hypoplasia of the cochlea Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Developmental hypoplasia of the cochlea. (Human Phenotype Ontology, HP_0008586)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008586
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2 genes associated with the hypoplasia of the cochlea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
DDX11 DEAD/H (Asp-Glu-Ala-Asp/His) box helicase 11
EYA1 EYA transcriptional coactivator and phosphatase 1