DISEASES

Disease-gene associations mined from literature

SearchDownloadsAbout

Human genes for Goldenhar syndrome

Goldenhar syndrome [DOID:2907]

A syndrome that is characterized by incomplete development of the ear, nose, soft palate, lip, and mandible. It is associated with anomalous development of the first branchial arch and second branchial arch.

Synonyms:  Goldenhar syndrome,  DOID:2907,  Goldenhar disease,  Goldenhar disorder,  Goldenhar 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.