morphological abnormality of the vestibule of the inner ear Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A morphological abnormality of the vestibule, the central part of the osseous labyrinth that is situated medial to the tympanic cavity, behind the cochlea, and in front of the semicircular canals. (Human Phenotype Ontology, HP_0011376)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011376
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Genes

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

Symbol Name
FOXI1 forkhead box I1
KCNJ10 potassium channel, inwardly rectifying subfamily J, member 10
SLC26A4 solute carrier family 26 (anion exchanger), member 4
SOX10 SRY (sex determining region Y)-box 10