林奇综合征（Lynch syndrome）是一种因基因突变引起的显性遗传性癌症综合征。[1]发病部位主要位于右半结肠[2]。林奇综合征患者患大肠癌的概率为10%至80%。[3]
| 林奇综合征 | |
|---|---|
 | |
| 分类和外部资源 | |
| 医学专科 | 肿瘤学 |
| ICD-10 | C18、C20 |
| OMIM | 120435 |
| DiseasesDB | 5812 |
| Orphanet | 144、144、443909 |
参考文献
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