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References OMIM Gene GeneReviews HGMD HGNC
GENATLAS PHENOTYPE
last update : 26/09/2007
Symbol WS2B
Location 1p13
HGNC id 12794
Name Waardenburg syndrome, type 2B
Main clinical features partial albinism, deafness, without dystopia canthorum
Genetic determination autosomal dominant
Function/system disorder ear
dermatology
Type disease
Remark(s) not confirmed