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Disease Ontology Browser
Waardenburg syndrome type 4A (DOID:0110953)
Alliance: disease page
Synonyms: Waardenburg syndrome type IVA; Waardenburg syndrome with Hirschsprung disease type 4A; WS4A
Alt IDs: OMIM:277580
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 or homozygous mutation in the EDNRB gene on chromosome 13q22.

Disease References using Mouse Models (2)

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
07/05/2024
MGI 6.24
The Jackson Laboratory