DISEASES

Disease-gene associations mined from literature

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Human genes for brachydactyly-syndactyly syndrome

Brachydactyly-syndactyly syndrome [DOID:0050689]

A syndrome that is characterized by brachydactyly and syndactyly, has_material_basis_in heterozygous mutation in the HOXD13 gene on chromosome 2q31.

Synonyms:  brachydactyly-syndactyly syndrome,  brachydactylysyndactyly syndrome,  brachydactyly-syndactyly disease,  brachydactyly-syndactyly disorder,  brachydactyly-syndactyly syndromes ...

Linkouts:  OMIM

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.