Kenmerk
Tetraparesis
Weakness of all four limbs.
Samenvatting
- Ook bekend als
- Quadriparesis
- Lichaamssysteem
- Abnormality of the nervous system
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page$trait$nameLees de genen die aan Tetraparesis gekoppeld zijn, en de rest van uw genoom, met één test.
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Mijn 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.
- Hereditary Episodic AtaxiasReads 3 of these genesCACNA1ASCN2ASLC1A3About this report →
- Frontotemporal DementiaReads 5 of these genesVCPCHCHD10SQSTM1TBK1C9orf72About this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 7 of these genesVCPCHCHD10FUSSQSTM1TARDBPTBK1About this report →
- Familial Hemiplegic MigraineReads 2 of these genesATP1A2CACNA1AAbout this report →
Show 52 more reports
- Inherited Neurodegenerative DisordersReads 21 of these genesDNM1LVCPADARAGTPBP1ATP1A3CACNA1AAbout this report →
- Familial Paget Disease of BoneReads 2 of these genesSQSTM1TNFRSF11AAbout this report →
- Amyotrophic Lateral Sclerosis Susceptibility 24 (NEK1)Reads 1 of these genesNEK1About this report →
- ATP1A2-Related Fetal Akinesia with PolymicrogyriaReads 1 of these genesATP1A2About this report →
- Cenani-Lenz Syndactyly SyndromeReads 1 of these genesLRP4About this report →
- COL4A1-Related DisorderReads 1 of these genesCOL4A1About this report →
- Dyschromatosis Symmetrica HereditariaReads 1 of these genesADARAbout this report →
- Jaberi-Elahi SyndromeReads 1 of these genesGTPBP2About this report →
- Krabbe DiseaseReads 1 of these genesGALCAbout this report →
- Primary Microcephaly 26 (LMNB1)Reads 1 of these genesLMNB1About this report →
- Purine Nucleoside Phosphorylase DeficiencyReads 1 of these genesPNPAbout this report →
- UNC13A-Related Neurodevelopmental DisordersReads 1 of these genesUNC13AAbout this report →
- Epilepsy (Full Panel)Reads 11 of these genesTMEM63BNEXMIFATP1A2ATP1A3CACNA1ARHOBTB2About this report →
- Rare Hereditary Peripheral NeuropathiesReads 11 of these genesAIFM1VCPCHCHD10MT-ATP6PDHXPOLGAbout this report →
- Aicardi-Goutieres SyndromeReads 2 of these genesADARIFIH1About this report →
- Encephalopathy due to Mitochondrial and Peroxisomal Fission DefectReads 1 of these genesDNM1LAbout this report →
- Leigh SyndromeReads 5 of these genesAIFM1MT-ATP6PDHXSLC19A3NDUFS3About this report →
- Other Inherited LeukodystrophiesReads 5 of these genesADARPOLR3KIFIH1LMNB1GALCAbout this report →
- Hereditary Optic NeuropathyReads 2 of these genesDNM1LATP1A3About this report →
- OsteopetrosisReads 2 of these genesCA2TNFRSF11AAbout this report →
- Adult-Onset Leukodystrophies (CSF1R, LMNB1, Nasu-Hakola)Reads 1 of these genesLMNB1About this report →
- Thiamine Transporter and Metabolism DisordersReads 1 of these genesSLC19A3About this report →
- Charcot-Marie-Tooth DiseaseReads 4 of these genesAIFM1VCPBSCL2HINT1About this report →
- Periventricular Nodular HeterotopiaReads 1 of these genesARFGEF2About this report →
- Spinal Muscular AtrophyReads 2 of these genesCHCHD10BSCL2About this report →
- Basal Ganglia CalcificationReads 1 of these genesNAA60About this report →
- Hepatic Porphyria DisordersReads 1 of these genesPPOXAbout this report →
- Rare Monogenic Autoinflammatory DiseasesReads 2 of these genesADARIFIH1About this report →
- Primary Mitochondrial DiseaseReads 4 of these genesAIFM1CARS2POLGNDUFS3About this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 2 of these genesATP1A3CACNA1AAbout this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 2 of these genesATP1A3SLC2A1About this report →
- Complex Neurodevelopmental Disorder With Motor FeaturesReads 1 of these genesCACNA1AAbout this report →
- PorphyriaReads 1 of these genesPPOXAbout this report →
- Pyruvate Dehydrogenase & Pyruvate Carboxylase DeficiencyReads 1 of these genesPDHXAbout this report →
- LipodystrophyReads 1 of these genesBSCL2About this report →
- Type I InterferonopathiesReads 1 of these genesIFIH1About this report →
- Complex Cortical Dysplasia and Frontoparietal PolymicrogyriaReads 1 of these genesTUBB2BAbout this report →
- Glycogen Storage DiseaseReads 1 of these genesGBE1About this report →
- Hereditary Spastic ParaplegiaReads 2 of these genesBSCL2UCHL1About this report →
- Distal MyopathiesReads 1 of these genesVCPAbout this report →
- Neonatal Diabetes MellitusReads 1 of these genesBSCL2About this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 1 of these genesAIFM1About this report →
- Leber Congenital Amaurosis & RPE65-Related RetinopathyReads 1 of these genesNMNAT1About this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 1 of these genesPOLR3KAbout this report →
- Congenital Myasthenic SyndromeReads 1 of these genesLRP4About this report →
- Diabetes MellitusReads 1 of these genesBSCL2About this report →
- Osteogenesis ImperfectaReads 1 of these genesIFIH1About this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 1 of these genesGJA1About this report →
- Other Inborn Errors of ImmunityReads 2 of these genesADARIFIH1About this report →
- Intellectual DisabilityReads 2 of these genesNEXMIFSCN2AAbout this report →
- Lysosomal Storage DiseaseReads 1 of these genesGALCAbout this report →
- Hearing Loss and DeafnessReads 1 of these genesAIFM1About this report →
Lees de genen die aan Tetraparesis gekoppeld zijn, en de rest van uw genoom, met één test.
Vanaf $ 449Gratis verzending · Resultaten binnen 6–8 weken
Mijn Genome Test bestellen64 genen gekoppeld aan Tetraparesis
Veranderingen in deze genen veroorzaken zeldzame aandoeningen waarbij Tetraparesis 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 |
|---|---|---|
| AIFM1apoptosis inducing factor mitochondria associated 1 | Altijd | In 1 aandoening |
| CARS2cysteinyl-tRNA synthetase 2, mitochondrial | Altijd | In 2 aandoeningen |
| COL4A2collagen type IV alpha 2 chain | Altijd | In 1 aandoening |
| DNM1Ldynamin 1L | Altijd | In 1 aandoening |
| GTF3C3general transcription factor IIIC subunit 3 | Altijd | In 1 aandoening |
| GTPBP1GTP binding protein 1 | Altijd | In 1 aandoening |
| LSM7LSM7 homolog, U6 small nuclear RNA and mRNA degradation associated | Altijd | In 1 aandoening |
| PTPMT1protein tyrosine phosphatase mitochondrial 1 | Altijd | In 1 aandoening |
| RRP12ribosomal RNA processing 12 homolog | Altijd | In 1 aandoening |
| SLC25A10solute carrier family 25 member 10 | Altijd | In 1 aandoening |
| TMEM63Btransmembrane protein 63B | Altijd | In 1 aandoening |
| VCPvalosin containing protein | Altijd | In 3 aandoeningen |
| GTPBP2GTP binding protein 2 | Heel vaak (80–99%) | In 1 aandoening |
| NEXMIFneurite extension and migration factor | Heel vaak (80–99%) | In 1 aandoening |
| ADARadenosine deaminase RNA specific | Vaak (30–79%) | In 1 aandoening |
| AGTPBP1ATP/GTP binding carboxypeptidase 1 | Vaak (30–79%) | In 1 aandoening |
| ATP1A2ATPase Na+/K+ transporting subunit alpha 2 | Vaak (30–79%) | In 1 aandoening |
| ATP1A3ATPase Na+/K+ transporting subunit alpha 3 | Vaak (30–79%) | In 1 aandoening |
| CACNA1Acalcium voltage-gated channel subunit alpha1 A | Vaak (30–79%) | In 1 aandoening |
| CHCHD10coiled-coil-helix-coiled-coil-helix domain containing 10 | Vaak (30–79%) | In 1 aandoening |
| FUSFUS RNA binding protein | Vaak (30–79%) | In 1 aandoening |
| MT-ATP6mitochondrially encoded ATP synthase membrane subunit 6 | Vaak (30–79%) | In 1 aandoening |
| MT-TL2mitochondrially encoded tRNA-Leu (CUN) 2 | Vaak (30–79%) | In 1 aandoening |
| NAXENAD(P)HX epimerase | Vaak (30–79%) | In 1 aandoening |
| NEK1NIMA related kinase 1 | Vaak (30–79%) | In 1 aandoening |
| NMNAT1nicotinamide nucleotide adenylyltransferase 1 | Vaak (30–79%) | In 1 aandoening |
| NUP54nucleoporin 54 | Vaak (30–79%) | In 1 aandoening |
| NUP62nucleoporin 62 | Vaak (30–79%) | In 1 aandoening |
| PDHXpyruvate dehydrogenase complex component X | Vaak (30–79%) | In 1 aandoening |
| POLGDNA polymerase gamma, catalytic subunit | Vaak (30–79%) | In 1 aandoening |
| POLR3KRNA polymerase III subunit K | Vaak (30–79%) | In 1 aandoening |
| PPOXprotoporphyrinogen oxidase | Vaak (30–79%) | In 1 aandoening |
| RHOBTB2Rho related BTB domain containing 2 | Vaak (30–79%) | In 1 aandoening |
| SCN2Asodium voltage-gated channel alpha subunit 2 | Vaak (30–79%) | In 1 aandoening |
| SLC19A3solute carrier family 19 member 3 | Vaak (30–79%) | In 2 aandoeningen |
| SLC1A2solute carrier family 1 member 2 | Vaak (30–79%) | In 1 aandoening |
| SLC1A3solute carrier family 1 member 3 | Vaak (30–79%) | In 1 aandoening |
| SLC2A1solute carrier family 2 member 1 | Vaak (30–79%) | In 1 aandoening |
| SQSTM1sequestosome 1 | Vaak (30–79%) | In 1 aandoening |
| TARDBPTAR DNA binding protein | Vaak (30–79%) | In 1 aandoening |
Toon nog 24 genen
| Gen | Hoe vaak het voorkomt | Aandoeningen |
|---|---|---|
| TBK1TANK binding kinase 1 | Vaak (30–79%) | In 1 aandoening |
| TUBB2Btubulin beta 2B class IIb | Vaak (30–79%) | In 1 aandoening |
| UNC13Aunc-13 homolog A | Vaak (30–79%) | In 1 aandoening |
| BSCL2BSCL2 lipid droplet biogenesis associated, seipin | Soms (5–29%) | In 2 aandoeningen |
| GAD1glutamate decarboxylase 1 | Soms (5–29%) | In 1 aandoening |
| HINT1histidine triad nucleotide binding protein 1 | Soms (5–29%) | In 1 aandoening |
| IFIH1interferon induced with helicase C domain 1 | Soms (5–29%) | In 1 aandoening |
| LMNB1lamin B1 | Soms (5–29%) | In 1 aandoening |
| NAA60N-alpha-acetyltransferase 60, NatF catalytic subunit | Soms (5–29%) | In 1 aandoening |
| SARDHsarcosine dehydrogenase | Soms (5–29%) | In 1 aandoening |
| UGP2UDP-glucose pyrophosphorylase 2 | Soms (5–29%) | In 1 aandoening |
| CA2carbonic anhydrase 2 | Zelden (1–4%) | In 1 aandoening |
| GALCgalactosylceramidase | Zelden (1–4%) | In 1 aandoening |
| ARFGEF2ARF guanine nucleotide exchange factor 2 | Niet vastgelegd | In 1 aandoening |
| C9orf72C9orf72-SMCR8 complex subunit | Niet vastgelegd | In 1 aandoening |
| COL4A1collagen type IV alpha 1 chain | Niet vastgelegd | In 1 aandoening |
| GBE11,4-alpha-glucan branching enzyme 1 | Niet vastgelegd | In 1 aandoening |
| GJA1gap junction protein alpha 1 | Niet vastgelegd | In 1 aandoening |
| LIMS2LIM zinc finger domain containing 2 | Niet vastgelegd | In 1 aandoening |
| LRP4LDL receptor related protein 4 | Niet vastgelegd | In 1 aandoening |
| NDUFS3NADH:ubiquinone oxidoreductase core subunit S3 | Niet vastgelegd | In 1 aandoening |
| PNPpurine nucleoside phosphorylase | Niet vastgelegd | In 1 aandoening |
| TNFRSF11ATNF receptor superfamily member 11a | Niet vastgelegd | In 1 aandoening |
| UCHL1ubiquitin C-terminal hydrolase L1 | 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.
Smallere kenmerken
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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