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DOID:9258 - Waardenburg syndrome
Disease Ontology 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.
Synonyms: van der Hoeve Halbertsona Waardenburg syndrome, Waardenburg Shah syndrome, Waardenburg's syndrome, Waardenburg syndrome, Waardenburg, types I and/or II
Xenbase Genes
:
sox10,
pax3,
mitf,
ednrb,
edn3
| MONDO:0018094 - Waardenburg syndrome |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
autosomal dominant disease (is_a),
syndrome (is_a)