 |
| 4868 | APC gene mutation | APC gene mutation | 기타 | C5809026Z | 670,920 |
| 4869 | MUTYH gene mutation | MUTYH gene mutation | 기타 | C5808766Z | 428,780 |
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