Lynch syndrome 1
Information
- Disease name
- Lynch syndrome 1
- Disease ID
- DOID:0070271
- Description
- "A Lynch syndrome that has_material_basis_in heterozygous mutations in the MSH2 gene on chromosome 2p21-p16." [url:https\://www.ncbi.nlm.nih.gov/pubmed/8261515, url:https\://www.ncbi.nlm.nih.gov/pubmed/8574961]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
- Disase is a (Disease Ontology)
- DOID:3883
- Cross Reference ID (Disease Ontology)
- MIM:120435
- Exact Synonym (Disease Ontology)
- familial nonpolyposis colon cancer type 1
- Exact Synonym (Disease Ontology)
- FCC1
- Exact Synonym (Disease Ontology)
- hereditary nonpolyposis colorectal cancer type 1
- Exact Synonym (Disease Ontology)
- HNPCC1