Disease_Mapped_To_Gene Cellosaurus Disease Terminology PAX3 Gene Waardenburg Syndrome Type 1 C1847800 Waardenburg_Syndrome_Type_1 C75008 A rare autosomal dominant syndrome caused by mutations in the PAX3 gene. It is characterized by hearing loss, dystopia canthorum (widely spaced inner corners of the eyes), and changes in the color of the skin, hair, and eyes. Waardenburg Syndrome Type 1 Cellosaurus Waardenburg Syndrome Type I Waardenburg Syndrome Type 1 Disease or Syndrome Waardenburg Syndrome