Merkmal
Nerve damage causing decreased feeling and movement
Klinische Bezeichnung: Sensorimotor neuropathy
Zusammenfassung
- Auch genannt
- Mixed polyneuropathy, Sensorimotor peripheral neuropathy
- Körpersystem
- Abnormality of the nervous system
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page$trait$nameLesen Sie die Gene aus, die mit Nerve damage causing decreased feeling and movement 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.
- Rare Hereditary Peripheral NeuropathiesReads 50 of these genesCLCF1LITAFPOLGRAB7ASPTLC2TYMPAbout this report →
- Charcot-Marie-Tooth DiseaseReads 21 of these genesLITAFRAB7AAIFM1GDAP1MMENEFLAbout this report →
- Inherited Neurodegenerative DisordersReads 39 of these genesAFG3L2POLGXRCC1GALCPSAPSETXAbout this report →
- Hereditary Optic NeuropathyReads 7 of these genesAFG3L2DNM1LMT-ND1MT-ND4MT-ND5MT-ND6About this report →
Show 52 more reports
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 10 of these genesXRCC1SETXPEX6RFC1SACSTDP1About this report →
- Leigh SyndromeReads 11 of these genesAIFM1MT-ATP6MT-ND1MT-ND3MT-ND4MT-ND5About this report →
- Peroxisomal Enzyme Disorders & Refsum DiseaseReads 3 of these genesHSD17B4AMACRPHYHAbout this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 5 of these genesCLCF1SPTLC2AIFM1KIF1ARFC1About this report →
- Deficiency of Adenosine Deaminase 2 (DADA2)Reads 1 of these genesADA2About this report →
- Gaucher DiseaseReads 1 of these genesGBA1About this report →
- Hereditary Neuropathy with Liability to Pressure Palsies (HNPP)Reads 1 of these genesPMP22About this report →
- KIF5A-Related Amyotrophic Lateral SclerosisReads 1 of these genesKIF5AAbout this report →
- Krabbe DiseaseReads 1 of these genesGALCAbout this report →
- MCM3AP-Related Peripheral NeuropathyReads 1 of these genesMCM3APAbout this report →
- NGLY1 DeficiencyReads 1 of these genesNGLY1About this report →
- OPA1-Related Optic AtrophyReads 1 of these genesOPA1About this report →
- X-Linked Adrenoleukodystrophy (ABCD1)Reads 1 of these genesABCD1About this report →
- Hereditary Spastic ParaplegiaReads 8 of these genesSPG11TFGABCD1B4GALNT1GBA2KIF1AAbout this report →
- Primary Mitochondrial DiseaseReads 11 of these genesAFG3L2POLGTYMPAIFM1LIG3RRM2BAbout this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 4 of these genesSPTLC2SETXSPG11VCPAbout this report →
- Encephalopathy due to Mitochondrial and Peroxisomal Fission DefectReads 1 of these genesDNM1LAbout this report →
- Hereditary Manganese Transporter DisordersReads 1 of these genesSLC30A10About this report →
- Metachromatic LeukodystrophyReads 1 of these genesPSAPAbout this report →
- Riboflavin Transporter DeficiencyReads 1 of these genesSLC52A2About this report →
- Other Inherited LeukodystrophiesReads 6 of these genesGALCPSAPABCD1PEX6PEX7RPIAAbout this report →
- Pontocerebellar Hypoplasia (TSEN54 and MINPP1)Reads 3 of these genesCLP1SLC25A46VRK1About this report →
- Spinal Muscular AtrophyReads 3 of these genesEMILIN1VRK1IGHMBP2About this report →
- Zellweger Spectrum & Peroxisome Biogenesis DisordersReads 2 of these genesPEX6PEX7About this report →
- Parkinson DiseaseReads 2 of these genesPLA2G6GBA1About this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 3 of these genesAFG3L2PPP2R2BPDYNAbout this report →
- Fatty Acid Oxidation & Carnitine Cycle DisordersReads 2 of these genesHADHAHADHBAbout this report →
- DNA Repair DiseaseReads 3 of these genesSETXTDP1MRE11About this report →
- Lysosomal Storage DiseaseReads 3 of these genesGALCPSAPGBA1About this report →
- Hepatic Porphyria DisordersReads 1 of these genesHMBSAbout this report →
- PorphyriaReads 1 of these genesHMBSAbout this report →
- Neurodegeneration with Brain Iron Accumulation (NBIA)Reads 1 of these genesPLA2G6About this report →
- Familial HypomagnesemiaReads 1 of these genesATP1A1About this report →
- Hereditary AmyloidosisReads 1 of these genesB2MAbout this report →
- Frontotemporal DementiaReads 1 of these genesVCPAbout this report →
- Hypertrophic CardiomyopathyReads 2 of these genesDHHHADHAAbout this report →
- Cutis LaxaReads 1 of these genesEMILIN1About this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 1 of these genesDHHAbout this report →
- Distal MyopathiesReads 1 of these genesVCPAbout this report →
- GPI Anchor Biosynthesis DefectsReads 1 of these genesPIGBAbout this report →
- Homocystinuria & Cobalamin DisordersReads 1 of these genesAHCYAbout this report →
- Epilepsy (Full Panel)Reads 3 of these genesPNKPSCARB2PIGBAbout this report →
- Congenital Muscular DystrophiesReads 1 of these genesLAMA2About this report →
- Diabetes MellitusReads 1 of these genesMT-TL1About this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesLAMA2About this report →
- Osteogenesis ImperfectaReads 1 of these genesPPIBAbout this report →
- Rare Monogenic Autoinflammatory DiseasesReads 1 of these genesADA2About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesPNKPAbout this report →
- Female InfertilityReads 1 of these genesHSD17B4About this report →
- Intellectual DisabilityReads 2 of these genesKIF1AVRK1About this report →
- Hearing Loss and DeafnessReads 1 of these genesAIFM1About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesB2MAbout this report →
Lesen Sie die Gene aus, die mit Nerve damage causing decreased feeling and movement zusammenhängen, und den Rest Ihres Genoms, mit einem einzigen Test.
Ab 449 $Kostenloser Versand · Ergebnisse in 6–8 Wochen
Meinen Genome Test bestellen107 Gene mit Nerve damage causing decreased feeling and movement verknüpft
Veränderungen in diesen Genen verursachen seltene Erkrankungen, bei denen Nerve damage causing decreased feeling and movement 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 |
|---|---|---|
| AFG3L2AFG3 like matrix AAA peptidase subunit 2 | Immer | In 2 Erkrankungen |
| ARHGAP19Rho GTPase activating protein 19 | Immer | In 1 Erkrankung |
| CLCF1cardiotrophin like cytokine factor 1 | Immer | In 1 Erkrankung |
| COA3cytochrome c oxidase assembly factor 3 | Immer | In 1 Erkrankung |
| GET4guided entry of tail-anchored proteins factor 4 | Immer | In 1 Erkrankung |
| HMBShydroxymethylbilane synthase | Immer | In 2 Erkrankungen |
| HSD17B4hydroxysteroid 17-beta dehydrogenase 4 | Immer | In 1 Erkrankung |
| LAMA2laminin subunit alpha 2 | Immer | In 2 Erkrankungen |
| LITAFlipopolysaccharide induced TNF factor | Immer | In 1 Erkrankung |
| MCM3APminichromosome maintenance complex component 3 associated protein | Immer | In 1 Erkrankung |
| POLGDNA polymerase gamma, catalytic subunit | Immer | In 2 Erkrankungen |
| RAB7ARAB7A, member RAS oncogene family | Immer | In 1 Erkrankung |
| RCC1regulator of chromosome condensation 1 | Immer | In 1 Erkrankung |
| SPTLC2serine palmitoyltransferase long chain base subunit 2 | Immer | In 1 Erkrankung |
| TYMPthymidine phosphorylase | Immer | In 2 Erkrankungen |
| XRCC1X-ray repair cross complementing 1 | Immer | In 1 Erkrankung |
| ADA2adenosine deaminase 2 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| AIFM1apoptosis inducing factor mitochondria associated 1 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| DHHdesert hedgehog signaling molecule | Sehr häufig (80–99 %) | In 1 Erkrankung |
| GALCgalactosylceramidase | Sehr häufig (80–99 %) | In 4 Erkrankungen |
| GDAP1ganglioside induced differentiation associated protein 1 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| LIG3DNA ligase 3 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| MMEmembrane metalloendopeptidase | Sehr häufig (80–99 %) | In 3 Erkrankungen |
| NEFLneurofilament light chain | Sehr häufig (80–99 %) | In 3 Erkrankungen |
| NGLY1N-glycanase 1 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| PDK3pyruvate dehydrogenase kinase 3 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| PIK3R5phosphoinositide-3-kinase regulatory subunit 5 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| PSAPprosaposin | Sehr häufig (80–99 %) | In 1 Erkrankung |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| SETXsenataxin | Sehr häufig (80–99 %) | In 1 Erkrankung |
| SH3TC2SH3 domain and tetratricopeptide repeats 2 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| SPG11SPG11 vesicle trafficking associated, spatacsin | Sehr häufig (80–99 %) | In 1 Erkrankung |
| TFGtrafficking from ER to golgi regulator | Sehr häufig (80–99 %) | In 1 Erkrankung |
| ABCD1ATP binding cassette subfamily D member 1 | Häufig (30–79 %) | In 1 Erkrankung |
| AMACRalpha-methylacyl-CoA racemase | Häufig (30–79 %) | In 2 Erkrankungen |
| B4GALNT1beta-1,4-N-acetyl-galactosaminyltransferase 1 | Häufig (30–79 %) | In 1 Erkrankung |
| CLP1cleavage factor polyribonucleotide kinase subunit 1 | Häufig (30–79 %) | In 1 Erkrankung |
| COA8cytochrome c oxidase assembly factor 8 | Häufig (30–79 %) | In 1 Erkrankung |
| DNAJC3DnaJ heat shock protein family (Hsp40) member C3 | Häufig (30–79 %) | In 1 Erkrankung |
| DNM1Ldynamin 1L | Häufig (30–79 %) | In 1 Erkrankung |
67 weitere Gene anzeigen
| Gen | Wie häufig es auftritt | Erkrankungen |
|---|---|---|
| EMILIN1elastin microfibril interfacer 1 | Häufig (30–79 %) | In 1 Erkrankung |
| GBA2glucosylceramidase beta 2 | Häufig (30–79 %) | In 1 Erkrankung |
| GJB1gap junction protein beta 1 | Häufig (30–79 %) | In 1 Erkrankung |
| IFRD1interferon related developmental regulator 1 | Häufig (30–79 %) | In 1 Erkrankung |
| KIF1Akinesin family member 1A | Häufig (30–79 %) | In 2 Erkrankungen |
| MPZmyelin protein zero | Häufig (30–79 %) | In 1 Erkrankung |
| MT-ATP6mitochondrially encoded ATP synthase membrane subunit 6 | Häufig (30–79 %) | In 1 Erkrankung |
| MT-ND1mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 | Häufig (30–79 %) | In 2 Erkrankungen |
| MT-ND2mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 | Häufig (30–79 %) | In 1 Erkrankung |
| MT-ND3mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 | Häufig (30–79 %) | In 1 Erkrankung |
| MT-ND4mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 | Häufig (30–79 %) | In 2 Erkrankungen |
| MT-ND5mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 | Häufig (30–79 %) | In 2 Erkrankungen |
| MT-ND6mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 | Häufig (30–79 %) | In 2 Erkrankungen |
| MT-TKmitochondrially encoded tRNA-Lys (AAA/G) | Häufig (30–79 %) | In 1 Erkrankung |
| MT-TL1mitochondrially encoded tRNA-Leu (UUA/G) 1 | Häufig (30–79 %) | In 2 Erkrankungen |
| MT-TVmitochondrially encoded tRNA-Val (GUN) | Häufig (30–79 %) | In 1 Erkrankung |
| MT-TWmitochondrially encoded tRNA-Trp (UGA/G) | Häufig (30–79 %) | In 2 Erkrankungen |
| OPA1OPA1 mitochondrial dynamin like GTPase | Häufig (30–79 %) | In 2 Erkrankungen |
| PEX6peroxisomal biogenesis factor 6 | Häufig (30–79 %) | In 1 Erkrankung |
| PLA2G6phospholipase A2 group VI | Häufig (30–79 %) | In 1 Erkrankung |
| PMP22peripheral myelin protein 22 | Häufig (30–79 %) | In 2 Erkrankungen |
| PPIBpeptidylprolyl isomerase B | Häufig (30–79 %) | In 1 Erkrankung |
| RFC1replication factor C subunit 1 | Häufig (30–79 %) | In 1 Erkrankung |
| SACSsacsin molecular chaperone | Häufig (30–79 %) | In 1 Erkrankung |
| SCO2synthesis of cytochrome C oxidase 2 | Häufig (30–79 %) | In 1 Erkrankung |
| SLC25A46solute carrier family 25 member 46 | Häufig (30–79 %) | In 1 Erkrankung |
| TDP1tyrosyl-DNA phosphodiesterase 1 | Häufig (30–79 %) | In 1 Erkrankung |
| UCHL1ubiquitin C-terminal hydrolase L1 | Häufig (30–79 %) | In 1 Erkrankung |
| VCPvalosin containing protein | Häufig (30–79 %) | In 1 Erkrankung |
| VPS13Dvacuolar protein sorting 13 homolog D | Häufig (30–79 %) | In 1 Erkrankung |
| VPS41VPS41 subunit of HOPS complex | Häufig (30–79 %) | In 1 Erkrankung |
| VRK1VRK serine/threonine kinase 1 | Häufig (30–79 %) | In 1 Erkrankung |
| AHCYadenosylhomocysteinase | Manchmal (5–29 %) | In 1 Erkrankung |
| B2Mbeta-2-microglobulin | Manchmal (5–29 %) | In 1 Erkrankung |
| GBA1glucosylceramidase beta 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| KIF5Akinesin family member 5A | Manchmal (5–29 %) | In 1 Erkrankung |
| MRE11MRE11 double strand break repair nuclease | Manchmal (5–29 %) | In 1 Erkrankung |
| MT-CO1mitochondrially encoded cytochrome c oxidase I | Manchmal (5–29 %) | In 1 Erkrankung |
| MT-CO2mitochondrially encoded cytochrome c oxidase II | Manchmal (5–29 %) | In 1 Erkrankung |
| MT-CO3mitochondrially encoded cytochrome c oxidase III | Manchmal (5–29 %) | In 1 Erkrankung |
| MT-TFmitochondrially encoded tRNA-Phe (UUU/C) | Manchmal (5–29 %) | In 1 Erkrankung |
| MT-THmitochondrially encoded tRNA-His (CAU/C) | Manchmal (5–29 %) | In 1 Erkrankung |
| MT-TQmitochondrially encoded tRNA-Gln (CAA/G) | Manchmal (5–29 %) | In 1 Erkrankung |
| MT-TS1mitochondrially encoded tRNA-Ser (UCN) 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| MT-TS2mitochondrially encoded tRNA-Ser (AGU/C) 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| PNKPpolynucleotide kinase 3'-phosphatase | Manchmal (5–29 %) | In 1 Erkrankung |
| PPP2R2Bprotein phosphatase 2 regulatory subunit Bbeta | Manchmal (5–29 %) | In 2 Erkrankungen |
| RNASEH1ribonuclease H1 | Manchmal (5–29 %) | In 1 Erkrankung |
| RRM1ribonucleotide reductase catalytic subunit M1 | Manchmal (5–29 %) | In 1 Erkrankung |
| SCARB2scavenger receptor class B member 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| SLC30A10solute carrier family 30 member 10 | Manchmal (5–29 %) | In 1 Erkrankung |
| HADHAhydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha | Selten (1–4 %) | In 1 Erkrankung |
| HADHBhydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta | Selten (1–4 %) | In 1 Erkrankung |
| ABHD12abhydrolase domain containing 12, lysophospholipase | Nicht erfasst | In 1 Erkrankung |
| ATP1A1ATPase Na+/K+ transporting subunit alpha 1 | Nicht erfasst | In 1 Erkrankung |
| FDX2ferredoxin 2 | Nicht erfasst | In 1 Erkrankung |
| IARS2isoleucyl-tRNA synthetase 2, mitochondrial | Nicht erfasst | In 1 Erkrankung |
| IGHMBP2immunoglobulin mu DNA binding protein 2 | Nicht erfasst | In 1 Erkrankung |
| MPV17mitochondrial inner membrane protein MPV17 | Nicht erfasst | In 1 Erkrankung |
| NEFHneurofilament heavy chain | Nicht erfasst | In 1 Erkrankung |
| PDYNprodynorphin | Nicht erfasst | In 1 Erkrankung |
| PEX7peroxisomal biogenesis factor 7 | Nicht erfasst | In 1 Erkrankung |
| PHYHphytanoyl-CoA 2-hydroxylase | Nicht erfasst | In 1 Erkrankung |
| PIGBphosphatidylinositol glycan anchor biosynthesis class B | Nicht erfasst | In 1 Erkrankung |
| RPIAribose 5-phosphate isomerase A | Nicht erfasst | In 1 Erkrankung |
| SCYL1SCY1 like pseudokinase 1 | Nicht erfasst | In 1 Erkrankung |
| SLC52A2solute carrier family 52 member 2 | 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.
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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