DISEASES

Disease-gene associations mined from literature

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Human genes for syndactyly type 3

Syndactyly type 3 [DOID:0111817]

A syndactyly characterized by complete and bilateral syndactyly between the 4th and 5th fingers that has_material_basis_in heterozygous mutation in GJA1 on chromosome 6q22.31.

Synonyms:  syndactyly type 3,  DOID:0111817,  ringand little finger syndactyly,  SDTY3,  syndactyly of fingers 4 and 5 ...

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.