aplasia/hypoplasia of the cochlea Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence or underdevelopment of the cochlea, a spiral shaped cavity in the inner ear, owing to a developmental defect. (Human Phenotype Ontology, HP_0011395)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011395
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Genes

2 genes associated with the aplasia/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