Trait
EMG: neuropathic changes
The presence of characteristic findings of denervation on electromyography (fibrillations, positive sharp waves, and giant motor unit potentials).
Summary
- Also called
- EMG: neurogenic abnormalities, EMG: neurogenic changes, EMG: neurogenic findings
- Body system
- Abnormality of the musculoskeletal system
Reference genomeGRCh38hg38
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Read the genes linked to EMG: neuropathic changes, and the rest of your genome, with one test.
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Get my Genome Test36 genes linked to EMG: neuropathic changes
Changes in these genes cause rare conditions in which EMG: neuropathic changes 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 |
|---|---|---|
| HSPB3heat shock protein family B (small) member 3 | Always | In 1 condition |
| HSPB8heat shock protein family B (small) member 8 | Always | In 2 conditions |
| NDC1NDC1 transmembrane nucleoporin | Always | In 1 condition |
| NEFHneurofilament heavy chain | Always | In 1 condition |
| VCPvalosin containing protein | Always | In 2 conditions |
| WSB2WD repeat and SOCS box containing 2 | Always | In 1 condition |
| BAG3BAG cochaperone 3 | Very often (80–99%) | In 1 condition |
| GBF1golgi brefeldin A resistant guanine nucleotide exchange factor 1 | Very often (80–99%) | In 1 condition |
| HSPB1heat shock protein family B (small) member 1 | Very often (80–99%) | In 2 conditions |
| UBA1ubiquitin like modifier activating enzyme 1 | Very often (80–99%) | In 1 condition |
| ANO5anoctamin 5 | Often (30–79%) | In 1 condition |
| CHCHD10coiled-coil-helix-coiled-coil-helix domain containing 10 | Often (30–79%) | In 1 condition |
| GJB1gap junction protein beta 1 | Often (30–79%) | In 1 condition |
| IBA57iron-sulfur cluster assembly factor IBA57 | Often (30–79%) | In 1 condition |
| PMP22peripheral myelin protein 22 | Often (30–79%) | In 1 condition |
| PNPT1polyribonucleotide nucleotidyltransferase 1 | Often (30–79%) | In 1 condition |
| SPG11SPG11 vesicle trafficking associated, spatacsin | Often (30–79%) | In 1 condition |
| VAPBVAMP associated protein B and C | Often (30–79%) | In 2 conditions |
| VPS13Avacuolar protein sorting 13 homolog A | Often (30–79%) | In 1 condition |
| HNRNPA1heterogeneous nuclear ribonucleoprotein A1 | Sometimes (5–29%) | In 1 condition |
| HNRNPA2B1heterogeneous nuclear ribonucleoprotein A2/B1 | Sometimes (5–29%) | In 1 condition |
| SYNE1spectrin repeat containing nuclear envelope protein 1 | Sometimes (5–29%) | In 1 condition |
| TPP1tripeptidyl peptidase 1 | Sometimes (5–29%) | In 1 condition |
| ACTA1actin alpha 1, skeletal muscle | Not recorded | In 1 condition |
| ARSAarylsulfatase A | Not recorded | In 1 condition |
| ATP7AATPase copper transporting alpha | Not recorded | In 1 condition |
| DYNC1H1dynein cytoplasmic 1 heavy chain 1 | Not recorded | In 1 condition |
| GDAP1ganglioside induced differentiation associated protein 1 | Not recorded | In 1 condition |
| IGHMBP2immunoglobulin mu DNA binding protein 2 | Not recorded | In 1 condition |
| LDB3LIM domain binding 3 | Not recorded | In 1 condition |
| MYH7myosin heavy chain 7 | Not recorded | In 1 condition |
| NEBnebulin | Not recorded | In 1 condition |
| NOP56NOP56 ribonucleoprotein | Not recorded | In 1 condition |
| PLEKHG5pleckstrin homology and RhoGEF domain containing G5 | Not recorded | In 1 condition |
| SMN1survival of motor neuron 1, telomeric | Not recorded | In 2 conditions |
| VRK1VRK serine/threonine kinase 1 | 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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