Diseases title

Waardenburg syndrome )

Chromosomes2
Orpha Number: 3440
Synonym(s):

Waardenburg syndrome (WS) is an autosomal dominant disorder characterized by varying degrees of deafness, minor defects in structures arising from neural crest and pigmentation anomalies of eyes, hair, and skin. WS is classified into four clinical and genetic phenotypes.
source: Orphanet