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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's 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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last database update
11/30/2021
MGI 6.17
The Jackson Laboratory