high-frequency sensorineural hearing impairment Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A form of sensorineural hearing impairment that affects primarily the higher frequencies. (Human Phenotype Ontology, HP_0001757)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001757
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Genes

2 genes associated with the high-frequency sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
FKBP14 FK506 binding protein 14, 22 kDa
MYH9 myosin, heavy chain 9, non-muscle