bilateral conductive hearing impairment Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A bilateral type of conductive hearing impairment. (Human Phenotype Ontology, HP_0008513)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008513
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Genes

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

Symbol Name
EDN1 endothelin 1
SQSTM1 sequestosome 1
TNFRSF11A tumor necrosis factor receptor superfamily, member 11a, NFKB activator