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Disease Ontology Browser
Waardenburg's syndrome (DOID:9258)
Synonyms: van der Hoeve Halbertsona Waardenburg syndrome; Waardenburg Shah syndrome; Waardenburg syndrome; Waardenburg, types I and/or II; Waardenburg-Klein syndrome
Alt IDs: OMIM:148820, OMIM:193500, OMIM:193510, OMIM:277580, OMIM:600193, OMIM:606662, OMIM:608890, OMIM:611584, OMIM:613265, OMIM:613266, MESH:D014849, NCI:C75008, NCI:C85222, ORDO:3440, ORDO:894, ORDO:895, ORDO:896, UMLS_CUI:C0079661, UMLS_CUI:C1847800, UMLS_CUI:C3266898
Definition: An autosomal disease 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 (18)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
03/14/2017
MGI 6.08
The Jackson Laboratory