About   Help   FAQ
Disease Ontology Browser
Waardenburg syndrome (DOID:9258)
Alliance: disease page
Synonyms: van der Hoeve Halbertsona Waardenburg syndrome; Waardenburg Shah syndrome; Waardenburg's syndrome; Waardenburg, types I and/or II
Alt IDs: MESH:D014849, NCI:C75008, NCI:C85222, OMIM:PS193500, ORDO:3440, ORDO:895, UMLS_CUI:C0079661, UMLS_CUI:C1847800, UMLS_CUI:C3266898
Definition: A syndrome characterized by varying degrees of deafness, minor defects in structures arising from the neural crest and pigmentation anomalies of the hair, the skin and/or the iris of both eyes.

Disease References using Mouse Models (22)
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory