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| Term | Waardenburg syndrome type 2B | ID (Ontology) | DOID:0110947 (Human Disease) |
| Definition | A Waardenburg syndrome characterized by pigmentary abnormalities of the hair, skin, and eyes, congenital sensorineural hearing loss, and absence of lateral displacement of the inner canthus of each eye that has_material_basis_in variation in the chromosome region 1p21-p13.3. | ||
| Also Known As | "Waardenburg syndrome type IIB" ; "WS2B" | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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autosomal dominant disease__ syndrome____________________| Waardenburg syndrome |__Waardenburg syndrome type 2B |
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| Is a | Waardenburg syndrome | ||
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GARD:5522 MESH:C536465 MIM:600193 |
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