vestibular hypofunction Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Reduced functioning of the vestibular apparatus. (Human Phenotype Ontology, HP_0001756)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001756
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Genes

5 genes associated with the vestibular hypofunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
MITF microphthalmia-associated transcription factor
MYO7A myosin VIIA
OTOGL otogelin-like
TYR tyrosinase
USH1C Usher syndrome 1C (autosomal recessive, severe)