|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An autosomal disease 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. (Human Disease Ontology, DOID_9258)|
|Downloads & Tools|
1 genes/proteins associated with the disease Waardenburg Syndrome from the curated CTD Gene-Disease Associations dataset.
|PAX3||paired box 3||2.88009|