DISEASES

Disease-gene associations mined from literature

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Human genes for distal arthrogryposis type 1

Distal arthrogryposis type 1 [DOID:0111596]

A distal arthrogryposis characterized by autosomal domiant inheritance of contractures of the distal regions of the hands and feet with no facial involvement or other anomalies.

Synonyms:  distal arthrogryposis type 1,  DOID:0111596,  DA1,  digitotalar dysmorphism,  digitotalar dysmorphisms

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.