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