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Disease Ontology Browser
Waardenburg syndrome type 3 (DOID:0110949)
Alliance: disease page
Synonyms: Klein-Waardenburg syndrome; Waardenburg syndrome type III; Waardenburg syndrome with upper limb anomalies; WS3
Alt IDs: OMIM:148820, ICD10CM:E70.3, ORDO:896
Definition: A Waardenburg syndrome characterized by upper limb anomalies, congenital hearing loss, dystopia canthorum and pigmentation anomalies of eyes, hair, and skin that has_material_basis_in heterozygous or homozygous mutation in the PAX3 gene on chromosome 2q36.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
04/09/2024
MGI 6.23 		The Jackson Laboratory