profound hearing impairment Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A profound (essentially complete) form of hearing impairment. (Human Phenotype Ontology, HP_0012715)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012715
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Genes

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

Symbol Name
CIB2 calcium and integrin binding family member 2
FGF3 fibroblast growth factor 3
MYO15A myosin XVA
RDX radixin
TBC1D24 TBC1 domain family, member 24