DISEASES

Disease-gene associations mined from literature

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Human genes for Lynch syndrome 1

Lynch syndrome 1 [DOID:0070271]

A Lynch syndrome that has_material_basis_in heterozygous mutations in the MSH2 gene on chromosome 2p21-p16.

Synonyms:  Lynch syndrome 1,  DOID:0070271,  familial nonpolyposis colon cancer type 1,  FCC1,  hereditary nonpolyposis colorectal cancer type 1 ...

The disease-gene associations are derived from automatic text mining of the biomedical literature, manually curated database annotations, cancer mutation data, and genome-wide association studies. The confidence of each association is signified by stars, where ★★★★★ is the highest confidence and ★☆☆☆☆ is the lowest.

Developed by Sune Frankild, Alexander Junge, Albert Pallejà, Dhouha Grissa, Kalliopi Tsafou, and Lars Juhl Jensen from the Novo Nordisk Foundation Center for Protein Research.