| 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 |
| Similar Terms | |
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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 |