DISEASES

Disease-gene associations mined from literature

Human genes for Waardenburg's syndrome

Waardenburg's syndrome [DOID:9258]

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.

Synonyms:  Waardenburg's syndrome,  DOID:9258,  Waardenburgs syndrome,  Waardenburg's disease,  Waardenburg's disorder ...

Linkouts:  OMIM #1 #2 #3 #4 #5 #6 #7 #8 #9 #10