DISEASES

Disease-gene associations mined from literature

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Human genes for Waardenburg syndrome

Waardenburg syndrome [DOID:9258]

A syndrome characterized by varying degrees of deafness, minor defects in structures arising from the neural crest and pigmentation anomalies of the hair, the skin and/or the iris of both eyes.

Synonyms:  Waardenburg syndrome,  DOID:9258,  Waardenburg disease,  Waardenburg disorder,  Waardenburg syndromes ...

Linkouts:  OMIM #1 #2 #3 #4 #5 #6 #7 #8 #9 #10

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.

Currently maintained by Qingyao Huang at Swiss Institute of Bioinformatics, University of Zurich. Licensed under CC BY 4.0.