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)
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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