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Trait
EMG: myopathic abnormalities
The presence of abnormal electromyographic patterns indicative of myopathy, such as small-short polyphasic motor unit potentials.
Summary
- Also called
- EMG: myopathic changes, EMG: myopathy, Myopathic electromyogram
- Body system
- Abnormality of the musculoskeletal system
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This page as data
Add .json to the page's address, or ask for application/json, to read it as JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/emg-myopathic-abnormalities.json"
page <- fromJSON(url)
page$trait$nameEMG: myopathic abnormalitiesHP:0003458
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Get my Genome Test58 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.
- Distal MyopathiesReads 17 of these genesDNAJB4GIPC1MYH7ADSS1FLNCHNRNPA1About this report →
- Limb-Girdle Muscular DystrophyReads 18 of these genesCOL6A1SGCASNUPNTRIM32COL6A2COL6A3About this report →
- Myofibrillar MyopathiesReads 11 of these genesBAG3HSPB8FLNCCRYABMYOTRYR1About this report →
- Congenital MyopathiesReads 13 of these genesMYH7ACTA1KBTBD13KLHL41MYPNNEBAbout this report →
Show 54 more reports
- Congenital Muscular DystrophiesReads 11 of these genesCOL6A1SNUPNCOL12A1COL6A2COL6A3TRIP4About this report →
- Dilated CardiomyopathyReads 14 of these genesBAG3MYH7SGCAFHL1FLNCMYPNAbout this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 8 of these genesCDONDISP1GLI2PTCH1SHHSIX3About this report →
- Nevoid Basal Cell Carcinoma (Gorlin) SyndromeReads 2 of these genesPTCH1SUFUAbout this report →
- Tubular Aggregate MyopathyReads 2 of these genesORAI1STIM1About this report →
- Frontotemporal DementiaReads 5 of these genesSQSTM1HNRNPA1HNRNPA2B1VCPCHCHD10About this report →
- Danon DiseaseReads 1 of these genesLAMP2About this report →
- DLL1-Related Neurodevelopmental DisorderReads 1 of these genesDLL1About this report →
- Glycogen Storage Disease IXdReads 1 of these genesPHKA1About this report →
- MEGF10-Related MyopathyReads 1 of these genesMEGF10About this report →
- PLEC-Related Epidermolysis Bullosa and Muscular DystrophyReads 1 of these genesPLECAbout this report →
- Polyglucosan Body Myopathy 2 (GYG1)Reads 1 of these genesGYG1About this report →
- SCN4A-Related Congenital MyopathyReads 1 of these genesSCN4AAbout this report →
- UNC13A-Related Neurodevelopmental DisordersReads 1 of these genesUNC13AAbout this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 5 of these genesSQSTM1TUBA4AHNRNPA1VCPCHCHD10About this report →
- Charcot-Marie-Tooth DiseaseReads 8 of these genesHSPB8MPV17SCO2VCPDNM2LMNAAbout this report →
- Primary Mitochondrial DiseaseReads 9 of these genesMPV17SCO2SLC25A4ACAD9POLGPOLG2About this report →
- Left Ventricular NoncompactionReads 2 of these genesMYH7LDB3About this report →
- Rare Hereditary Peripheral NeuropathiesReads 11 of these genesHSPB8MPV17SCO2VCPDNM2LMNAAbout this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 2 of these genesLMNADESAbout this report →
- Fontaine Progeroid SyndromeReads 1 of these genesSLC25A4About this report →
- Malignant Hyperthermia SusceptibilityReads 1 of these genesRYR1About this report →
- Inherited Neurodegenerative DisordersReads 13 of these genesHSPB8SQSTM1TUBA4AHNRNPA1HNRNPA2B1TANGO2About this report →
- Hypertrophic CardiomyopathyReads 5 of these genesMYH7TRIM63FLNCMYPNLDB3About this report →
- Arrhythmogenic CardiomyopathyReads 2 of these genesTMEM43DESAbout this report →
- Familial Periodic ParalysisReads 1 of these genesSCN4AAbout this report →
- MedulloblastomaReads 1 of these genesSUFUAbout this report →
- Congenital Disorders of GlycosylationReads 5 of these genesCRPPAFKRPFKTNGNEPOMT1About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 3 of these genesCOL6A3CLCN1SCN4AAbout this report →
- Familial Paget Disease of BoneReads 1 of these genesSQSTM1About this report →
- Ehlers-Danlos SyndromeReads 2 of these genesCOL12A1PLOD1About this report →
- Hypogonadotropic HypogonadismReads 3 of these genesSMCHD1FGF8FGFR1About this report →
- Hereditary Congenital & Juvenile CataractReads 2 of these genesCRYABUNC45BAbout this report →
- Syndromic and Metabolic CardiomyopathiesReads 1 of these genesSLC25A4About this report →
- Lysosomal Storage DiseaseReads 3 of these genesABHD5GNELAMP2About this report →
- Congenital Myasthenic SyndromeReads 2 of these genesPLECSCN4AAbout this report →
- Spinal Muscular AtrophyReads 2 of these genesHSPB8CHCHD10About this report →
- Hereditary HypolipoproteinemiasReads 1 of these genesSAR1BAbout this report →
- Inherited ThrombocytopeniasReads 2 of these genesSTIM1GNEAbout this report →
- Heterotaxy & Laterality DefectsReads 1 of these genesNODALAbout this report →
- LipodystrophyReads 1 of these genesLMNAAbout this report →
- Female InfertilityReads 2 of these genesTUBA4ATWNKAbout this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 2 of these genesSYNE1TWNKAbout this report →
- Fatty Acid Oxidation & Carnitine Cycle DisordersReads 1 of these genesACAD9About this report →
- Epidermolysis BullosaReads 1 of these genesPLECAbout this report →
- Bardet-Biedl and Alström SyndromesReads 1 of these genesTRIM32About this report →
- Dyskeratosis CongenitaReads 1 of these genesDNMT3BAbout this report →
- Syndromic CraniosynostosisReads 1 of these genesFGFR1About this report →
- Microphthalmia, Anophthalmia & ColobomaReads 1 of these genesSHHAbout this report →
- Osteogenesis ImperfectaReads 1 of these genesANO5About this report →
- Joubert Syndrome And Related DisordersReads 1 of these genesSUFUAbout this report →
- Other Inborn Errors of ImmunityReads 2 of these genesORAI1STIM1About this report →
- Leigh SyndromeReads 1 of these genesSCO2About this report →
- Hearing Loss and DeafnessReads 1 of these genesMYH14About this report →
Read the genes linked to EMG: myopathic abnormalities, and the rest of your genome, with one test.
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Get my Genome Test119 genes linked to EMG: myopathic abnormalities
Changes in these genes cause rare conditions in which EMG: myopathic abnormalities 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 |
|---|---|---|
| BAG3BAG cochaperone 3 | Always | In 1 condition |
| COL6A1collagen type VI alpha 1 chain | Always | In 3 conditions |
| DNAJB4DnaJ heat shock protein family (Hsp40) member B4 | Always | In 1 condition |
| GIPC1GIPC PDZ domain containing family member 1 | Always | In 1 condition |
| HSPB8heat shock protein family B (small) member 8 | Always | In 1 condition |
| JPH1junctophilin 1 | Always | In 1 condition |
| MPV17mitochondrial inner membrane protein MPV17 | Always | In 1 condition |
| MYBPC1myosin binding protein C1 | Always | In 1 condition |
| MYH7myosin heavy chain 7 | Always | In 3 conditions |
| RILPL1Rab interacting lysosomal protein like 1 | Always | In 1 condition |
| SCO2synthesis of cytochrome C oxidase 2 | Always | In 1 condition |
| SGCAsarcoglycan alpha | Always | In 1 condition |
| SLC25A4solute carrier family 25 member 4 | Always | In 3 conditions |
| SNUPNsnurportin 1 | Always | In 1 condition |
| SQSTM1sequestosome 1 | Always | In 2 conditions |
| TRIM32tripartite motif containing 32 | Always | In 1 condition |
| TRIM63tripartite motif containing 63 | Always | In 1 condition |
| TUBA4Atubulin alpha 4a | Always | In 2 conditions |
| UNC13Aunc-13 homolog A | Always | In 1 condition |
| ACTA1actin alpha 1, skeletal muscle | Very often (80–99%) | In 4 conditions |
| ADSS1adenylosuccinate synthase 1 | Very often (80–99%) | In 1 condition |
| CASQ1calsequestrin 1 | Very often (80–99%) | In 1 condition |
| COL12A1collagen type XII alpha 1 chain | Very often (80–99%) | In 2 conditions |
| COL6A2collagen type VI alpha 2 chain | Very often (80–99%) | In 2 conditions |
| COL6A3collagen type VI alpha 3 chain | Very often (80–99%) | In 2 conditions |
| FHL1four and a half LIM domains 1 | Very often (80–99%) | In 2 conditions |
| FLNCfilamin C | Very often (80–99%) | In 1 condition |
| HNRNPA1heterogeneous nuclear ribonucleoprotein A1 | Very often (80–99%) | In 3 conditions |
| HNRNPA2B1heterogeneous nuclear ribonucleoprotein A2/B1 | Very often (80–99%) | In 1 condition |
| JAG2jagged canonical Notch ligand 2 | Very often (80–99%) | In 1 condition |
| KBTBD13kelch repeat and BTB domain containing 13 | Very often (80–99%) | In 1 condition |
| KLHL41kelch like family member 41 | Very often (80–99%) | In 2 conditions |
| KLHL9kelch like family member 9 | Very often (80–99%) | In 1 condition |
| LRP12LDL receptor related protein 12 | Very often (80–99%) | In 1 condition |
| MEGF10multiple EGF like domains 10 | Very often (80–99%) | In 1 condition |
| MYPNmyopalladin | Very often (80–99%) | In 1 condition |
| NEBnebulin | Very often (80–99%) | In 4 conditions |
| ORAI1ORAI calcium release-activated calcium modulator 1 | Very often (80–99%) | In 1 condition |
| STIM1stromal interaction molecule 1 | Very often (80–99%) | In 1 condition |
| TANGO2transport and golgi organization 2 homolog | Very often (80–99%) | In 1 condition |
Show 79 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| TIA1TIA1 cytotoxic granule associated RNA binding protein | Very often (80–99%) | In 1 condition |
| TPM2tropomyosin 2 | Very often (80–99%) | In 1 condition |
| TPM3tropomyosin 3 | Very often (80–99%) | In 3 conditions |
| TRIP4thyroid hormone receptor interactor 4 | Very often (80–99%) | In 1 condition |
| VCPvalosin containing protein | Very often (80–99%) | In 2 conditions |
| ABHD5abhydrolase domain containing 5, lysophosphatidic acid acyltransferase | Often (30–79%) | In 1 condition |
| ACAD9acyl-CoA dehydrogenase family member 9 | Often (30–79%) | In 1 condition |
| ALDOAaldolase, fructose-bisphosphate A | Often (30–79%) | In 1 condition |
| ANO5anoctamin 5 | Often (30–79%) | In 2 conditions |
| BIN1bridging integrator 1 | Often (30–79%) | In 2 conditions |
| CAV3caveolin 3 | Often (30–79%) | In 2 conditions |
| CRPPACDP-L-ribitol pyrophosphorylase A | Often (30–79%) | In 1 condition |
| CRYABcrystallin alpha B | Often (30–79%) | In 1 condition |
| DNM2dynamin 2 | Often (30–79%) | In 2 conditions |
| DNMT3BDNA methyltransferase 3 beta | Often (30–79%) | In 1 condition |
| DUX4double homeobox 4 | Often (30–79%) | In 1 condition |
| DUX4L1double homeobox 4 like 1 (pseudogene) | Often (30–79%) | In 1 condition |
| EMDemerin | Often (30–79%) | In 1 condition |
| FKRPfukutin related protein | Often (30–79%) | In 2 conditions |
| FKTNfukutin | Often (30–79%) | In 1 condition |
| FRG1FSHD region gene 1 | Often (30–79%) | In 1 condition |
| GNEglucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase | Often (30–79%) | In 2 conditions |
| GYG1glycogenin 1 | Often (30–79%) | In 1 condition |
| LMNAlamin A/C | Often (30–79%) | In 2 conditions |
| MSTO1misato mitochondrial distribution and morphology regulator 1 | Often (30–79%) | In 1 condition |
| MTMR14myotubularin related protein 14 | Often (30–79%) | In 2 conditions |
| MYF6myogenic factor 6 | Often (30–79%) | In 1 condition |
| MYH14myosin heavy chain 14 | Often (30–79%) | In 1 condition |
| MYOTmyotilin | Often (30–79%) | In 1 condition |
| NEFLneurofilament light chain | Often (30–79%) | In 1 condition |
| PHKA1phosphorylase kinase regulatory subunit alpha 1 | Often (30–79%) | In 1 condition |
| PHKG1phosphorylase kinase catalytic subunit gamma 1 | Often (30–79%) | In 1 condition |
| PLECplectin | Often (30–79%) | In 1 condition |
| POLGDNA polymerase gamma, catalytic subunit | Often (30–79%) | In 3 conditions |
| POLG2DNA polymerase gamma 2, accessory subunit | Often (30–79%) | In 1 condition |
| POMT1protein O-mannosyltransferase 1 | Often (30–79%) | In 1 condition |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Often (30–79%) | In 1 condition |
| RYR1ryanodine receptor 1 | Often (30–79%) | In 2 conditions |
| SGCGsarcoglycan gamma | Often (30–79%) | In 1 condition |
| SMCHD1structural maintenance of chromosomes flexible hinge domain containing 1 | Often (30–79%) | In 1 condition |
| SVILsupervillin | Often (30–79%) | In 1 condition |
| SYNE1spectrin repeat containing nuclear envelope protein 1 | Often (30–79%) | In 1 condition |
| SYNE2spectrin repeat containing nuclear envelope protein 2 | Often (30–79%) | In 1 condition |
| TMEM43transmembrane protein 43 | Often (30–79%) | In 1 condition |
| TNNT1troponin T1, slow skeletal type | Often (30–79%) | In 1 condition |
| TTNtitin | Often (30–79%) | In 4 conditions |
| TWNKtwinkle mtDNA helicase | Often (30–79%) | In 2 conditions |
| UNC45Bunc-45 myosin chaperone B | Often (30–79%) | In 1 condition |
| CDONcell adhesion associated, oncogene regulated | Sometimes (5–29%) | In 1 condition |
| CHCHD10coiled-coil-helix-coiled-coil-helix domain containing 10 | Sometimes (5–29%) | In 1 condition |
| CLCN1chloride voltage-gated channel 1 | Sometimes (5–29%) | In 1 condition |
| CRIPTOcripto, EGF-CFC family member | Sometimes (5–29%) | In 1 condition |
| DHX16DEAH-box helicase 16 | Sometimes (5–29%) | In 1 condition |
| DISP1dispatched RND transporter family member 1 | Sometimes (5–29%) | In 1 condition |
| DLL1delta like canonical Notch ligand 1 | Sometimes (5–29%) | In 1 condition |
| FGF8fibroblast growth factor 8 | Sometimes (5–29%) | In 1 condition |
| FGFR1fibroblast growth factor receptor 1 | Sometimes (5–29%) | In 1 condition |
| FOXH1forkhead box H1 | Sometimes (5–29%) | In 1 condition |
| GAS1growth arrest specific 1 | Sometimes (5–29%) | In 1 condition |
| GLI2GLI family zinc finger 2 | Sometimes (5–29%) | In 1 condition |
| NODALnodal growth differentiation factor | Sometimes (5–29%) | In 1 condition |
| PLOD1procollagen-lysine,2-oxoglutarate 5-dioxygenase 1 | Sometimes (5–29%) | In 1 condition |
| PTCH1patched 1 | Sometimes (5–29%) | In 1 condition |
| SAR1Bsecretion associated Ras related GTPase 1B | Sometimes (5–29%) | In 1 condition |
| SCN4Asodium voltage-gated channel alpha subunit 4 | Sometimes (5–29%) | In 1 condition |
| SHHsonic hedgehog signaling molecule | Sometimes (5–29%) | In 1 condition |
| SIX3SIX homeobox 3 | Sometimes (5–29%) | In 1 condition |
| SUFUSUFU negative regulator of hedgehog signaling | Sometimes (5–29%) | In 1 condition |
| TGIF1TGFB induced factor homeobox 1 | Sometimes (5–29%) | In 1 condition |
| VWA1von Willebrand factor A domain containing 1 | Sometimes (5–29%) | In 1 condition |
| ZIC2Zic family zinc finger 2 | Sometimes (5–29%) | In 1 condition |
| DESdesmin | Not recorded | In 1 condition |
| DYSFdysferlin | Not recorded | In 1 condition |
| FXR1FMR1 autosomal homolog 1 | Not recorded | In 1 condition |
| LAMP2lysosome associated membrane protein 2 | Not recorded | In 1 condition |
| LARGE1LARGE xylosyl- and glucuronyltransferase 1 | Not recorded | In 1 condition |
| LDB3LIM domain binding 3 | Not recorded | In 1 condition |
| TK2thymidine kinase 2 | Not recorded | In 1 condition |
| TNPO3transportin 3 | 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.
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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