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Disease Ontology Browser
Waardenburg syndrome type 4C (DOID:0110955)
Alliance: disease page
Synonyms: Waardenburg syndrome type IVC; Waardenburg syndrome with Hirschsprung disease type 4C; WS4C
Alt IDs: OMIM:613266
Definition: A Waardenburg syndrome characterized by pigmentary abnormalities of the hair, skin, and eyes, congenital sensorineural hearing loss, and Hirschsprung disease that has_material_basis_in heterozygous mutation in the SOX10 gene on chromosome 22q13.

Disease References using Mouse Models (1)
Contributing Projects:
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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11/05/2024
MGI 6.24 		The Jackson Laboratory