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| 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 |