Waardenburg Syndrome OMIM# PS193500

Facial Gestalt

Visualization generated by Face2Gene.


Associated Genes


• WS2B; WS2C

• SNAI2; SOX10



see more >


Key Features

  • hearing impairment
  • white forelock
  • hypertelorism
  • smooth philtrum
  • heterochromia iridis

London Medical Databases:
Waardenburg Syndrome
OMIM# PS193500


Born out of decades of research and data collection, London Medical Databases (LMD) is the most comprehensive resource for photos and information about syndromes, genes and clinical phenotypes.

Log in to LMD to access this content.