morphological abnormality of the inner ear Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	A structural anomaly of the internal part of the ear. (Human Phenotype Ontology, HP_0011390)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0011390
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Genes

11 genes associated with the morphological abnormality of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol	Name
COCH	cochlin
COL4A6	collagen, type IV, alpha 6
DDX11	DEAD/H (Asp-Glu-Ala-Asp/His) box helicase 11
EYA1	EYA transcriptional coactivator and phosphatase 1
FGF3	fibroblast growth factor 3
FOXI1	forkhead box I1
KCNJ10	potassium channel, inwardly rectifying subfamily J, member 10
ORC1	origin recognition complex, subunit 1
POU3F4	POU class 3 homeobox 4
SLC26A4	solute carrier family 26 (anion exchanger), member 4
SOX10	SRY (sex determining region Y)-box 10