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Egenskap
EMG: neuropathic changes
The presence of characteristic findings of denervation on electromyography (fibrillations, positive sharp waves, and giant motor unit potentials).
Sammendrag
- Også kalt
- EMG: neurogenic abnormalities, EMG: neurogenic changes, EMG: neurogenic findings
- Kroppssystem
- Abnormality of the musculoskeletal system
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Denne siden som data
Legg til .json etter adressen til siden, eller be om application/json, for å lese den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/emg-neuropathic-changes.json"
page <- fromJSON(url)
page$trait$nameEMG: neuropathic changesHP:0003445
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Les genene knyttet til EMG: neuropathic changes, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test33 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.
- Spinal Muscular AtrophyReads 9 of these genesHSPB8UBA1CHCHD10ATP7ADYNC1H1IGHMBP2About this report →
- Charcot-Marie-Tooth DiseaseReads 14 of these genesHSPB8NEFHVCPGBF1HSPB1GJB1About this report →
- Distal MyopathiesReads 6 of these genesVCPANO5HNRNPA1HNRNPA2B1LDB3MYH7About this report →
- Rare Hereditary Peripheral NeuropathiesReads 19 of these genesHSPB8NEFHVCPGBF1HSPB1CHCHD10About this report →
Show 29 more reports
- Frontotemporal DementiaReads 4 of these genesVCPCHCHD10HNRNPA1HNRNPA2B1About this report →
- Hereditary Neuropathy with Liability to Pressure Palsies (HNPP)Reads 1 of these genesPMP22About this report →
- Inherited Neurodegenerative DisordersReads 19 of these genesHSPB8VCPUBA1CHCHD10SPG11VAPBAbout this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 5 of these genesVCPCHCHD10SPG11VAPBHNRNPA1About this report →
- Myofibrillar MyopathiesReads 3 of these genesHSPB8BAG3LDB3About this report →
- Left Ventricular NoncompactionReads 2 of these genesLDB3MYH7About this report →
- Metachromatic LeukodystrophyReads 1 of these genesARSAAbout this report →
- Congenital MyopathiesReads 3 of these genesACTA1MYH7NEBAbout this report →
- Disorder of Copper MetabolismReads 1 of these genesATP7AAbout this report →
- Neuroacanthocytosis and Huntington Disease PhenocopiesReads 1 of these genesVPS13AAbout this report →
- Dilated CardiomyopathyReads 4 of these genesBAG3SYNE1LDB3MYH7About this report →
- Familial Glucocorticoid DeficiencyReads 1 of these genesNDC1About this report →
- Neuronal Ceroid LipofuscinosisReads 1 of these genesTPP1About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 2 of these genesSYNE1TPP1About this report →
- Lysosomal Storage DiseaseReads 2 of these genesTPP1ARSAAbout this report →
- Complex Cortical Dysplasia and Frontoparietal PolymicrogyriaReads 1 of these genesDYNC1H1About this report →
- Hypertrophic CardiomyopathyReads 2 of these genesLDB3MYH7About this report →
- Cutis LaxaReads 1 of these genesATP7AAbout this report →
- Pontocerebellar Hypoplasia (TSEN54 and MINPP1)Reads 1 of these genesVRK1About this report →
- VitreoretinopathyReads 1 of these genesDYNC1H1About this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesANO5About this report →
- Osteogenesis ImperfectaReads 1 of these genesANO5About this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 1 of these genesNOP56About this report →
- Intellectual DisabilityReads 2 of these genesDYNC1H1VRK1About this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesSPG11About this report →
- Leigh SyndromeReads 1 of these genesPNPT1About this report →
- Other Inherited LeukodystrophiesReads 1 of these genesARSAAbout this report →
- Hearing Loss and DeafnessReads 1 of these genesPNPT1About this report →
- Primary Mitochondrial DiseaseReads 1 of these genesPNPT1About this report →
Les genene knyttet til EMG: neuropathic changes, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test36 gener knyttet til EMG: neuropathic changes
Endringer i disse genene forårsaker sjeldne tilstander der EMG: neuropathic changes forekommer. De fleste med denne egenskapen har ingen av disse tilstandene, og et gen på denne listen sier ingenting om noens eget genom.
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| HSPB3heat shock protein family B (small) member 3 | Alltid | I 1 tilstand |
| HSPB8heat shock protein family B (small) member 8 | Alltid | I 2 tilstander |
| NDC1NDC1 transmembrane nucleoporin | Alltid | I 1 tilstand |
| NEFHneurofilament heavy chain | Alltid | I 1 tilstand |
| VCPvalosin containing protein | Alltid | I 2 tilstander |
| WSB2WD repeat and SOCS box containing 2 | Alltid | I 1 tilstand |
| BAG3BAG cochaperone 3 | Svært ofte (80–99 %) | I 1 tilstand |
| GBF1golgi brefeldin A resistant guanine nucleotide exchange factor 1 | Svært ofte (80–99 %) | I 1 tilstand |
| HSPB1heat shock protein family B (small) member 1 | Svært ofte (80–99 %) | I 2 tilstander |
| UBA1ubiquitin like modifier activating enzyme 1 | Svært ofte (80–99 %) | I 1 tilstand |
| ANO5anoctamin 5 | Ofte (30–79 %) | I 1 tilstand |
| CHCHD10coiled-coil-helix-coiled-coil-helix domain containing 10 | Ofte (30–79 %) | I 1 tilstand |
| GJB1gap junction protein beta 1 | Ofte (30–79 %) | I 1 tilstand |
| IBA57iron-sulfur cluster assembly factor IBA57 | Ofte (30–79 %) | I 1 tilstand |
| PMP22peripheral myelin protein 22 | Ofte (30–79 %) | I 1 tilstand |
| PNPT1polyribonucleotide nucleotidyltransferase 1 | Ofte (30–79 %) | I 1 tilstand |
| SPG11SPG11 vesicle trafficking associated, spatacsin | Ofte (30–79 %) | I 1 tilstand |
| VAPBVAMP associated protein B and C | Ofte (30–79 %) | I 2 tilstander |
| VPS13Avacuolar protein sorting 13 homolog A | Ofte (30–79 %) | I 1 tilstand |
| HNRNPA1heterogeneous nuclear ribonucleoprotein A1 | Noen ganger (5–29 %) | I 1 tilstand |
| HNRNPA2B1heterogeneous nuclear ribonucleoprotein A2/B1 | Noen ganger (5–29 %) | I 1 tilstand |
| SYNE1spectrin repeat containing nuclear envelope protein 1 | Noen ganger (5–29 %) | I 1 tilstand |
| TPP1tripeptidyl peptidase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| ACTA1actin alpha 1, skeletal muscle | Ikke registrert | I 1 tilstand |
| ARSAarylsulfatase A | Ikke registrert | I 1 tilstand |
| ATP7AATPase copper transporting alpha | Ikke registrert | I 1 tilstand |
| DYNC1H1dynein cytoplasmic 1 heavy chain 1 | Ikke registrert | I 1 tilstand |
| GDAP1ganglioside induced differentiation associated protein 1 | Ikke registrert | I 1 tilstand |
| IGHMBP2immunoglobulin mu DNA binding protein 2 | Ikke registrert | I 1 tilstand |
| LDB3LIM domain binding 3 | Ikke registrert | I 1 tilstand |
| MYH7myosin heavy chain 7 | Ikke registrert | I 1 tilstand |
| NEBnebulin | Ikke registrert | I 1 tilstand |
| NOP56NOP56 ribonucleoprotein | Ikke registrert | I 1 tilstand |
| PLEKHG5pleckstrin homology and RhoGEF domain containing G5 | Ikke registrert | I 1 tilstand |
| SMN1survival of motor neuron 1, telomeric | Ikke registrert | I 2 tilstander |
| VRK1VRK serine/threonine kinase 1 | Ikke registrert | I 1 tilstand |
Hvor ofte dette forekommer hos personer med en av genets tilstander, oppgitt som den hyppigste forekomsten blant dem, slik Human Phenotype Ontology registrerer den. Disse sidene beskriver egenskaper og forskningen bak dem. De er ikke en diagnose, og om symptomer bør du spørre lege eller genetisk rådgiver.
Smalere egenskaper
Bredere egenskaper
Slik er informasjonen samlet
- Human Phenotype Ontology, versjon 2026-09-01: egenskapen, navnene på den, definisjonen og genene som er knyttet til den. Les mer på hpo.jax.org.
- Datautgave 2026.10.19-9814e911.
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Logg innSpørSekvenser genomet ditt↗
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Read the genes behind these traits in your own DNA.
The Genome Test sequences nearly all of your DNA, not a preset panel, so every gene on these pages is in your data. Premium adds 810+ physician-ready reports.
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