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Disease Ontology Browser
Waardenburg's syndrome (DOID:9258)
Alliance: disease page
Synonyms: van der Hoeve Halbertsona Waardenburg syndrome; Waardenburg Shah syndrome; Waardenburg 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)
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last database update
09/27/2022
MGI 6.21
The Jackson Laboratory