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Cecha
Generalized muscle weakness
Generalized weakness or decreased strength of the muscles, affecting both distal and proximal musculature.
Podsumowanie
- Znana także jako
- Generalised muscle weakness, Generalised weakness, Generalized weakness, Muscle weakness, diffuse, Muscle weakness, generalised, Muscle weakness, generalized
- Układ organizmu
- Abnormality of the musculoskeletal system
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library(jsonlite)
url <- "https://dantelabs.com/traits/generalized-muscle-weakness.json"
page <- fromJSON(url)
page$trait$nameGeneralized muscle weaknessHP:0003324
AtlasDla kogo jest Dante LabsNasza naukaProduktyWyniki
Zaloguj sięZapytajZsekwencjonuj swój genom↗
Odczytaj geny powiązane z Generalized muscle weakness oraz resztę swojego genomu za pomocą jednego badania.
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Zamawiam Genome Test76 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.
- Amyotrophic Lateral Sclerosis (ALS)Reads 21 of these genesSPTLC1VCPANGANXA11CCNFCHCHD10About this report →
- Congenital MyopathiesReads 12 of these genesACTA1LMOD3RYR1TTNKLHL41NEBAbout this report →
- Congenital Muscular DystrophiesReads 12 of these genesFKRPFKTNPOMT2COL12A1COL6A1COL6A2About this report →
- Frontotemporal DementiaReads 7 of these genesVCPCCNFCHCHD10CHMP2BHNRNPA1SQSTM1About this report →
Show 72 more reports
- Limb-Girdle Muscular DystrophyReads 10 of these genesFKRPFKTNTTNCAPN3COL6A1COL6A2About this report →
- Inherited Neurodegenerative DisordersReads 32 of these genesSPTLC1VCPANGANXA11ATXN2CCNFAbout this report →
- Distal MyopathiesReads 7 of these genesTTNVCPHNRNPA1LRP12MATR3LDB3About this report →
- Congenital Myasthenic SyndromeReads 8 of these genesCHRNDMUSKSCN4ACOL13A1COLQCHRNA1About this report →
- Bartter DiseaseReads 3 of these genesCLCNKBKCNJ1SLC12A1About this report →
- Myofibrillar MyopathiesReads 4 of these genesRYR1TTNBAG3LDB3About this report →
- Malignant Endocrine NeoplasmReads 3 of these genesMEN1SDHASDHBAbout this report →
- ADCY5-Related DyskinesiaReads 1 of these genesADCY5About this report →
- Aminoacylase 1 DeficiencyReads 1 of these genesACY1About this report →
- Amyotrophic Lateral Sclerosis Susceptibility 24 (NEK1)Reads 1 of these genesNEK1About this report →
- Dystrophinopathies (Duchenne and Becker Muscular Dystrophy)Reads 1 of these genesDMDAbout this report →
- Gitelman SyndromeReads 1 of these genesSLC12A3About this report →
- Huntington DiseaseReads 1 of these genesHTTAbout this report →
- MEGF10-Related MyopathyReads 1 of these genesMEGF10About this report →
- MYH2-Related MyopathyReads 1 of these genesMYH2About this report →
- OPTN-Related Normal-Tension GlaucomaReads 1 of these genesOPTNAbout this report →
- PLEC-Related Epidermolysis Bullosa and Muscular DystrophyReads 1 of these genesPLECAbout this report →
- Pompe DiseaseReads 1 of these genesGAAAbout this report →
- SCN4A-Related Congenital MyopathyReads 1 of these genesSCN4AAbout this report →
- UNC13A-Related Neurodevelopmental DisordersReads 1 of these genesUNC13AAbout this report →
- Hereditary Pheochromocytoma and ParagangliomaReads 3 of these genesSDHASDHBSDHDAbout this report →
- Dilated CardiomyopathyReads 6 of these genesFKTNTTNBAG3DMDLDB3MYH7About this report →
- Syndromic and Metabolic CardiomyopathiesReads 2 of these genesAGKSLC25A4About this report →
- Congenital Disorders of GlycosylationReads 8 of these genesDSEFKRPFKTNPOMT2CRPPAPOMT1About this report →
- Rare Hereditary Peripheral NeuropathiesReads 12 of these genesSPTLC1VCPAIFM1CHCHD10DCTN1FIG4About this report →
- Left Ventricular NoncompactionReads 2 of these genesLDB3MYH7About this report →
- Fatty Acid Oxidation & Carnitine Cycle DisordersReads 3 of these genesACAD9HADHAHADHBAbout this report →
- Fontaine Progeroid SyndromeReads 1 of these genesSLC25A4About this report →
- Malignant Hyperthermia SusceptibilityReads 1 of these genesRYR1About this report →
- Riboflavin Transporter DeficiencyReads 1 of these genesSLC52A3About this report →
- Tubular Aggregate MyopathyReads 1 of these genesORAI1About this report →
- Primary Mitochondrial DiseaseReads 8 of these genesAIFM1AARS2ACAD9AGKCOA8POLGAbout this report →
- Charcot-Marie-Tooth DiseaseReads 6 of these genesVCPAIFM1DCTN1FIG4NEFHMORC2About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 4 of these genesSCN4ACOL6A3PNKDPRRT2About this report →
- Ehlers-Danlos SyndromeReads 3 of these genesDSECOL12A1PLOD1About this report →
- Neurodegeneration with Brain Iron Accumulation (NBIA)Reads 2 of these genesATP13A2PLA2G6About this report →
- Urinary and Renal System TumourReads 2 of these genesSDHASDHBAbout this report →
- Familial Periodic ParalysisReads 1 of these genesSCN4AAbout this report →
- Thyroid Hormone Resistance, Transport & Metabolism DefectsReads 1 of these genesSLC16A2About this report →
- Spinal Muscular AtrophyReads 3 of these genesCHCHD10DCTN1UBA1About this report →
- Parkinson DiseaseReads 2 of these genesATP13A2PLA2G6About this report →
- Hypertrophic CardiomyopathyReads 4 of these genesMYL2HADHALDB3MYH7About this report →
- Adult-Onset Leukodystrophies (CSF1R, LMNB1, Nasu-Hakola)Reads 1 of these genesTREM2About this report →
- Familial Paget Disease of BoneReads 1 of these genesSQSTM1About this report →
- Hereditary Gastrointestinal Stromal TumourReads 1 of these genesSDHBAbout this report →
- Alzheimer diseaseReads 1 of these genesTREM2About this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 2 of these genesSPTLC1AIFM1About this report →
- Vanishing White Matter DiseaseReads 1 of these genesAARS2About this report →
- GlaucomaReads 1 of these genesOPTNAbout this report →
- Hereditary Rickets (Hypophosphatemic and Vitamin D-Dependent)Reads 1 of these genesFGF23About this report →
- Kidney CancerReads 1 of these genesSDHBAbout this report →
- Familial HypomagnesemiaReads 1 of these genesFXYD2About this report →
- LipodystrophyReads 1 of these genesCAVIN1About this report →
- Neuronal Ceroid LipofuscinosisReads 1 of these genesATP13A2About this report →
- Leigh SyndromeReads 2 of these genesAIFM1SDHAAbout this report →
- Epidermolysis BullosaReads 1 of these genesPLECAbout this report →
- Other Inherited LeukodystrophiesReads 2 of these genesTREM2AARS2About this report →
- GPI Anchor Biosynthesis DefectsReads 1 of these genesPIGNAbout this report →
- Pontocerebellar Hypoplasia (TSEN54 and MINPP1)Reads 1 of these genesEXOSC9About this report →
- Syndromic CraniosynostosisReads 1 of these genesRNU12About this report →
- Nephrotic SyndromeReads 1 of these genesLAMB2About this report →
- Thyroid CancerReads 1 of these genesMEN1About this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 1 of these genesATXN2About this report →
- Female InfertilityReads 1 of these genesTWNKAbout this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesTWNKAbout this report →
- Intellectual DisabilityReads 2 of these genesERBB4SLC16A2About this report →
- Lysosomal Storage DiseaseReads 1 of these genesGAAAbout this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesATP13A2About this report →
- Retinitis PigmentosaReads 1 of these genesPOMGNT1About this report →
- Hearing Loss and DeafnessReads 1 of these genesAIFM1About this report →
- Epilepsy (Full Panel)Reads 1 of these genesPRRT2About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesORAI1About this report →
Odczytaj geny powiązane z Generalized muscle weakness oraz resztę swojego genomu za pomocą jednego badania.
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Zamawiam Genome Test122 genów powiązanych z Generalized muscle weakness
Zmiany w tych genach powodują rzadkie choroby, w których występuje Generalized muscle weakness. Większość osób z tą cechą nie ma żadnej z tych chorób, a gen z tej listy nic nie mówi o czyimkolwiek własnym genomie.
| Gen | Jak często występuje | Choroby |
|---|---|---|
| ACTA1actin alpha 1, skeletal muscle | Zawsze | W 5 chorobach |
| CHRNDcholinergic receptor nicotinic delta subunit | Zawsze | W 1 chorobie |
| DSEdermatan sulfate epimerase | Zawsze | W 1 chorobie |
| FKRPfukutin related protein | Zawsze | W 2 chorobach |
| FKTNfukutin | Zawsze | W 2 chorobach |
| GAAalpha glucosidase | Zawsze | W 2 chorobach |
| LMOD3leiomodin 3 | Zawsze | W 1 chorobie |
| MDGA2MAM domain containing glycosylphosphatidylinositol anchor 2 | Zawsze | W 1 chorobie |
| MEGF10multiple EGF like domains 10 | Zawsze | W 1 chorobie |
| MUSKmuscle associated receptor tyrosine kinase | Zawsze | W 1 chorobie |
| MYL2myosin light chain 2 | Zawsze | W 2 chorobach |
| POMT2protein O-mannosyltransferase 2 | Zawsze | W 1 chorobie |
| RNU12RNA, U12 small nuclear | Zawsze | W 1 chorobie |
| RYR1ryanodine receptor 1 | Zawsze | W 3 chorobach |
| SCN4Asodium voltage-gated channel alpha subunit 4 | Zawsze | W 1 chorobie |
| SPTLC1serine palmitoyltransferase long chain base subunit 1 | Zawsze | W 1 chorobie |
| TTNtitin | Zawsze | W 1 chorobie |
| UNC13Aunc-13 homolog A | Zawsze | W 2 chorobach |
| VCPvalosin containing protein | Zawsze | W 2 chorobach |
| AIFM1apoptosis inducing factor mitochondria associated 1 | Bardzo często (80–99%) | W 1 chorobie |
| ANGangiogenin | Bardzo często (80–99%) | W 1 chorobie |
| ANXA11annexin A11 | Bardzo często (80–99%) | W 1 chorobie |
| ATXN2ataxin 2 | Bardzo często (80–99%) | W 1 chorobie |
| CAPN3calpain 3 | Bardzo często (80–99%) | W 1 chorobie |
| CCNFcyclin F | Bardzo często (80–99%) | W 1 chorobie |
| CFAP410cilia and flagella associated protein 410 | Bardzo często (80–99%) | W 1 chorobie |
| CHCHD10coiled-coil-helix-coiled-coil-helix domain containing 10 | Bardzo często (80–99%) | W 1 chorobie |
| CHMP2Bcharged multivesicular body protein 2B | Bardzo często (80–99%) | W 1 chorobie |
| COL12A1collagen type XII alpha 1 chain | Bardzo często (80–99%) | W 2 chorobach |
| COL13A1collagen type XIII alpha 1 chain | Bardzo często (80–99%) | W 1 chorobie |
| COL6A1collagen type VI alpha 1 chain | Bardzo często (80–99%) | W 1 chorobie |
| COL6A2collagen type VI alpha 2 chain | Bardzo często (80–99%) | W 2 chorobach |
| COL6A3collagen type VI alpha 3 chain | Bardzo często (80–99%) | W 1 chorobie |
| COLQcollagen like tail subunit of asymmetric acetylcholinesterase | Bardzo często (80–99%) | W 2 chorobach |
| DAOD-amino acid oxidase | Bardzo często (80–99%) | W 1 chorobie |
| DCTN1dynactin subunit 1 | Bardzo często (80–99%) | W 1 chorobie |
| DNAJB6DnaJ heat shock protein family (Hsp40) member B6 | Bardzo często (80–99%) | W 1 chorobie |
| ERBB4erb-b2 receptor tyrosine kinase 4 | Bardzo często (80–99%) | W 1 chorobie |
| FIG4FIG4 phosphoinositide 5-phosphatase | Bardzo często (80–99%) | W 1 chorobie |
| FUSFUS RNA binding protein | Bardzo często (80–99%) | W 1 chorobie |
Pokaż jeszcze 82 genów
| Gen | Jak często występuje | Choroby |
|---|---|---|
| GLE1GLE1 RNA export mediator | Bardzo często (80–99%) | W 1 chorobie |
| GLT8D1glycosyltransferase 8 domain containing 1 | Bardzo często (80–99%) | W 1 chorobie |
| HNRNPA1heterogeneous nuclear ribonucleoprotein A1 | Bardzo często (80–99%) | W 1 chorobie |
| KLHL41kelch like family member 41 | Bardzo często (80–99%) | W 1 chorobie |
| LAMB2laminin subunit beta 2 | Bardzo często (80–99%) | W 1 chorobie |
| LRP12LDL receptor related protein 12 | Bardzo często (80–99%) | W 1 chorobie |
| MATR3matrin 3 | Bardzo często (80–99%) | W 1 chorobie |
| NEBnebulin | Bardzo często (80–99%) | W 2 chorobach |
| NEFHneurofilament heavy chain | Bardzo często (80–99%) | W 1 chorobie |
| NEK1NIMA related kinase 1 | Bardzo często (80–99%) | W 1 chorobie |
| OPTNoptineurin | Bardzo często (80–99%) | W 1 chorobie |
| ORAI1ORAI calcium release-activated calcium modulator 1 | Bardzo często (80–99%) | W 1 chorobie |
| PFN1profilin 1 | Bardzo często (80–99%) | W 1 chorobie |
| PRPHperipherin | Bardzo często (80–99%) | W 1 chorobie |
| SOD1superoxide dismutase 1 | Bardzo często (80–99%) | W 1 chorobie |
| SQSTM1sequestosome 1 | Bardzo często (80–99%) | W 1 chorobie |
| TAF15TATA-box binding protein associated factor 15 | Bardzo często (80–99%) | W 1 chorobie |
| TARDBPTAR DNA binding protein | Bardzo często (80–99%) | W 1 chorobie |
| TBK1TANK binding kinase 1 | Bardzo często (80–99%) | W 1 chorobie |
| TPM3tropomyosin 3 | Bardzo często (80–99%) | W 4 chorobach |
| TREM2triggering receptor expressed on myeloid cells 2 | Bardzo często (80–99%) | W 1 chorobie |
| UBQLN2ubiquilin 2 | Bardzo często (80–99%) | W 1 chorobie |
| VAPBVAMP associated protein B and C | Bardzo często (80–99%) | W 1 chorobie |
| AARS2alanyl-tRNA synthetase 2, mitochondrial | Często (30–79%) | W 1 chorobie |
| ACAD9acyl-CoA dehydrogenase family member 9 | Często (30–79%) | W 1 chorobie |
| ACY1aminoacylase 1 | Często (30–79%) | W 1 chorobie |
| ADCY5adenylate cyclase 5 | Często (30–79%) | W 1 chorobie |
| AGKacylglycerol kinase | Często (30–79%) | W 1 chorobie |
| BAG3BAG cochaperone 3 | Często (30–79%) | W 1 chorobie |
| CCND1cyclin D1 | Często (30–79%) | W 1 chorobie |
| CHRNA1cholinergic receptor nicotinic alpha 1 subunit | Często (30–79%) | W 2 chorobach |
| COA8cytochrome c oxidase assembly factor 8 | Często (30–79%) | W 1 chorobie |
| CRPPACDP-L-ribitol pyrophosphorylase A | Często (30–79%) | W 1 chorobie |
| EXOSC9exosome component 9 | Często (30–79%) | W 1 chorobie |
| HTThuntingtin | Często (30–79%) | W 1 chorobie |
| IBA57iron-sulfur cluster assembly factor IBA57 | Często (30–79%) | W 1 chorobie |
| MEN1menin 1 | Często (30–79%) | W 1 chorobie |
| MYL1myosin light chain 1 | Często (30–79%) | W 1 chorobie |
| POMT1protein O-mannosyltransferase 1 | Często (30–79%) | W 1 chorobie |
| RANBP2RAN binding protein 2 | Często (30–79%) | W 1 chorobie |
| SDHAsuccinate dehydrogenase complex flavoprotein subunit A | Często (30–79%) | W 1 chorobie |
| SDHAF1succinate dehydrogenase complex assembly factor 1 | Często (30–79%) | W 1 chorobie |
| SDHBsuccinate dehydrogenase complex iron sulfur subunit B | Często (30–79%) | W 1 chorobie |
| SDHDsuccinate dehydrogenase complex subunit D | Często (30–79%) | W 1 chorobie |
| SLC2A3solute carrier family 2 member 3 | Często (30–79%) | W 1 chorobie |
| YY1YY1 transcription factor | Często (30–79%) | W 1 chorobie |
| ATP13A2ATPase cation transporting 13A2 | Czasami (5–29%) | W 1 chorobie |
| DMDdystrophin | Czasami (5–29%) | W 1 chorobie |
| HACD13-hydroxyacyl-CoA dehydratase 1 | Czasami (5–29%) | W 1 chorobie |
| HADHAhydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha | Czasami (5–29%) | W 2 chorobach |
| HADHBhydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta | Czasami (5–29%) | W 1 chorobie |
| ITGA7integrin subunit alpha 7 | Czasami (5–29%) | W 1 chorobie |
| MAP3K20mitogen-activated protein kinase kinase kinase 20 | Czasami (5–29%) | W 1 chorobie |
| MORC2MORC family CW-type zinc finger 2 | Czasami (5–29%) | W 1 chorobie |
| PIGNphosphatidylinositol glycan anchor biosynthesis class N | Czasami (5–29%) | W 1 chorobie |
| PLECplectin | Czasami (5–29%) | W 2 chorobach |
| PLOD1procollagen-lysine,2-oxoglutarate 5-dioxygenase 1 | Czasami (5–29%) | W 1 chorobie |
| PNKDPNKD metallo-beta-lactamase domain containing | Czasami (5–29%) | W 1 chorobie |
| PRRT2proline rich transmembrane protein 2 | Czasami (5–29%) | W 1 chorobie |
| RAPSNreceptor associated protein of the synapse | Czasami (5–29%) | W 1 chorobie |
| SELENONselenoprotein N | Czasami (5–29%) | W 2 chorobach |
| SLC16A2solute carrier family 16 member 2 | Czasami (5–29%) | W 1 chorobie |
| SLC52A3solute carrier family 52 member 3 | Czasami (5–29%) | W 1 chorobie |
| TPM2tropomyosin 2 | Czasami (5–29%) | W 1 chorobie |
| UBA1ubiquitin like modifier activating enzyme 1 | Czasami (5–29%) | W 1 chorobie |
| LDB3LIM domain binding 3 | Rzadko (1–4%) | W 1 chorobie |
| ABCB6ATP binding cassette subfamily B member 6 (LAN blood group) | Nie odnotowano | W 1 chorobie |
| CAVIN1caveolae associated protein 1 | Nie odnotowano | W 1 chorobie |
| CLCNKBchloride voltage-gated channel Kb | Nie odnotowano | W 1 chorobie |
| FGF23fibroblast growth factor 23 | Nie odnotowano | W 1 chorobie |
| FXYD2FXYD domain containing ion transport regulator 2 | Nie odnotowano | W 1 chorobie |
| KCNJ1potassium inwardly rectifying channel subfamily J member 1 | Nie odnotowano | W 1 chorobie |
| MTM1myotubularin 1 | Nie odnotowano | W 1 chorobie |
| MYH2myosin heavy chain 2 | Nie odnotowano | W 1 chorobie |
| MYH7myosin heavy chain 7 | Nie odnotowano | W 1 chorobie |
| PLA2G6phospholipase A2 group VI | Nie odnotowano | W 1 chorobie |
| POLGDNA polymerase gamma, catalytic subunit | Nie odnotowano | W 2 chorobach |
| POMGNT1protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) | Nie odnotowano | W 1 chorobie |
| SLC12A1solute carrier family 12 member 1 | Nie odnotowano | W 1 chorobie |
| SLC12A3solute carrier family 12 member 3 | Nie odnotowano | W 1 chorobie |
| SLC25A4solute carrier family 25 member 4 | Nie odnotowano | W 1 chorobie |
| TWNKtwinkle mtDNA helicase | Nie odnotowano | W 1 chorobie |
Jak często występuje wśród osób z jedną z chorób związanych z tym genem, najczęściej spośród wszystkich, według danych Human Phenotype Ontology. Te strony opisują cechy i badania, na których się opierają; nie są diagnozą, a w sprawie objawów należy zwrócić się do lekarza lub doradcy genetycznego.
Cechy nadrzędne
Skąd pochodzą te dane
- Human Phenotype Ontology, wydanie 2026-09-01: cecha, jej nazwy, definicja oraz geny z nią powiązane. Więcej informacji znajdą Państwo na stronie hpo.jax.org.
- Wydanie danych 2026.10.21-777c9289.
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Read the genes behind these traits in your own DNA.
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