Trait
Abnormal auditory evoked potentials
An abnormality of the auditory evoked potentials, which are used to trace the signal generated by a sound, from the cochlear nerve, through the lateral lemniscus, to the medial geniculate nucleus, and to the cortex.
Summary
- Also called
- Abnormal brainstem auditory-evoked potentials
- Body system
- Abnormality of the nervous system
Read the genes linked to Abnormal auditory evoked potentials, and the rest of your genome, with one test.
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Get my Genome Test14 genes linked to Abnormal auditory evoked potentials
Changes in these genes cause rare conditions in which Abnormal auditory evoked potentials 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 |
|---|---|---|
| EDNRBendothelin receptor type B | Always | In 1 condition |
| NMNAT1nicotinamide nucleotide adenylyltransferase 1 | Always | In 1 condition |
| GJC2gap junction protein gamma 2 | Very often (80–99%) | In 1 condition |
| ARHGEF2Rho/Rac guanine nucleotide exchange factor 2 | Often (30–79%) | In 1 condition |
| CYP27A1cytochrome P450 family 27 subfamily A member 1 | Often (30–79%) | In 1 condition |
| EBPEBP cholestenol delta-isomerase | Often (30–79%) | In 1 condition |
| LMNB1lamin B1 | Often (30–79%) | In 1 condition |
| DIAPH3diaphanous related formin 3 | Not recorded | In 1 condition |
| ERCC6ERCC excision repair 6, chromatin remodeling factor | Not recorded | In 1 condition |
| ERCC8ERCC excision repair 8, CSA ubiquitin ligase complex subunit | Not recorded | In 1 condition |
| MTMR2myotubularin related protein 2 | Not recorded | In 1 condition |
| MYH3myosin heavy chain 3 | Not recorded | In 1 condition |
| NDRG1N-myc downstream regulated 1 | Not recorded | In 1 condition |
| OPA1OPA1 mitochondrial dynamin like GTPase | 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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