DISEASES

Disease-gene associations mined from literature

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Human genes for Treacher Collins syndrome

Treacher Collins syndrome [DOID:2908]

A syndrome that is characterized by bilateral and symmetric downslanting palpebral fissures, malar hypoplasia, micrognathia, and external ear abnormalities.

Synonyms:  Treacher Collins syndrome,  DOID:2908,  Treacher Collins disease,  Treacher Collins disorder,  Treacher Collins syndromes ...

Linkouts:  OMIM #1 #2 #3 #4 #5 #6

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.