Trait
Progressive hearing impairment
A form of hearing impairment that remains stable over time.
Summary
- Also called
- Progressive hearing loss
- Body system
- Abnormality of the ear
Reference genomeGRCh38hg38
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Get my Genome Test10 genes linked to Progressive hearing impairment
Changes in these genes cause rare conditions in which Progressive hearing impairment is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.
| Gene | How often it is seen | Conditions |
|---|---|---|
| PEX11Bperoxisomal biogenesis factor 11 beta | Always | In 1 condition |
| TBC1D24TBC1 domain family member 24 | Always | In 1 condition |
| DMXL2Dmx like 2 | Often (30–79%) | In 2 conditions |
| GOSR2golgi SNAP receptor complex member 2 | Often (30–79%) | In 1 condition |
| POLR3GLRNA polymerase III subunit GL | Often (30–79%) | In 1 condition |
| WFS1wolframin ER transmembrane glycoprotein | Often (30–79%) | In 1 condition |
| TWNKtwinkle mtDNA helicase | Sometimes (5–29%) | In 1 condition |
| MIR96microRNA 96 | Not recorded | In 1 condition |
| MYO3Amyosin IIIA | Not recorded | In 1 condition |
| SERPINB6serpin family B member 6 | Not recorded | In 1 condition |
How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.
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Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
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