DISEASES

Disease-gene associations mined from literature

SearchDownloadsAbout

Human genes for syndactyly type 1

Syndactyly type 1 [DOID:0111816]

A syndactyly characterized by complete or partial webbing between the third and fourth fingers and/or the second and third toes that has_material_basis_in heterozygous duplication of a region of chromosome 2q34-q36.

Synonyms:  syndactyly type 1,  DOID:0111816,  chromosome 2q35 duplication syndrome,  SDTY1,  syndactyly, type 1, with or without craniosynostosis ...

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.