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Egenskap
Peripheral neuropathy
Peripheral neuropathy is a general term for any disorder of the peripheral nervous system. The main clinical features used to classify peripheral neuropathy are distribution, type (mainly demyelinating versus mainly axonal), duration, and course.
Sammendrag
- Også kalt
- Peripheral nerve damage, Peripheral neuritis
- Kroppssystem
- Abnormality of the nervous system
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Denne siden som data
Legg til .json etter adressen til siden, eller be om application/json, for å lese den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/peripheral-neuropathy.json"
page <- fromJSON(url)
page$trait$namePeripheral neuropathyHP:0009830
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Les genene knyttet til Peripheral neuropathy, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test271 gener knyttet til Peripheral neuropathy
Endringer i disse genene forårsaker sjeldne tilstander der Peripheral neuropathy forekommer. De fleste med denne egenskapen har ingen av disse tilstandene, og et gen på denne listen sier ingenting om noens eget genom.
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| ACER3alkaline ceramidase 3 | Alltid | I 1 tilstand |
| AFG3L2AFG3 like matrix AAA peptidase subunit 2 | Alltid | I 1 tilstand |
| BAG3BAG cochaperone 3 | Alltid | I 1 tilstand |
| C19orf12chromosome 19 open reading frame 12 | Alltid | I 1 tilstand |
| CADM3cell adhesion molecule 3 | Alltid | I 1 tilstand |
| DARS2aspartyl-tRNA synthetase 2, mitochondrial | Alltid | I 1 tilstand |
| DMXL2Dmx like 2 | Alltid | I 1 tilstand |
| DNAJC3DnaJ heat shock protein family (Hsp40) member C3 | Alltid | I 1 tilstand |
| EEFSECeukaryotic elongation factor, selenocysteine-tRNA specific | Alltid | I 1 tilstand |
| EGR2early growth response 2 | Alltid | I 2 tilstander |
| GDAP1ganglioside induced differentiation associated protein 1 | Alltid | I 1 tilstand |
| GTPBP2GTP binding protein 2 | Alltid | I 1 tilstand |
| HSPB8heat shock protein family B (small) member 8 | Alltid | I 1 tilstand |
| IARS2isoleucyl-tRNA synthetase 2, mitochondrial | Alltid | I 3 tilstander |
| INF2inverted formin 2 | Alltid | I 1 tilstand |
| ITPR3inositol 1,4,5-trisphosphate receptor type 3 | Alltid | I 1 tilstand |
| MFN2mitofusin 2 | Alltid | I 2 tilstander |
| NDC1NDC1 transmembrane nucleoporin | Alltid | I 1 tilstand |
| NGFnerve growth factor | Alltid | I 1 tilstand |
| OPA1OPA1 mitochondrial dynamin like GTPase | Alltid | I 3 tilstander |
| PDSS1decaprenyl diphosphate synthase subunit 1 | Alltid | I 1 tilstand |
| PEX5peroxisomal biogenesis factor 5 | Alltid | I 1 tilstand |
| PNKPpolynucleotide kinase 3'-phosphatase | Alltid | I 2 tilstander |
| POLGDNA polymerase gamma, catalytic subunit | Alltid | I 5 tilstander |
| PRPS1phosphoribosyl pyrophosphate synthetase 1 | Alltid | I 6 tilstander |
| PSAPprosaposin | Alltid | I 2 tilstander |
| REEP1receptor accessory protein 1 | Alltid | I 1 tilstand |
| RFC1replication factor C subunit 1 | Alltid | I 1 tilstand |
| RFC4replication factor C subunit 4 | Alltid | I 1 tilstand |
| SCO2synthesis of cytochrome C oxidase 2 | Alltid | I 1 tilstand |
| SCP2sterol carrier protein 2 | Alltid | I 1 tilstand |
| SPTAN1spectrin alpha, non-erythrocytic 1 | Alltid | I 1 tilstand |
| TYMPthymidine phosphorylase | Alltid | I 2 tilstander |
| ABCD1ATP binding cassette subfamily D member 1 | Svært ofte (80–99 %) | I 2 tilstander |
| AIFM1apoptosis inducing factor mitochondria associated 1 | Svært ofte (80–99 %) | I 1 tilstand |
| AP1B1adaptor related protein complex 1 subunit beta 1 | Svært ofte (80–99 %) | I 1 tilstand |
| AP1S1adaptor related protein complex 1 subunit sigma 1 | Svært ofte (80–99 %) | I 2 tilstander |
| APTXaprataxin | Svært ofte (80–99 %) | I 1 tilstand |
| ATXN1ataxin 1 | Svært ofte (80–99 %) | I 2 tilstander |
| ATXN3ataxin 3 | Svært ofte (80–99 %) | I 2 tilstander |
Vis 231 gener til
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| CCT5chaperonin containing TCP1 subunit 5 | Svært ofte (80–99 %) | I 1 tilstand |
| ELP1elongator acetyltransferase complex subunit 1 | Svært ofte (80–99 %) | I 1 tilstand |
| GBE11,4-alpha-glucan branching enzyme 1 | Svært ofte (80–99 %) | I 1 tilstand |
| GCLCglutamate-cysteine ligase catalytic subunit | Svært ofte (80–99 %) | I 1 tilstand |
| LYSTlysosomal trafficking regulator | Svært ofte (80–99 %) | I 2 tilstander |
| MYOTmyotilin | Svært ofte (80–99 %) | I 1 tilstand |
| PEX7peroxisomal biogenesis factor 7 | Svært ofte (80–99 %) | I 1 tilstand |
| PHYHphytanoyl-CoA 2-hydroxylase | Svært ofte (80–99 %) | I 1 tilstand |
| PMP22peripheral myelin protein 22 | Svært ofte (80–99 %) | I 3 tilstander |
| SCN10Asodium voltage-gated channel alpha subunit 10 | Svært ofte (80–99 %) | I 1 tilstand |
| SCN11Asodium voltage-gated channel alpha subunit 11 | Svært ofte (80–99 %) | I 1 tilstand |
| SCN9Asodium voltage-gated channel alpha subunit 9 | Svært ofte (80–99 %) | I 2 tilstander |
| SOX10SRY-box transcription factor 10 | Svært ofte (80–99 %) | I 1 tilstand |
| TFGtrafficking from ER to golgi regulator | Svært ofte (80–99 %) | I 2 tilstander |
| TTPAalpha tocopherol transfer protein | Svært ofte (80–99 %) | I 1 tilstand |
| ALADaminolevulinate dehydratase | Ofte (30–79 %) | I 1 tilstand |
| ATP5F1AATP synthase F1 subunit alpha | Ofte (30–79 %) | I 1 tilstand |
| ATP5F1DATP synthase F1 subunit delta | Ofte (30–79 %) | I 1 tilstand |
| ATP5F1EATP synthase F1 subunit epsilon | Ofte (30–79 %) | I 2 tilstander |
| ATP5MKATP synthase membrane subunit k | Ofte (30–79 %) | I 1 tilstand |
| ATP5POATP synthase peripheral stalk subunit OSCP | Ofte (30–79 %) | I 1 tilstand |
| ATPAF2ATP synthase mitochondrial F1 complex assembly factor 2 | Ofte (30–79 %) | I 1 tilstand |
| BORCS5BLOC-1 related complex subunit 5 | Ofte (30–79 %) | I 1 tilstand |
| CAPN1calpain 1 | Ofte (30–79 %) | I 2 tilstander |
| CTLA4cytotoxic T-lymphocyte associated protein 4 | Ofte (30–79 %) | I 2 tilstander |
| CYP27A1cytochrome P450 family 27 subfamily A member 1 | Ofte (30–79 %) | I 2 tilstander |
| DCAF17DDB1 and CUL4 associated factor 17 | Ofte (30–79 %) | I 1 tilstand |
| ELOVL5ELOVL fatty acid elongase 5 | Ofte (30–79 %) | I 1 tilstand |
| EMILIN1elastin microfibril interfacer 1 | Ofte (30–79 %) | I 1 tilstand |
| ERBB3erb-b2 receptor tyrosine kinase 3 | Ofte (30–79 %) | I 1 tilstand |
| ERCC6ERCC excision repair 6, chromatin remodeling factor | Ofte (30–79 %) | I 3 tilstander |
| ERCC8ERCC excision repair 8, CSA ubiquitin ligase complex subunit | Ofte (30–79 %) | I 1 tilstand |
| FMR1fragile X messenger ribonucleoprotein 1 | Ofte (30–79 %) | I 2 tilstander |
| GALCgalactosylceramidase | Ofte (30–79 %) | I 3 tilstander |
| HADHAhydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha | Ofte (30–79 %) | I 3 tilstander |
| HADHBhydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta | Ofte (30–79 %) | I 2 tilstander |
| HLA-DPA1major histocompatibility complex, class II, DP alpha 1 | Ofte (30–79 %) | I 1 tilstand |
| HLA-DPB1major histocompatibility complex, class II, DP beta 1 | Ofte (30–79 %) | I 1 tilstand |
| HMBShydroxymethylbilane synthase | Ofte (30–79 %) | I 1 tilstand |
| LETM1leucine zipper and EF-hand containing transmembrane protein 1 | Ofte (30–79 %) | I 1 tilstand |
| LIG3DNA ligase 3 | Ofte (30–79 %) | I 1 tilstand |
| LRPPRCleucine rich pentatricopeptide repeat containing | Ofte (30–79 %) | I 1 tilstand |
| MARS1methionyl-tRNA synthetase 1 | Ofte (30–79 %) | I 1 tilstand |
| MT-ATP6mitochondrially encoded ATP synthase membrane subunit 6 | Ofte (30–79 %) | I 2 tilstander |
| MT-ATP8mitochondrially encoded ATP synthase membrane subunit 8 | Ofte (30–79 %) | I 1 tilstand |
| MT-CO1mitochondrially encoded cytochrome c oxidase I | Ofte (30–79 %) | I 2 tilstander |
| MT-CO2mitochondrially encoded cytochrome c oxidase II | Ofte (30–79 %) | I 1 tilstand |
| MT-CO3mitochondrially encoded cytochrome c oxidase III | Ofte (30–79 %) | I 2 tilstander |
| MT-ND1mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 | Ofte (30–79 %) | I 2 tilstander |
| MT-ND4mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 | Ofte (30–79 %) | I 2 tilstander |
| MT-ND5mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 | Ofte (30–79 %) | I 2 tilstander |
| MT-ND6mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 | Ofte (30–79 %) | I 2 tilstander |
| MT-TFmitochondrially encoded tRNA-Phe (UUU/C) | Ofte (30–79 %) | I 1 tilstand |
| MT-THmitochondrially encoded tRNA-His (CAU/C) | Ofte (30–79 %) | I 1 tilstand |
| MT-TL1mitochondrially encoded tRNA-Leu (UUA/G) 1 | Ofte (30–79 %) | I 1 tilstand |
| MT-TQmitochondrially encoded tRNA-Gln (CAA/G) | Ofte (30–79 %) | I 1 tilstand |
| MT-TS1mitochondrially encoded tRNA-Ser (UCN) 1 | Ofte (30–79 %) | I 1 tilstand |
| MT-TS2mitochondrially encoded tRNA-Ser (AGU/C) 2 | Ofte (30–79 %) | I 1 tilstand |
| MT-TWmitochondrially encoded tRNA-Trp (UGA/G) | Ofte (30–79 %) | I 1 tilstand |
| MTHFRmethylenetetrahydrofolate reductase | Ofte (30–79 %) | I 1 tilstand |
| MTRFRmitochondrial translation release factor in rescue | Ofte (30–79 %) | I 1 tilstand |
| MYH14myosin heavy chain 14 | Ofte (30–79 %) | I 2 tilstander |
| NAGAalpha-N-acetylgalactosaminidase | Ofte (30–79 %) | I 2 tilstander |
| NARS1asparaginyl-tRNA synthetase 1 | Ofte (30–79 %) | I 2 tilstander |
| NGLY1N-glycanase 1 | Ofte (30–79 %) | I 1 tilstand |
| PDE4Dphosphodiesterase 4D | Ofte (30–79 %) | I 1 tilstand |
| PLA2G6phospholipase A2 group VI | Ofte (30–79 %) | I 1 tilstand |
| PNPLA6patatin like domain 6, lysophospholipase | Ofte (30–79 %) | I 2 tilstander |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Ofte (30–79 %) | I 1 tilstand |
| PRTN3proteinase 3 | Ofte (30–79 %) | I 1 tilstand |
| PTPN22protein tyrosine phosphatase non-receptor type 22 | Ofte (30–79 %) | I 2 tilstander |
| RAI1retinoic acid induced 1 | Ofte (30–79 %) | I 2 tilstander |
| RRM1ribonucleotide reductase catalytic subunit M1 | Ofte (30–79 %) | I 1 tilstand |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Ofte (30–79 %) | I 2 tilstander |
| SACSsacsin molecular chaperone | Ofte (30–79 %) | I 1 tilstand |
| SCYL1SCY1 like pseudokinase 1 | Ofte (30–79 %) | I 1 tilstand |
| SLC12A6solute carrier family 12 member 6 | Ofte (30–79 %) | I 1 tilstand |
| SLC30A10solute carrier family 30 member 10 | Ofte (30–79 %) | I 1 tilstand |
| SLC46A1solute carrier family 46 member 1 | Ofte (30–79 %) | I 2 tilstander |
| SNAP29synaptosome associated protein 29 | Ofte (30–79 %) | I 2 tilstander |
| TDP1tyrosyl-DNA phosphodiesterase 1 | Ofte (30–79 %) | I 1 tilstand |
| TIMMDC1translocase of inner mitochondrial membrane domain containing 1 | Ofte (30–79 %) | I 1 tilstand |
| TK2thymidine kinase 2 | Ofte (30–79 %) | I 1 tilstand |
| TNXBtenascin XB | Ofte (30–79 %) | I 1 tilstand |
| TOP3ADNA topoisomerase III alpha | Ofte (30–79 %) | I 1 tilstand |
| TRMT5tRNA methyltransferase 5 | Ofte (30–79 %) | I 1 tilstand |
| ZFRzinc finger RNA binding protein | Ofte (30–79 %) | I 1 tilstand |
| AARS1alanyl-tRNA synthetase 1 | Noen ganger (5–29 %) | I 2 tilstander |
| ABCC8ATP binding cassette subfamily C member 8 | Noen ganger (5–29 %) | I 1 tilstand |
| ADA2adenosine deaminase 2 | Noen ganger (5–29 %) | I 2 tilstander |
| ALDH4A1aldehyde dehydrogenase 4 family member A1 | Noen ganger (5–29 %) | I 1 tilstand |
| AP5Z1adaptor related protein complex 5 subunit zeta 1 | Noen ganger (5–29 %) | I 2 tilstander |
| ATL1atlastin GTPase 1 | Noen ganger (5–29 %) | I 2 tilstander |
| ATP6V1B2ATPase H+ transporting V1 subunit B2 | Noen ganger (5–29 %) | I 1 tilstand |
| BMP6bone morphogenetic protein 6 | Noen ganger (5–29 %) | I 1 tilstand |
| BRD4bromodomain containing 4 | Noen ganger (5–29 %) | I 1 tilstand |
| BTNL2butyrophilin like 2 | Noen ganger (5–29 %) | I 1 tilstand |
| CARS1cysteinyl-tRNA synthetase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| CBLIFcobalamin binding intrinsic factor | Noen ganger (5–29 %) | I 1 tilstand |
| CCND1cyclin D1 | Noen ganger (5–29 %) | I 1 tilstand |
| CD28CD28 molecule | Noen ganger (5–29 %) | I 1 tilstand |
| CD4CD4 molecule | Noen ganger (5–29 %) | I 1 tilstand |
| CISD2CDGSH iron sulfur domain 2 | Noen ganger (5–29 %) | I 1 tilstand |
| DBR1debranching RNA lariats 1 | Noen ganger (5–29 %) | I 1 tilstand |
| DDB2damage specific DNA binding protein 2 | Noen ganger (5–29 %) | I 1 tilstand |
| DNAJC30DnaJ heat shock protein family (Hsp40) member C30 | Noen ganger (5–29 %) | I 1 tilstand |
| DNASE1L3deoxyribonuclease 1L3 | Noen ganger (5–29 %) | I 1 tilstand |
| DNMT1DNA methyltransferase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| DPM1dolichyl-phosphate mannosyltransferase subunit 1, catalytic | Noen ganger (5–29 %) | I 1 tilstand |
| DSTYKdual serine/threonine and tyrosine protein kinase | Noen ganger (5–29 %) | I 1 tilstand |
| ERCC1ERCC excision repair 1, endonuclease non-catalytic subunit | Noen ganger (5–29 %) | I 1 tilstand |
| ERCC2ERCC excision repair 2, TFIIH core complex helicase subunit | Noen ganger (5–29 %) | I 3 tilstander |
| ERCC3ERCC excision repair 3, TFIIH core complex helicase subunit | Noen ganger (5–29 %) | I 2 tilstander |
| ERCC4ERCC excision repair 4, endonuclease catalytic subunit | Noen ganger (5–29 %) | I 1 tilstand |
| ERCC5ERCC excision repair 5, endonuclease | Noen ganger (5–29 %) | I 2 tilstander |
| FBN1fibrillin 1 | Noen ganger (5–29 %) | I 2 tilstander |
| FLNCfilamin C | Noen ganger (5–29 %) | I 1 tilstand |
| GTF2E2general transcription factor IIE subunit 2 | Noen ganger (5–29 %) | I 1 tilstand |
| GTF2H5general transcription factor IIH subunit 5 | Noen ganger (5–29 %) | I 1 tilstand |
| GUK1guanylate kinase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| HADHhydroxyacyl-CoA dehydrogenase | Noen ganger (5–29 %) | I 1 tilstand |
| HDAC8histone deacetylase 8 | Noen ganger (5–29 %) | I 1 tilstand |
| HFEhomeostatic iron regulator | Noen ganger (5–29 %) | I 1 tilstand |
| HLA-Bmajor histocompatibility complex, class I, B | Noen ganger (5–29 %) | I 1 tilstand |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Noen ganger (5–29 %) | I 2 tilstander |
| HSD3B7hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7 | Noen ganger (5–29 %) | I 1 tilstand |
| INSRinsulin receptor | Noen ganger (5–29 %) | I 1 tilstand |
| IRF4interferon regulatory factor 4 | Noen ganger (5–29 %) | I 1 tilstand |
| KCNJ11potassium inwardly rectifying channel subfamily J member 11 | Noen ganger (5–29 %) | I 1 tilstand |
| MAU2MAU2 sister chromatid cohesion factor | Noen ganger (5–29 %) | I 1 tilstand |
| MPC1mitochondrial pyruvate carrier 1 | Noen ganger (5–29 %) | I 1 tilstand |
| MPLKIPM-phase specific PLK1 interacting protein | Noen ganger (5–29 %) | I 1 tilstand |
| MPV17mitochondrial inner membrane protein MPV17 | Noen ganger (5–29 %) | I 1 tilstand |
| MT-CYBmitochondrially encoded cytochrome b | Noen ganger (5–29 %) | I 1 tilstand |
| MT-ND2mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 | Noen ganger (5–29 %) | I 1 tilstand |
| MT-ND4Lmitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L | Noen ganger (5–29 %) | I 1 tilstand |
| MT-TKmitochondrially encoded tRNA-Lys (AAA/G) | Noen ganger (5–29 %) | I 1 tilstand |
| MTRR5-methyltetrahydrofolate-homocysteine methyltransferase reductase | Noen ganger (5–29 %) | I 1 tilstand |
| MYD88MYD88 innate immune signal transduction adaptor | Noen ganger (5–29 %) | I 1 tilstand |
| NARS2asparaginyl-tRNA synthetase 2, mitochondrial | Noen ganger (5–29 %) | I 1 tilstand |
| NDUFS2NADH:ubiquinone oxidoreductase core subunit S2 | Noen ganger (5–29 %) | I 1 tilstand |
| NEFLneurofilament light chain | Noen ganger (5–29 %) | I 1 tilstand |
| NFU1NFU1 iron-sulfur cluster scaffold | Noen ganger (5–29 %) | I 1 tilstand |
| NIPBLNIPBL cohesin loading factor | Noen ganger (5–29 %) | I 1 tilstand |
| NOTCH2notch receptor 2 | Noen ganger (5–29 %) | I 1 tilstand |
| NOTCH3notch receptor 3 | Noen ganger (5–29 %) | I 1 tilstand |
| P4HA2prolyl 4-hydroxylase subunit alpha 2 | Noen ganger (5–29 %) | I 1 tilstand |
| PEX1peroxisomal biogenesis factor 1 | Noen ganger (5–29 %) | I 1 tilstand |
| PEX16peroxisomal biogenesis factor 16 | Noen ganger (5–29 %) | I 1 tilstand |
| PEX6peroxisomal biogenesis factor 6 | Noen ganger (5–29 %) | I 1 tilstand |
| PHF6PHD finger protein 6 | Noen ganger (5–29 %) | I 1 tilstand |
| PLEKHG4pleckstrin homology and RhoGEF domain containing G4 | Noen ganger (5–29 %) | I 1 tilstand |
| PMM2phosphomannomutase 2 | Noen ganger (5–29 %) | I 1 tilstand |
| PMPCApeptidase, mitochondrial processing subunit alpha | Noen ganger (5–29 %) | I 1 tilstand |
| POLG2DNA polymerase gamma 2, accessory subunit | Noen ganger (5–29 %) | I 1 tilstand |
| POLR3ARNA polymerase III subunit A | Noen ganger (5–29 %) | I 2 tilstander |
| POLR3BRNA polymerase III subunit B | Noen ganger (5–29 %) | I 1 tilstand |
| PRF1perforin 1 | Noen ganger (5–29 %) | I 1 tilstand |
| RAB18RAB18, member RAS oncogene family | Noen ganger (5–29 %) | I 1 tilstand |
| RAB3GAP1RAB3 GTPase activating protein catalytic subunit 1 | Noen ganger (5–29 %) | I 1 tilstand |
| RAB3GAP2RAB3 GTPase activating non-catalytic protein subunit 2 | Noen ganger (5–29 %) | I 1 tilstand |
| RAD21RAD21 cohesin complex component | Noen ganger (5–29 %) | I 1 tilstand |
| RMND1required for meiotic nuclear division 1 homolog | Noen ganger (5–29 %) | I 1 tilstand |
| RNASEH1ribonuclease H1 | Noen ganger (5–29 %) | I 1 tilstand |
| RNF113Aring finger protein 113A | Noen ganger (5–29 %) | I 1 tilstand |
| RNU7-1RNA, U7 small nuclear 1 | Noen ganger (5–29 %) | I 1 tilstand |
| SAA1serum amyloid A1 | Noen ganger (5–29 %) | I 1 tilstand |
| SEPTIN9septin 9 | Noen ganger (5–29 %) | I 2 tilstander |
| SIL1SIL1 nucleotide exchange factor | Noen ganger (5–29 %) | I 1 tilstand |
| SLC25A4solute carrier family 25 member 4 | Noen ganger (5–29 %) | I 1 tilstand |
| SLC52A3solute carrier family 52 member 3 | Noen ganger (5–29 %) | I 1 tilstand |
| SMC1Astructural maintenance of chromosomes 1A | Noen ganger (5–29 %) | I 1 tilstand |
| SMC3structural maintenance of chromosomes 3 | Noen ganger (5–29 %) | I 1 tilstand |
| SMPD1sphingomyelin phosphodiesterase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| SPG21SPG21 abhydrolase domain containing, maspardin | Noen ganger (5–29 %) | I 1 tilstand |
| STX11syntaxin 11 | Noen ganger (5–29 %) | I 1 tilstand |
| STXBP2syntaxin binding protein 2 | Noen ganger (5–29 %) | I 1 tilstand |
| TARS1threonyl-tRNA synthetase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| TBC1D20TBC1 domain family member 20 | Noen ganger (5–29 %) | I 1 tilstand |
| TBC1D24TBC1 domain family member 24 | Noen ganger (5–29 %) | I 1 tilstand |
| TIMM8Atranslocase of inner mitochondrial membrane 8A | Noen ganger (5–29 %) | I 1 tilstand |
| TNFRSF1BTNF receptor superfamily member 1B | Noen ganger (5–29 %) | I 1 tilstand |
| TWNKtwinkle mtDNA helicase | Noen ganger (5–29 %) | I 1 tilstand |
| UNC13Dunc-13 homolog D | Noen ganger (5–29 %) | I 1 tilstand |
| WASWASP actin nucleation promoting factor | Noen ganger (5–29 %) | I 1 tilstand |
| WFS1wolframin ER transmembrane glycoprotein | Noen ganger (5–29 %) | I 1 tilstand |
| XPAXPA, DNA damage recognition and repair factor | Noen ganger (5–29 %) | I 1 tilstand |
| XPCXPC complex subunit, DNA damage recognition and repair factor | Noen ganger (5–29 %) | I 1 tilstand |
| ADAT3adenosine deaminase tRNA specific 3 | Sjelden (1–4%) | I 1 tilstand |
| FA2Hfatty acid 2-hydroxylase | Sjelden (1–4%) | I 1 tilstand |
| GCDHglutaryl-CoA dehydrogenase | Sjelden (1–4%) | I 1 tilstand |
| GJB2gap junction protein beta 2 | Sjelden (1–4%) | I 1 tilstand |
| GJB6gap junction protein beta 6 | Sjelden (1–4%) | I 1 tilstand |
| KIF1Ckinesin family member 1C | Sjelden (1–4%) | I 1 tilstand |
| LDB3LIM domain binding 3 | Sjelden (1–4%) | I 1 tilstand |
| NF2NF2, moesin-ezrin-radixin like (MERLIN) tumor suppressor | Sjelden (1–4%) | I 1 tilstand |
| TTBK2tau tubulin kinase 2 | Sjelden (1–4%) | I 1 tilstand |
| TTRtransthyretin | Sjelden (1–4%) | I 3 tilstander |
| AGXTalanine--glyoxylate aminotransferase | Ikke registrert | I 1 tilstand |
| ARandrogen receptor | Ikke registrert | I 1 tilstand |
| ATXN8ataxin 8 | Ikke registrert | I 1 tilstand |
| ATXN8OSATXN8 opposite strand lncRNA | Ikke registrert | I 1 tilstand |
| COX6A1cytochrome c oxidase subunit 6A1 | Ikke registrert | I 1 tilstand |
| CPOXcoproporphyrinogen oxidase | Ikke registrert | I 1 tilstand |
| DYNC1H1dynein cytoplasmic 1 heavy chain 1 | Ikke registrert | I 1 tilstand |
| GARS1glycyl-tRNA synthetase 1 | Ikke registrert | I 1 tilstand |
| GJB1gap junction protein beta 1 | Ikke registrert | I 1 tilstand |
| HARS1histidyl-tRNA synthetase 1 | Ikke registrert | I 1 tilstand |
| HK1hexokinase 1 | Ikke registrert | I 1 tilstand |
| HSPB1heat shock protein family B (small) member 1 | Ikke registrert | I 1 tilstand |
| HSPB3heat shock protein family B (small) member 3 | Ikke registrert | I 1 tilstand |
| KIF1Akinesin family member 1A | Ikke registrert | I 2 tilstander |
| KIF1Bkinesin family member 1B | Ikke registrert | I 1 tilstand |
| MAGmyelin associated glycoprotein | Ikke registrert | I 1 tilstand |
| MFFmitochondrial fission factor | Ikke registrert | I 1 tilstand |
| MGAT2alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase | Ikke registrert | I 1 tilstand |
| MPZmyelin protein zero | Ikke registrert | I 1 tilstand |
| NAGLUN-acetyl-alpha-glucosaminidase | Ikke registrert | I 1 tilstand |
| PDK3pyruvate dehydrogenase kinase 3 | Ikke registrert | I 1 tilstand |
| PPOXprotoporphyrinogen oxidase | Ikke registrert | I 1 tilstand |
| RAB7ARAB7A, member RAS oncogene family | Ikke registrert | I 1 tilstand |
| RETREG1reticulophagy regulator 1 | Ikke registrert | I 1 tilstand |
| SGPL1sphingosine-1-phosphate lyase 1 | Ikke registrert | I 1 tilstand |
| SLC5A6solute carrier family 5 member 6 | Ikke registrert | I 1 tilstand |
| SLC5A7solute carrier family 5 member 7 | Ikke registrert | I 1 tilstand |
| SUCLA2succinate-CoA ligase ADP-forming subunit beta | Ikke registrert | I 1 tilstand |
| SURF1SURF1 cytochrome c oxidase assembly factor | Ikke registrert | I 1 tilstand |
| TGM6transglutaminase 6 | Ikke registrert | I 1 tilstand |
| TPI1triosephosphate isomerase 1 | Ikke registrert | I 1 tilstand |
| TXN2thioredoxin 2 | Ikke registrert | I 1 tilstand |
| WNK1WNK lysine deficient protein kinase 1 | Ikke registrert | I 1 tilstand |
Hvor ofte dette forekommer hos personer med en av genets tilstander, oppgitt som den hyppigste forekomsten blant dem, slik Human Phenotype Ontology registrerer den. Disse sidene beskriver egenskaper og forskningen bak dem. De er ikke en diagnose, og om symptomer bør du spørre lege eller genetisk rådgiver.
Smalere egenskaper
- Peripheral axonal neuropathy144 gener
- Nerve damage causing decreased feeling and movement107 gener
- Peripheral nerve disease75 gener
- Damage to nerves that sense feeling59 gener
- Demyelinating peripheral neuropathy58 gener
- Motor polyneuropathy27 gener
- Mixed demyelinating and axonal polyneuropathy19 gener
- Progressive peripheral neuropathy5 gener
- Acute episodes of neuropathic symptoms4 gener
- Single damaged nerve2 gener
- Chronic sensorineural polyneuropathy1 gen
- Entrapment neuropathy1 gen
- Episodic peripheral neuropathy1 gen
Bredere egenskaper
Slik er informasjonen samlet
- Human Phenotype Ontology, versjon 2026-09-01: egenskapen, navnene på den, definisjonen og genene som er knyttet til den. Les mer på hpo.jax.org.
- Datautgave 2026.10.17-8666dff2.
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