Lynch Syndrome 1
Disease ID: disease_node_17095
Connections displayed (default: 10).
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| Dbxref | MIM:120435, NCI:C6725, UMLS_CUI:C2936783 |
|---|---|
| Subclassof | DOID_3883 |
| Data Source | DOID |
| Synonyms | COCA1, FCC1, HNPCC1, familial nonpolyposis colon cancer type 1, hereditary nonpolyposis colorectal cancer type 1 |
| Doid Label | Lynch syndrome 1 |
| Doid Description | A Lynch syndrome that has_material_basis_in heterozygous mutations in the MSH2 gene on chromosome 2p21-p16. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_17095 |
| Doid Id | DOID_0070271 |
| Label | Lynch Syndrome 1 |
- Outgoing r'ship
SUBCLASS_OFto/from Colorectal Neoplasms, Hereditary Nonpolyposis(ID:disease_node_2182) (Disease)