Lynch syndrome 1 (Q60195130)
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Lynch syndrome that has material basis in heterozygous mutations in the MSH2 gene on chromosome 2p21-p16
- familial nonpolyposis colon cancer type 1
- FCC1
- hereditary nonpolyposis colorectal cancer type 1
- HNPCC1
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Lynch syndrome 1 |
Lynch syndrome that has material basis in heterozygous mutations in the MSH2 gene on chromosome 2p21-p16 |
|
Statements
1 reference
Identifiers
1 reference
1 reference