DISEASES

Disease-gene associations mined from literature

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Human genes for branchiooculofacial syndrome

Branchiooculofacial syndrome [DOID:0050691]

A syndrome that is characterized by low birth weight and growth retardation, bilateral branchial clefts.

Synonyms:  branchiooculofacial syndrome,  DOID:0050691,  branchiooculofacial disease,  branchiooculofacial disorder,  branchiooculofacial 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.