Merkmal
Limb muscle weakness
Reduced strength and weakness of the muscles of the arms and legs.
Zusammenfassung
- Auch genannt
- Limb weakness
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page$trait$nameLesen Sie die Gene aus, die mit Limb muscle weakness zusammenhängen, und den Rest Ihres Genoms, mit einem einzigen Test.
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Meinen Genome Test bestellen56 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.
- Congenital MyopathiesReads 8 of these genesCFL2ACTA1KBTBD13KLHL41MYPNNEBAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 18 of these genesPMP22SDHARRM2BPOLGBTDGANAbout this report →
- Charcot-Marie-Tooth DiseaseReads 10 of these genesPMP22VCPDYNC1H1GDAP1IGHMBP2LMNAAbout this report →
- Alexander DiseaseReads 1 of these genesGFAPAbout this report →
Show 52 more reports
- Androgen Insensitivity SyndromeReads 1 of these genesARAbout this report →
- Danon DiseaseReads 1 of these genesLAMP2About this report →
- Hereditary Neuropathy with Liability to Pressure Palsies (HNPP)Reads 1 of these genesPMP22About this report →
- MEGF10-Related MyopathyReads 1 of these genesMEGF10About this report →
- Mitchell SyndromeReads 1 of these genesACOX1About this report →
- Pompe DiseaseReads 1 of these genesGAAAbout this report →
- SCN4A-Related Congenital MyopathyReads 1 of these genesSCN4AAbout this report →
- Spinal and Bulbar Muscular Atrophy (Kennedy Disease)Reads 1 of these genesARAbout this report →
- Wilson DiseaseReads 1 of these genesATP7BAbout this report →
- Congenital Myasthenic SyndromeReads 5 of these genesCHRNA1CHRNB1SCN4ACOLQCHRNEAbout this report →
- Inherited Neurodegenerative DisordersReads 18 of these genesCOA7HNRNPA2B1SDHATBCKGFAPPOLGAbout this report →
- Frontotemporal DementiaReads 3 of these genesHNRNPA2B1VCPCCNFAbout this report →
- Peroxisomal Enzyme Disorders & Refsum DiseaseReads 2 of these genesACOX1PHYHAbout this report →
- Biotinidase & Holocarboxylase DeficiencyReads 1 of these genesBTDAbout this report →
- Fontaine Progeroid SyndromeReads 1 of these genesSLC25A4About this report →
- Riboflavin Transporter DeficiencyReads 1 of these genesSLC52A2About this report →
- Distal MyopathiesReads 3 of these genesHNRNPA2B1TIA1VCPAbout this report →
- Primary Mitochondrial DiseaseReads 8 of these genesGUK1RNASEH1RRM2BPOLGPOLG2SLC25A4About this report →
- LipodystrophyReads 2 of these genesLMNAMFN2About this report →
- Disorder of Copper MetabolismReads 1 of these genesATP7BAbout this report →
- Familial Periodic ParalysisReads 1 of these genesSCN4AAbout this report →
- Neuroacanthocytosis and Huntington Disease PhenocopiesReads 1 of these genesVPS13AAbout this report →
- Sclerosing Bone Dysplasias (High Bone Mass)Reads 1 of these genesMTAPAbout this report →
- Syndromic and Metabolic CardiomyopathiesReads 1 of these genesSLC25A4About this report →
- Spinal Muscular AtrophyReads 2 of these genesDYNC1H1IGHMBP2About this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 2 of these genesVCPCCNFAbout this report →
- Hepatic Porphyria DisordersReads 1 of these genesALADAbout this report →
- Malignant Endocrine NeoplasmReads 1 of these genesSDHAAbout this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesLMNAAbout this report →
- Limb-Girdle Muscular DystrophyReads 2 of these genesPOPDC1LMNAAbout this report →
- PorphyriaReads 1 of these genesALADAbout this report →
- Hereditary Pheochromocytoma and ParagangliomaReads 1 of these genesSDHAAbout this report →
- Urinary and Renal System TumourReads 1 of these genesSDHAAbout this report →
- Dilated CardiomyopathyReads 2 of these genesMYPNLMNAAbout this report →
- Myofibrillar MyopathiesReads 1 of these genesPYROXD1About this report →
- Zellweger Spectrum & Peroxisome Biogenesis DisordersReads 1 of these genesPEX7About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 2 of these genesCOA7TWNKAbout this report →
- Lysosomal Storage DiseaseReads 2 of these genesGAALAMP2About this report →
- Complex Cortical Dysplasia and Frontoparietal PolymicrogyriaReads 1 of these genesDYNC1H1About this report →
- Leigh SyndromeReads 2 of these genesSDHABTDAbout this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 1 of these genesARAbout this report →
- Other Inherited LeukodystrophiesReads 2 of these genesGFAPPEX7About this report →
- Ehlers-Danlos SyndromeReads 1 of these genesPLOD1About this report →
- Syndromic Complex Neurodevelopmental DisorderReads 1 of these genesTBCKAbout this report →
- VitreoretinopathyReads 1 of these genesDYNC1H1About this report →
- Congenital Muscular DystrophiesReads 1 of these genesTRIP4About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesSCN4AAbout this report →
- DNA Repair DiseaseReads 1 of these genesCOA7About this report →
- Female InfertilityReads 1 of these genesTWNKAbout this report →
- Hypertrophic CardiomyopathyReads 1 of these genesMYPNAbout this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesGBA2About this report →
- Intellectual DisabilityReads 1 of these genesDYNC1H1About this report →
Lesen Sie die Gene aus, die mit Limb muscle weakness zusammenhängen, und den Rest Ihres Genoms, mit einem einzigen Test.
Ab 449 $Kostenloser Versand · Ergebnisse in 6–8 Wochen
Meinen Genome Test bestellen66 Gene mit Limb muscle weakness verknüpft
Veränderungen in diesen Genen verursachen seltene Erkrankungen, bei denen Limb muscle weakness auftritt. Die meisten Menschen mit diesem Merkmal haben keine dieser Erkrankungen, und ein Gen auf dieser Liste sagt nichts über das eigene Genom einer Person aus.
| Gen | Wie häufig es auftritt | Erkrankungen |
|---|---|---|
| ATP7BATPase copper transporting beta | Immer | In 1 Erkrankung |
| CFL2cofilin 2 | Immer | In 1 Erkrankung |
| CHRNA1cholinergic receptor nicotinic alpha 1 subunit | Immer | In 1 Erkrankung |
| CHRNB1cholinergic receptor nicotinic beta 1 subunit | Immer | In 1 Erkrankung |
| COA7cytochrome c oxidase assembly factor 7 | Immer | In 1 Erkrankung |
| GAAalpha glucosidase | Immer | In 1 Erkrankung |
| GUK1guanylate kinase 1 | Immer | In 1 Erkrankung |
| HNRNPA2B1heterogeneous nuclear ribonucleoprotein A2/B1 | Immer | In 1 Erkrankung |
| MEGF10multiple EGF like domains 10 | Immer | In 1 Erkrankung |
| NOTCH2NLCnotch 2 N-terminal like C | Immer | In 1 Erkrankung |
| PMP22peripheral myelin protein 22 | Immer | In 2 Erkrankungen |
| PYROXD1pyridine nucleotide-disulphide oxidoreductase domain 1 | Immer | In 1 Erkrankung |
| RFC4replication factor C subunit 4 | Immer | In 1 Erkrankung |
| SCN4Asodium voltage-gated channel alpha subunit 4 | Immer | In 2 Erkrankungen |
| SDHAsuccinate dehydrogenase complex flavoprotein subunit A | Immer | In 1 Erkrankung |
| TBCKTBC1 domain containing kinase | Immer | In 1 Erkrankung |
| AMPD1adenosine monophosphate deaminase 1 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| AMPD3adenosine monophosphate deaminase 3 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| RNASEH1ribonuclease H1 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| RRM1ribonucleotide reductase catalytic subunit M1 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| ACTA1actin alpha 1, skeletal muscle | Häufig (30–79 %) | In 2 Erkrankungen |
| DYMdymeclin | Häufig (30–79 %) | In 1 Erkrankung |
| GFAPglial fibrillary acidic protein | Häufig (30–79 %) | In 1 Erkrankung |
| KBTBD13kelch repeat and BTB domain containing 13 | Häufig (30–79 %) | In 2 Erkrankungen |
| KLHL41kelch like family member 41 | Häufig (30–79 %) | In 1 Erkrankung |
| LAMP2lysosome associated membrane protein 2 | Häufig (30–79 %) | In 1 Erkrankung |
| MYPNmyopalladin | Häufig (30–79 %) | In 1 Erkrankung |
| NEBnebulin | Häufig (30–79 %) | In 2 Erkrankungen |
| POLGDNA polymerase gamma, catalytic subunit | Häufig (30–79 %) | In 2 Erkrankungen |
| POLG2DNA polymerase gamma 2, accessory subunit | Häufig (30–79 %) | In 2 Erkrankungen |
| POPDC1popeye domain cAMP effector 1 | Häufig (30–79 %) | In 1 Erkrankung |
| SLC25A4solute carrier family 25 member 4 | Häufig (30–79 %) | In 1 Erkrankung |
| TPM2tropomyosin 2 | Häufig (30–79 %) | In 2 Erkrankungen |
| TPM3tropomyosin 3 | Häufig (30–79 %) | In 1 Erkrankung |
| TRIP4thyroid hormone receptor interactor 4 | Häufig (30–79 %) | In 1 Erkrankung |
| TWNKtwinkle mtDNA helicase | Häufig (30–79 %) | In 2 Erkrankungen |
| ALADaminolevulinate dehydratase | Manchmal (5–29 %) | In 1 Erkrankung |
| BTDbiotinidase | Manchmal (5–29 %) | In 1 Erkrankung |
| COLQcollagen like tail subunit of asymmetric acetylcholinesterase | Manchmal (5–29 %) | In 1 Erkrankung |
26 weitere Gene anzeigen
| Gen | Wie häufig es auftritt | Erkrankungen |
|---|---|---|
| GANgigaxonin | Manchmal (5–29 %) | In 1 Erkrankung |
| PLOD1procollagen-lysine,2-oxoglutarate 5-dioxygenase 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| TIA1TIA1 cytotoxic granule associated RNA binding protein | Manchmal (5–29 %) | In 1 Erkrankung |
| VCPvalosin containing protein | Manchmal (5–29 %) | In 2 Erkrankungen |
| ACOX1acyl-CoA oxidase 1 | Nicht erfasst | In 1 Erkrankung |
| ARandrogen receptor | Nicht erfasst | In 1 Erkrankung |
| CCNFcyclin F | Nicht erfasst | In 1 Erkrankung |
| CD59CD59 molecule (CD59 blood group) | Nicht erfasst | In 1 Erkrankung |
| CHRNEcholinergic receptor nicotinic epsilon subunit | Nicht erfasst | In 1 Erkrankung |
| DYNC1H1dynein cytoplasmic 1 heavy chain 1 | Nicht erfasst | In 1 Erkrankung |
| GBA2glucosylceramidase beta 2 | Nicht erfasst | In 1 Erkrankung |
| GDAP1ganglioside induced differentiation associated protein 1 | Nicht erfasst | In 1 Erkrankung |
| IGHMBP2immunoglobulin mu DNA binding protein 2 | Nicht erfasst | In 1 Erkrankung |
| KIF1Bkinesin family member 1B | Nicht erfasst | In 1 Erkrankung |
| LMNAlamin A/C | Nicht erfasst | In 1 Erkrankung |
| MFN2mitofusin 2 | Nicht erfasst | In 2 Erkrankungen |
| MPZmyelin protein zero | Nicht erfasst | In 1 Erkrankung |
| MTAPmethylthioadenosine phosphorylase | Nicht erfasst | In 1 Erkrankung |
| PABPN1poly(A) binding protein nuclear 1 | Nicht erfasst | In 1 Erkrankung |
| PEX7peroxisomal biogenesis factor 7 | Nicht erfasst | In 1 Erkrankung |
| PHYHphytanoyl-CoA 2-hydroxylase | Nicht erfasst | In 1 Erkrankung |
| PRXperiaxin | Nicht erfasst | In 1 Erkrankung |
| SLC12A6solute carrier family 12 member 6 | Nicht erfasst | In 1 Erkrankung |
| SLC52A2solute carrier family 52 member 2 | Nicht erfasst | In 1 Erkrankung |
| TK2thymidine kinase 2 | Nicht erfasst | In 1 Erkrankung |
| VPS13Avacuolar protein sorting 13 homolog A | Nicht erfasst | In 1 Erkrankung |
Wie häufig dieses Merkmal bei Menschen mit einer der Erkrankungen auftritt, die mit dem Gen in Verbindung stehen, und zwar der höchste Wert unter ihnen, so wie ihn die Human Phenotype Ontology erfasst. Diese Seiten beschreiben Merkmale und die dazugehörige Forschung; sie stellen keine Diagnose dar. Fragen zu Symptomen richten Sie bitte an Ihre Ärztin, Ihren Arzt oder eine genetische Beratung.
Untergeordnete Merkmale
Übergeordnete Merkmale
Woher diese Angaben stammen
- Die Human Phenotype Ontology, Version 2026-09-01: das Merkmal, seine Bezeichnungen, seine Definition und die damit verknüpften Gene. Weitere Informationen finden Sie unter hpo.jax.org.
- Datenstand 2026.10.19-9814e911.
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