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Disease Ontology Term: Lynch syndrome

DO ID
DOID:3883
Description
An autosomal dominant disease that is characterized by an increased risk for colon cancer and cancers of the endometrium, ovary, stomach, small intestine, hepatobiliary tract, urinary tract, brain, and skin and has_material_basis_in mutation of mismatch repair genes that increases the risk of many types of cancers.
Synonyms
Hereditary Defective Mismatch Repair syndrome, Hereditary non-polyposis colon cancer, Hereditary nonpolyposis colon cancer, Hereditary non-polyposis colon cancer syndrome, Hereditary nonpolyposis colon cancer syndrome, hereditary nonpolyposis colorectal cancer, Hereditary non-polyposis colorectal cancer, Hereditary non-polyposis colorectal cancer syndrome, Hereditary nonpolyposis colorectal cancer syndrome, hereditary nonpolyposis colorectal neoplasm, HNPCC
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High-throughput

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Computational

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Gene Disease Ontology Term Qualifier Evidence Method Source Assigned On Reference