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