abnormal speech discrimination Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A type of hearing impairment prominently characterized by a difficulty in understanding speech, rather than an inability to hear speech. Poor speech discrimination is a very common symptom of high frequency hearing loss. (Human Phenotype Ontology, HP_0001963)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001963
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Genes

1 genes associated with the abnormal speech discrimination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
DIAPH3 diaphanous-related formin 3