AtlasKenmerk
Exercise-induced muscle pain
Klinische naam: Exercise-induced myalgia
The occurrence of an unusually high amount of muscle pain following exercise.
Samenvatting
- Ook bekend als
- Muscle pain on exercise, Muscle pain with exercise, Muscle pain, exercise-induced
- Lichaamssysteem
- Constitutional symptom
AtlasDeze pagina als gegevens
Voeg .json toe aan het adres van de pagina, of vraag application/json aan, om haar als JSON te lezen.
library(jsonlite)
url <- "https://dantelabs.com/traits/exercise-induced-myalgia.json"
page <- fromJSON(url)
page$trait$nameLees de genen die aan Exercise-induced muscle pain gekoppeld zijn, en de rest van uw genoom, met één test.
Vanaf $ 449Gratis verzending · Resultaten binnen 6–8 weken
Mijn Genome Test bestellen27 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 5 of these genesFLNCANO5DYSFHNRNPA1MATR3About this report →
- Glycogen Storage DiseaseReads 4 of these genesGYS1LDHAPGK1PGAM2About this report →
- Limb-Girdle Muscular DystrophyReads 6 of these genesHMGCRLMNAANO5DYSFCAV3TRIM32About this report →
- Glycogen Storage Disease IXdReads 1 of these genesPHKA1About this report →
Show 23 more reports
- Hereditary Neuropathy with Liability to Pressure Palsies (HNPP)Reads 1 of these genesPMP22About this report →
- LPIN1-Related Recurrent RhabdomyolysisReads 1 of these genesLPIN1About this report →
- McArdle's diseaseReads 1 of these genesPYGMAbout this report →
- Very Long Chain Acyl-Coa Dehydrogenase DeficiencyReads 1 of these genesACADVLAbout this report →
- Congenital MyopathiesReads 4 of these genesBIN1DNM2RYR1TPM2About this report →
- Fatty Acid Oxidation & Carnitine Cycle DisordersReads 3 of these genesCPT2ACADMACADVLAbout this report →
- Malignant Hyperthermia SusceptibilityReads 1 of these genesRYR1About this report →
- Tubular Aggregate MyopathyReads 1 of these genesSTIM1About this report →
- Myofibrillar MyopathiesReads 2 of these genesFLNCRYR1About this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 2 of these genesHNRNPA1MATR3About this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesLMNAAbout this report →
- Charcot-Marie-Tooth DiseaseReads 3 of these genesLMNADNM2PMP22About this report →
- LipodystrophyReads 1 of these genesLMNAAbout this report →
- Dilated CardiomyopathyReads 2 of these genesLMNAFLNCAbout this report →
- Frontotemporal DementiaReads 1 of these genesHNRNPA1About this report →
- Rare Hereditary Peripheral NeuropathiesReads 4 of these genesLMNARRM2BDNM2PMP22About this report →
- Primary Mitochondrial DiseaseReads 3 of these genesTMEM126BRNASEH1RRM2BAbout this report →
- Hypertrophic CardiomyopathyReads 2 of these genesFLNCACADVLAbout this report →
- Bardet-Biedl and Alström SyndromesReads 1 of these genesTRIM32About this report →
- Inherited ThrombocytopeniasReads 1 of these genesSTIM1About this report →
- Osteogenesis ImperfectaReads 1 of these genesANO5About this report →
- Inherited Neurodegenerative DisordersReads 2 of these genesHNRNPA1MATR3About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesSTIM1About this report →
Lees de genen die aan Exercise-induced muscle pain gekoppeld zijn, en de rest van uw genoom, met één test.
Vanaf $ 449Gratis verzending · Resultaten binnen 6–8 weken
Mijn Genome Test bestellen39 genen gekoppeld aan Exercise-induced muscle pain
Veranderingen in deze genen veroorzaken zeldzame aandoeningen waarbij Exercise-induced muscle pain voorkomt. De meeste mensen met dit kenmerk hebben geen van die aandoeningen, en een gen op deze lijst zegt niets over het eigen genoom van iemand.
| Gen | Hoe vaak het voorkomt | Aandoeningen |
|---|---|---|
| FILIP1filamin A interacting protein 1 | Altijd | In 1 aandoening |
| GYS1glycogen synthase 1 | Altijd | In 1 aandoening |
| HMGCR3-hydroxy-3-methylglutaryl-CoA reductase | Altijd | In 1 aandoening |
| LMNAlamin A/C | Altijd | In 2 aandoeningen |
| SLC25A42solute carrier family 25 member 42 | Altijd | In 1 aandoening |
| TMEM126Btransmembrane protein 126B | Altijd | In 1 aandoening |
| AMPD1adenosine monophosphate deaminase 1 | Heel vaak (80–99%) | In 2 aandoeningen |
| AMPD3adenosine monophosphate deaminase 3 | Heel vaak (80–99%) | In 1 aandoening |
| CPT2carnitine palmitoyltransferase 2 | Heel vaak (80–99%) | In 2 aandoeningen |
| FLNCfilamin C | Heel vaak (80–99%) | In 1 aandoening |
| ACADMacyl-CoA dehydrogenase medium chain | Vaak (30–79%) | In 1 aandoening |
| ANO5anoctamin 5 | Vaak (30–79%) | In 1 aandoening |
| DYSFdysferlin | Vaak (30–79%) | In 2 aandoeningen |
| HNRNPA1heterogeneous nuclear ribonucleoprotein A1 | Vaak (30–79%) | In 1 aandoening |
| LDHAlactate dehydrogenase A | Vaak (30–79%) | In 1 aandoening |
| LPIN1lipin 1 | Vaak (30–79%) | In 1 aandoening |
| MATR3matrin 3 | Vaak (30–79%) | In 1 aandoening |
| MLIPmuscular LMNA interacting protein | Vaak (30–79%) | In 1 aandoening |
| MT-CO1mitochondrially encoded cytochrome c oxidase I | Vaak (30–79%) | In 1 aandoening |
| MT-CO3mitochondrially encoded cytochrome c oxidase III | Vaak (30–79%) | In 1 aandoening |
| OBSCNobscurin, cytoskeletal calmodulin and titin-interacting RhoGEF | Vaak (30–79%) | In 1 aandoening |
| PFKMphosphofructokinase, muscle | Vaak (30–79%) | In 1 aandoening |
| PGK1phosphoglycerate kinase 1 | Vaak (30–79%) | In 1 aandoening |
| RNASEH1ribonuclease H1 | Vaak (30–79%) | In 1 aandoening |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Vaak (30–79%) | In 1 aandoening |
| BIN1bridging integrator 1 | Soms (5–29%) | In 1 aandoening |
| DNM2dynamin 2 | Soms (5–29%) | In 1 aandoening |
| MTMR14myotubularin related protein 14 | Soms (5–29%) | In 1 aandoening |
| MYF6myogenic factor 6 | Soms (5–29%) | In 1 aandoening |
| PMP22peripheral myelin protein 22 | Soms (5–29%) | In 1 aandoening |
| PYGMglycogen phosphorylase, muscle associated | Soms (5–29%) | In 2 aandoeningen |
| RYR1ryanodine receptor 1 | Soms (5–29%) | In 3 aandoeningen |
| TPM2tropomyosin 2 | Soms (5–29%) | In 1 aandoening |
| ACADVLacyl-CoA dehydrogenase very long chain | Niet vastgelegd | In 1 aandoening |
| CAV3caveolin 3 | Niet vastgelegd | In 1 aandoening |
| PGAM2phosphoglycerate mutase 2 | Niet vastgelegd | In 1 aandoening |
| PHKA1phosphorylase kinase regulatory subunit alpha 1 | Niet vastgelegd | In 1 aandoening |
| STIM1stromal interaction molecule 1 | Niet vastgelegd | In 1 aandoening |
| TRIM32tripartite motif containing 32 | Niet vastgelegd | In 1 aandoening |
Hoe vaak dit voorkomt bij mensen met een van de aandoeningen van het gen, de hoogste frequentie binnen die aandoeningen, zoals de Human Phenotype Ontology dit vastlegt. Deze pagina's beschrijven kenmerken en het onderzoek erachter; het zijn geen diagnose, en over symptomen kunt u het best een arts of genetisch adviseur raadplegen.
Bredere kenmerken
Waar dit vandaan komt
- De Human Phenotype Ontology, release 2026-09-01: het kenmerk, de namen, de definitie en de genen die ermee verbonden zijn. Meer informatie vindt u op hpo.jax.org.
- Gegevensrelease 2026.10.19-9814e911.
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