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Disease Ontology Browser
Waardenburg syndrome type 2B (DOID:0110947)
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Synonyms: Waardenburg syndrome type IIB; WS2B
Alt IDs: OMIM:600193
Definition: A Waardenburg's 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.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.12
The Jackson Laboratory