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page$trait$nameRead the genes linked to Limb myoclonus, and the rest of your genome, with one test.
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Get my Genome Test22 condition reports read genes linked to this trait
Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.
- Genetic Prion Disease (incl. Fatal Familial Insomnia)Reads 1 of these genesPRNPAbout this report →
- KCNQ2-Related Neonatal Encephalopathy with Non-Epileptic MyoclonusReads 1 of these genesKCNQ2About this report →
- Rett Syndrome and MECP2-Related DisordersReads 1 of these genesMECP2About this report →
- X-Linked Adrenoleukodystrophy (ABCD1)Reads 1 of these genesABCD1About this report →
Show 18 more reports
- Epilepsy (Full Panel)Reads 13 of these genesSCN8ACDKL5GABBR2KCNQ2KCNQ3MECP2About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 4 of these genesSGCEKCTD17TOR1APRRT2About this report →
- Hereditary Episodic AtaxiasReads 1 of these genesSCN2AAbout this report →
- Cornelia de Lange SyndromeReads 1 of these genesSMC1AAbout this report →
- Inherited Neurodegenerative DisordersReads 7 of these genesMAPTABCD1ASAH1KCTD7PRDX3PRNPAbout this report →
- Frontotemporal DementiaReads 1 of these genesMAPTAbout this report →
- Neuronal Ceroid LipofuscinosisReads 1 of these genesKCTD7About this report →
- Lysosomal Storage DiseaseReads 2 of these genesASAH1KCTD7About this report →
- Monogenic Hypertension & Mineralocorticoid DisordersReads 1 of these genesCACNA1HAbout this report →
- Parkinson DiseaseReads 1 of these genesMAPTAbout this report →
- Hereditary Corneal DystrophiesReads 1 of these genesPRDX3About this report →
- Spinal Muscular AtrophyReads 1 of these genesASAH1About this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 1 of these genesNOP56About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesPRDX3About this report →
- Intellectual DisabilityReads 2 of these genesMECP2SCN2AAbout this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesABCD1About this report →
- Other Inherited LeukodystrophiesReads 1 of these genesABCD1About this report →
- Congenital Disorders of GlycosylationReads 1 of these genesKCTD7About this report →
Read the genes linked to Limb myoclonus, and the rest of your genome, with one test.
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Get my Genome Test26 genes linked to Limb myoclonus
Changes in these genes cause rare conditions in which Limb myoclonus 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 |
|---|---|---|
| SCN8Asodium voltage-gated channel alpha subunit 8 | Always | In 2 conditions |
| SGCEsarcoglycan epsilon | Always | In 2 conditions |
| DRD2dopamine receptor D2 | Very often (80–99%) | In 1 condition |
| KCTD17potassium channel tetramerization domain containing 17 | Very often (80–99%) | In 1 condition |
| TOR1Atorsin family 1 member A | Very often (80–99%) | In 1 condition |
| CDKL5cyclin dependent kinase like 5 | Often (30–79%) | In 1 condition |
| GABBR2gamma-aminobutyric acid type B receptor subunit 2 | Often (30–79%) | In 1 condition |
| KCNQ2potassium voltage-gated channel subfamily Q member 2 | Often (30–79%) | In 2 conditions |
| KCNQ3potassium voltage-gated channel subfamily Q member 3 | Often (30–79%) | In 2 conditions |
| MAPTmicrotubule associated protein tau | Often (30–79%) | In 1 condition |
| MECP2methyl-CpG binding protein 2 | Often (30–79%) | In 1 condition |
| NTNG1netrin G1 | Often (30–79%) | In 1 condition |
| SMC1Astructural maintenance of chromosomes 1A | Often (30–79%) | In 1 condition |
| ABCD1ATP binding cassette subfamily D member 1 | Sometimes (5–29%) | In 1 condition |
| ASAH1N-acylsphingosine amidohydrolase 1 | Sometimes (5–29%) | In 1 condition |
| KCTD7potassium channel tetramerization domain containing 7 | Sometimes (5–29%) | In 1 condition |
| PRDX3peroxiredoxin 3 | Sometimes (5–29%) | In 1 condition |
| PRNPprion protein (Kanno blood group) | Sometimes (5–29%) | In 1 condition |
| PRRT2proline rich transmembrane protein 2 | Sometimes (5–29%) | In 1 condition |
| SCN2Asodium voltage-gated channel alpha subunit 2 | Sometimes (5–29%) | In 1 condition |
| CACNA1Hcalcium voltage-gated channel subunit alpha1 H | Rarely (1–4%) | In 1 condition |
| GABRA1gamma-aminobutyric acid type A receptor subunit alpha1 | Rarely (1–4%) | In 1 condition |
| GABRB3gamma-aminobutyric acid type A receptor subunit beta3 | Rarely (1–4%) | In 1 condition |
| GABRG2gamma-aminobutyric acid type A receptor subunit gamma2 | Rarely (1–4%) | In 1 condition |
| JRKJrk helix-turn-helix protein | Rarely (1–4%) | In 1 condition |
| NOP56NOP56 ribonucleoprotein | Rarely (1–4%) | 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.
Broader traits
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 2026.10.19-9814e911.
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