Disease-gene associations mined from literature

Human genes for Waardenburg's syndrome

Waardenburg's syndrome [DOID:9258]

Waardenburg syndrome (also Waardenburg­ Shah Syndrome, Waardenburg-Klein syndrome, Mende's syndrome II, Van der Hoeve-Halbertsma-Waardenburg syndrome, Ptosis-Epicanthus syndrome, Van der Hoeve-Halbertsma-Gualdi syndrome, Waardenburg type Pierpont, Van der Hoeve-Waardenburg-Klein syndrome, Waardenburg's syndrome II and Vogt’s syndrome.) is a rare genetic disorder most often characterized by varying degrees of deafness, minor defects in structures arising from the neural crest, and pigmentation anomalies.

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