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Egenskap
Overactive lower leg reflex
Kliniskt namn: Lower limb hyperreflexia
Increased intensity of the a reflex in the leg.
Sammanfattning
- Även kallad
- Brisk lower extremity reflexes, Hyperreflexia in lower limbs, Hyperreflexia in the lower limbs, Increased deep tendon reflexes in the lower limbs, Leg hyperreflexia
- Kroppssystem
- Abnormality of the nervous system
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Den här sidan som data
Lägg till .json i sidans adress, eller begär application/json, för att läsa den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/lower-limb-hyperreflexia.json"
page <- fromJSON(url)
page$trait$nameOveractive lower leg reflexHP:0002395
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Läs generna kopplade till Overactive lower leg reflex, och resten av ditt genom, med ett enda test.
Från 449 $Fri frakt · Resultat inom 6–8 veckor
Beställ mitt Genome Test57 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 Spastic ParaplegiaReads 26 of these genesALDH18A1AMFRCAPN1CYP2U1FARS2HPDLAbout this report →
- Inherited Neurodegenerative DisordersReads 40 of these genesALDH18A1AMFRCAPN1CLDN11CYP2U1FARS2About this report →
- Angelman SyndromeReads 1 of these genesUBE3AAbout this report →
- Basilicata-Akhtar SyndromeReads 1 of these genesMSL3About this report →
Show 53 more reports
- EBF3-Related Neurodevelopmental Disorder (HADDS)Reads 1 of these genesEBF3About this report →
- GTP Cyclohydrolase 1 DeficiencyReads 1 of these genesGCH1About this report →
- KIF5A-Related Amyotrophic Lateral SclerosisReads 1 of these genesKIF5AAbout this report →
- P5CS Deficiency (ALDH18A1-Related)Reads 1 of these genesALDH18A1About this report →
- Rett Syndrome and MECP2-Related DisordersReads 1 of these genesMECP2About this report →
- TNR-Related Neurodevelopmental Disorder with SpasticityReads 1 of these genesTNRAbout this report →
- VPS11-Related LeukodystrophyReads 1 of these genesVPS11About this report →
- Alzheimer diseaseReads 2 of these genesAPOEPSEN1About this report →
- Rare Hereditary Peripheral NeuropathiesReads 13 of these genesFARS2HPDLKIF1ARTN2VCPATL1About this report →
- Cantú SyndromeReads 1 of these genesABCC9About this report →
- Cerebral Arteriopathy with Subcortical Infarcts and LeukoencephalopathyReads 1 of these genesNOTCH3About this report →
- Charcot-Marie-Tooth DiseaseReads 6 of these genesRTN2VCPSPG11REEP1GJB1SPTAN1About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 4 of these genesGCH1NR4A2TSPOAP1TAF1About this report →
- Neurodegeneration with Brain Iron Accumulation (NBIA)Reads 2 of these genesATP13A2FTLAbout this report →
- BH4 Deficiency & Monoamine Neurotransmitter DisordersReads 2 of these genesGCH1THAbout this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 3 of these genesCLDN11VPS11RARS1About this report →
- Frontotemporal DementiaReads 2 of these genesVCPPSEN1About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 4 of these genesVLDLRMKS1RUBCNSYNE1About this report →
- Carney Complex & Hereditary Adrenal Cushing SyndromeReads 1 of these genesPDE8BAbout this report →
- Complex Neurodevelopmental Disorder (TRRAP, MYH10, RERE, SOX11)Reads 1 of these genesTRRAPAbout this report →
- Leigh SyndromeReads 4 of these genesFARS2HPDLDLATMTRFRAbout this report →
- Other Inherited LeukodystrophiesReads 4 of these genesCLDN11VPS11RARS1TREX1About this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 2 of these genesKIF1AATL1About this report →
- Systemic Lupus ErythematosusReads 1 of these genesTREX1About this report →
- Spinal Muscular AtrophyReads 2 of these genesREEP1SPTAN1About this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 2 of these genesVCPSPG11About this report →
- Epilepsy (Full Panel)Reads 5 of these genesGLULMECP2RUBCNSPTAN1KDM5CAbout this report →
- Aicardi-Goutieres SyndromeReads 1 of these genesTREX1About this report →
- Oculocutaneous AlbinismReads 1 of these genesOCA2About this report →
- Primary Mitochondrial DiseaseReads 4 of these genesFARS2AFG3L2COQ4MTRFRAbout this report →
- Pyruvate Dehydrogenase & Pyruvate Carboxylase DeficiencyReads 1 of these genesDLATAbout this report →
- Meckel SyndromeReads 1 of these genesMKS1About this report →
- Type I InterferonopathiesReads 1 of these genesTREX1About this report →
- Dilated CardiomyopathyReads 2 of these genesABCC9SYNE1About this report →
- Hereditary Optic NeuropathyReads 1 of these genesAFG3L2About this report →
- HyperlipidemiaReads 1 of these genesAPOEAbout this report →
- Myofibrillar MyopathiesReads 1 of these genesKYAbout this report →
- Neuronal Ceroid LipofuscinosisReads 1 of these genesATP13A2About this report →
- Intellectual DisabilityReads 4 of these genesKIF1AMECP2TAF1KDM5CAbout this report →
- Parkinson DiseaseReads 1 of these genesATP13A2About this report →
- Cutis LaxaReads 1 of these genesALDH18A1About this report →
- Distal MyopathiesReads 1 of these genesVCPAbout this report →
- GPI Anchor Biosynthesis DefectsReads 1 of these genesST3GAL5About this report →
- Autoimmune DiseaseReads 1 of these genesTREX1About this report →
- Bardet-Biedl and Alström SyndromesReads 1 of these genesMKS1About this report →
- Hereditary Congenital & Juvenile CataractReads 1 of these genesFTLAbout this report →
- Congenital Disorders of GlycosylationReads 2 of these genesDPM1ST3GAL5About this report →
- Congenital Muscular DystrophiesReads 1 of these genesLARGE1About this report →
- Rare Monogenic Autoinflammatory DiseasesReads 1 of these genesTREX1About this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 1 of these genesAFG3L2About this report →
- Joubert Syndrome And Related DisordersReads 1 of these genesMKS1About this report →
- Lysosomal Storage DiseaseReads 1 of these genesSUMF1About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesTREX1About this report →
Läs generna kopplade till Overactive lower leg reflex, och resten av ditt genom, med ett enda test.
Från 449 $Fri frakt · Resultat inom 6–8 veckor
Beställ mitt Genome Test79 gener kopplade till Overactive lower leg reflex
Förändringar i dessa gener orsakar sällsynta tillstånd där Overactive lower leg reflex förekommer. De flesta med denna egenskap har inget av dessa tillstånd, och en gen på listan säger ingenting om någons eget genom.
| Gen | Hur ofta den förekommer | Tillstånd |
|---|---|---|
| ALDH18A1aldehyde dehydrogenase 18 family member A1 | Alltid | I 4 tillstånd |
| AMFRautocrine motility factor receptor | Alltid | I 1 tillstånd |
| CAPN1calpain 1 | Alltid | I 2 tillstånd |
| CLDN11claudin 11 | Alltid | I 1 tillstånd |
| CYP2U1cytochrome P450 family 2 subfamily U member 1 | Alltid | I 2 tillstånd |
| FARS2phenylalanyl-tRNA synthetase 2, mitochondrial | Alltid | I 2 tillstånd |
| GLULglutamate-ammonia ligase | Alltid | I 1 tillstånd |
| HPDL4-hydroxyphenylpyruvate dioxygenase like | Alltid | I 1 tillstånd |
| KIF1Akinesin family member 1A | Alltid | I 2 tillstånd |
| KLC4kinesin light chain 4 | Alltid | I 1 tillstånd |
| KPNA3karyopherin subunit alpha 3 | Alltid | I 1 tillstånd |
| LARGE1LARGE xylosyl- and glucuronyltransferase 1 | Alltid | I 1 tillstånd |
| LBRlamin B receptor | Alltid | I 1 tillstånd |
| NOTCH3notch receptor 3 | Alltid | I 1 tillstånd |
| REEP2receptor accessory protein 2 | Alltid | I 2 tillstånd |
| RTN2reticulon 2 | Alltid | I 1 tillstånd |
| SELENOIselenoprotein I | Alltid | I 1 tillstånd |
| SPG7SPG7 matrix AAA peptidase subunit, paraplegin | Alltid | I 2 tillstånd |
| TMEM63Ctransmembrane protein 63C | Alltid | I 1 tillstånd |
| UBAP1ubiquitin associated protein 1 | Alltid | I 1 tillstånd |
| VCPvalosin containing protein | Alltid | I 1 tillstånd |
| VLDLRvery low density lipoprotein receptor | Alltid | I 1 tillstånd |
| VPS11VPS11 core subunit of CORVET and HOPS complexes | Alltid | I 1 tillstånd |
| WASHC5WASH complex subunit 5 | Alltid | I 1 tillstånd |
| AFG3L2AFG3 like matrix AAA peptidase subunit 2 | Mycket ofta (80–99 %) | I 2 tillstånd |
| ATL1atlastin GTPase 1 | Mycket ofta (80–99 %) | I 1 tillstånd |
| ATP13A2ATPase cation transporting 13A2 | Mycket ofta (80–99 %) | I 1 tillstånd |
| COQ4coenzyme Q4 | Mycket ofta (80–99 %) | I 1 tillstånd |
| ERLIN1ER lipid raft associated 1 | Mycket ofta (80–99 %) | I 1 tillstånd |
| KIF1Ckinesin family member 1C | Mycket ofta (80–99 %) | I 1 tillstånd |
| KIF5Akinesin family member 5A | Mycket ofta (80–99 %) | I 1 tillstånd |
| NIPA1NIPA magnesium transporter 1 | Mycket ofta (80–99 %) | I 1 tillstånd |
| SPG11SPG11 vesicle trafficking associated, spatacsin | Mycket ofta (80–99 %) | I 1 tillstånd |
| TNRtenascin R | Mycket ofta (80–99 %) | I 1 tillstånd |
| ABCC9ATP binding cassette subfamily C member 9 | Ofta (30–79 %) | I 1 tillstånd |
| DKK1dickkopf Wnt signaling pathway inhibitor 1 | Ofta (30–79 %) | I 1 tillstånd |
| DLATdihydrolipoamide S-acetyltransferase | Ofta (30–79 %) | I 1 tillstånd |
| EBF3EBF transcription factor 3 | Ofta (30–79 %) | I 1 tillstånd |
| GCH1GTP cyclohydrolase 1 | Ofta (30–79 %) | I 1 tillstånd |
| IFRD1interferon related developmental regulator 1 | Ofta (30–79 %) | I 1 tillstånd |
Visa 39 gener till
| Gen | Hur ofta den förekommer | Tillstånd |
|---|---|---|
| IMPDH2inosine monophosphate dehydrogenase 2 | Ofta (30–79 %) | I 1 tillstånd |
| INPP4Ainositol polyphosphate-4-phosphatase type I A | Ofta (30–79 %) | I 1 tillstånd |
| KYkyphoscoliosis peptidase | Ofta (30–79 %) | I 1 tillstånd |
| LYRM4LYR motif containing 4 | Ofta (30–79 %) | I 1 tillstånd |
| MECP2methyl-CpG binding protein 2 | Ofta (30–79 %) | I 1 tillstånd |
| MKS1MKS transition zone complex subunit 1 | Ofta (30–79 %) | I 1 tillstånd |
| MSL3MSL complex subunit 3 | Ofta (30–79 %) | I 1 tillstånd |
| MT-TEmitochondrially encoded tRNA-Glu (GAA/G) | Ofta (30–79 %) | I 1 tillstånd |
| MTRFRmitochondrial translation release factor in rescue | Ofta (30–79 %) | I 1 tillstånd |
| NR4A2nuclear receptor subfamily 4 group A member 2 | Ofta (30–79 %) | I 1 tillstånd |
| OCA2OCA2 melanosomal transmembrane protein | Ofta (30–79 %) | I 1 tillstånd |
| RAB3ARAB3A, member RAS oncogene family | Ofta (30–79 %) | I 1 tillstånd |
| REEP1receptor accessory protein 1 | Ofta (30–79 %) | I 1 tillstånd |
| RUBCNrubicon autophagy regulator | Ofta (30–79 %) | I 1 tillstånd |
| THtyrosine hydroxylase | Ofta (30–79 %) | I 1 tillstånd |
| TSPOAP1TSPO associated protein 1 | Ofta (30–79 %) | I 1 tillstånd |
| UBE3Aubiquitin protein ligase E3A | Ofta (30–79 %) | I 3 tillstånd |
| UCHL1ubiquitin C-terminal hydrolase L1 | Ofta (30–79 %) | I 1 tillstånd |
| USP8ubiquitin specific peptidase 8 | Ofta (30–79 %) | I 1 tillstånd |
| ZFYVE26zinc finger FYVE-type containing 26 | Ofta (30–79 %) | I 1 tillstånd |
| FTLferritin light chain | Ibland (5–29 %) | I 1 tillstånd |
| GJB1gap junction protein beta 1 | Ibland (5–29 %) | I 2 tillstånd |
| PLXNA1plexin A1 | Ibland (5–29 %) | I 1 tillstånd |
| RARS1arginyl-tRNA synthetase 1 | Ibland (5–29 %) | I 1 tillstånd |
| SYNE1spectrin repeat containing nuclear envelope protein 1 | Ibland (5–29 %) | I 1 tillstånd |
| TAF1TATA-box binding protein associated factor 1 | Ibland (5–29 %) | I 1 tillstånd |
| TRRAPtransformation/transcription domain associated protein | Ibland (5–29 %) | I 1 tillstånd |
| UFC1ubiquitin-fold modifier conjugating enzyme 1 | Ibland (5–29 %) | I 1 tillstånd |
| ZNF142zinc finger protein 142 | Ibland (5–29 %) | I 1 tillstånd |
| SPTAN1spectrin alpha, non-erythrocytic 1 | Sällan (1–4%) | I 1 tillstånd |
| APOEapolipoprotein E | Inte registrerat | I 1 tillstånd |
| DPM1dolichyl-phosphate mannosyltransferase subunit 1, catalytic | Inte registrerat | I 1 tillstånd |
| KDM5Clysine demethylase 5C | Inte registrerat | I 1 tillstånd |
| PDE8Bphosphodiesterase 8B | Inte registrerat | I 1 tillstånd |
| PSEN1presenilin 1 | Inte registrerat | I 1 tillstånd |
| SLC33A1solute carrier family 33 member 1 | Inte registrerat | I 1 tillstånd |
| ST3GAL5ST3 beta-galactoside alpha-2,3-sialyltransferase 5 | Inte registrerat | I 1 tillstånd |
| SUMF1sulfatase modifying factor 1 | Inte registrerat | I 1 tillstånd |
| TREX1three prime repair exonuclease 1 | Inte registrerat | I 1 tillstånd |
Hur ofta det förekommer hos personer med ett av genens tillstånd, den vanligaste frekvensen bland dem, enligt Human Phenotype Ontology. Dessa sidor beskriver egenskaper och forskningen bakom dem. De är inte en diagnos, och det är läkare eller genetisk rådgivare du bör fråga om symtom.
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Varifrån informationen kommer
- Human Phenotype Ontology, version 2026-09-01: egenskapen, dess namn, definition och de gener som är kopplade till den. Läs mer på hpo.jax.org.
- Dataversion 2026.10.18-8b139e39.
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From traits to your genome
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.
Från 449 $
Fri frakt · Resultat inom 6–8 veckor
