Waardenburg Syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D014849
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1 genes/proteins associated with the disease Waardenburg Syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
PAX3 paired box 3 2.88009