bilateral sensorineural hearing impairment Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A bilateral form of sensorineural hearing impairment. (Human Phenotype Ontology, HP_0008619)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008619
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Genes

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

Symbol Name
ACOX1 acyl-CoA oxidase 1, palmitoyl
ACTG1 actin gamma 1
ATP6V0A4 ATPase, H+ transporting, lysosomal V0 subunit a4
CHSY1 chondroitin sulfate synthase 1
DSPP dentin sialophosphoprotein
MITF microphthalmia-associated transcription factor
MYH9 myosin, heavy chain 9, non-muscle
MYO7A myosin VIIA
TBC1D24 TBC1 domain family, member 24