Lynch syndrome 1 Disease Ontology Browser

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Disease Ontology Browser

Lynch syndrome 1 (DOID:0070271)
Alliance: disease page
Synonyms: familial nonpolyposis colon cancer type 1; FCC1; hereditary nonpolyposis colorectal cancer type 1; HNPCC1
Alt IDs: OMIM:120435
Definition: A Lynch syndrome that has_material_basis_in heterozygous mutations in the MSH2 gene on chromosome 2p21-p16.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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