Trait
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.
Summary
- Also called
- Peripheral nerve damage, Peripheral neuritis
- Body system
- Abnormality of the nervous system
Reference genomeGRCh38hg38
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Get my Genome Test271 genes linked to Peripheral neuropathy
Changes in these genes cause rare conditions in which Peripheral neuropathy is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.
| Gene | How often it is seen | Conditions |
|---|---|---|
| ACER3alkaline ceramidase 3 | Always | In 1 condition |
| AFG3L2AFG3 like matrix AAA peptidase subunit 2 | Always | In 1 condition |
| BAG3BAG cochaperone 3 | Always | In 1 condition |
| C19orf12chromosome 19 open reading frame 12 | Always | In 1 condition |
| CADM3cell adhesion molecule 3 | Always | In 1 condition |
| DARS2aspartyl-tRNA synthetase 2, mitochondrial | Always | In 1 condition |
| DMXL2Dmx like 2 | Always | In 1 condition |
| DNAJC3DnaJ heat shock protein family (Hsp40) member C3 | Always | In 1 condition |
| EEFSECeukaryotic elongation factor, selenocysteine-tRNA specific | Always | In 1 condition |
| EGR2early growth response 2 | Always | In 2 conditions |
| GDAP1ganglioside induced differentiation associated protein 1 | Always | In 1 condition |
| GTPBP2GTP binding protein 2 | Always | In 1 condition |
| HSPB8heat shock protein family B (small) member 8 | Always | In 1 condition |
| IARS2isoleucyl-tRNA synthetase 2, mitochondrial | Always | In 3 conditions |
| INF2inverted formin 2 | Always | In 1 condition |
| ITPR3inositol 1,4,5-trisphosphate receptor type 3 | Always | In 1 condition |
| MFN2mitofusin 2 | Always | In 2 conditions |
| NDC1NDC1 transmembrane nucleoporin | Always | In 1 condition |
| NGFnerve growth factor | Always | In 1 condition |
| OPA1OPA1 mitochondrial dynamin like GTPase | Always | In 3 conditions |
| PDSS1decaprenyl diphosphate synthase subunit 1 | Always | In 1 condition |
| PEX5peroxisomal biogenesis factor 5 | Always | In 1 condition |
| PNKPpolynucleotide kinase 3'-phosphatase | Always | In 2 conditions |
| POLGDNA polymerase gamma, catalytic subunit | Always | In 5 conditions |
| PRPS1phosphoribosyl pyrophosphate synthetase 1 | Always | In 6 conditions |
| PSAPprosaposin | Always | In 2 conditions |
| REEP1receptor accessory protein 1 | Always | In 1 condition |
| RFC1replication factor C subunit 1 | Always | In 1 condition |
| RFC4replication factor C subunit 4 | Always | In 1 condition |
| SCO2synthesis of cytochrome C oxidase 2 | Always | In 1 condition |
| SCP2sterol carrier protein 2 | Always | In 1 condition |
| SPTAN1spectrin alpha, non-erythrocytic 1 | Always | In 1 condition |
| TYMPthymidine phosphorylase | Always | In 2 conditions |
| ABCD1ATP binding cassette subfamily D member 1 | Very often (80–99%) | In 2 conditions |
| AIFM1apoptosis inducing factor mitochondria associated 1 | Very often (80–99%) | In 1 condition |
| AP1B1adaptor related protein complex 1 subunit beta 1 | Very often (80–99%) | In 1 condition |
| AP1S1adaptor related protein complex 1 subunit sigma 1 | Very often (80–99%) | In 2 conditions |
| APTXaprataxin | Very often (80–99%) | In 1 condition |
| ATXN1ataxin 1 | Very often (80–99%) | In 2 conditions |
| ATXN3ataxin 3 | Very often (80–99%) | In 2 conditions |
Show 231 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| CCT5chaperonin containing TCP1 subunit 5 | Very often (80–99%) | In 1 condition |
| ELP1elongator acetyltransferase complex subunit 1 | Very often (80–99%) | In 1 condition |
| GBE11,4-alpha-glucan branching enzyme 1 | Very often (80–99%) | In 1 condition |
| GCLCglutamate-cysteine ligase catalytic subunit | Very often (80–99%) | In 1 condition |
| LYSTlysosomal trafficking regulator | Very often (80–99%) | In 2 conditions |
| MYOTmyotilin | Very often (80–99%) | In 1 condition |
| PEX7peroxisomal biogenesis factor 7 | Very often (80–99%) | In 1 condition |
| PHYHphytanoyl-CoA 2-hydroxylase | Very often (80–99%) | In 1 condition |
| PMP22peripheral myelin protein 22 | Very often (80–99%) | In 3 conditions |
| SCN10Asodium voltage-gated channel alpha subunit 10 | Very often (80–99%) | In 1 condition |
| SCN11Asodium voltage-gated channel alpha subunit 11 | Very often (80–99%) | In 1 condition |
| SCN9Asodium voltage-gated channel alpha subunit 9 | Very often (80–99%) | In 2 conditions |
| SOX10SRY-box transcription factor 10 | Very often (80–99%) | In 1 condition |
| TFGtrafficking from ER to golgi regulator | Very often (80–99%) | In 2 conditions |
| TTPAalpha tocopherol transfer protein | Very often (80–99%) | In 1 condition |
| ALADaminolevulinate dehydratase | Often (30–79%) | In 1 condition |
| ATP5F1AATP synthase F1 subunit alpha | Often (30–79%) | In 1 condition |
| ATP5F1DATP synthase F1 subunit delta | Often (30–79%) | In 1 condition |
| ATP5F1EATP synthase F1 subunit epsilon | Often (30–79%) | In 2 conditions |
| ATP5MKATP synthase membrane subunit k | Often (30–79%) | In 1 condition |
| ATP5POATP synthase peripheral stalk subunit OSCP | Often (30–79%) | In 1 condition |
| ATPAF2ATP synthase mitochondrial F1 complex assembly factor 2 | Often (30–79%) | In 1 condition |
| BORCS5BLOC-1 related complex subunit 5 | Often (30–79%) | In 1 condition |
| CAPN1calpain 1 | Often (30–79%) | In 2 conditions |
| CTLA4cytotoxic T-lymphocyte associated protein 4 | Often (30–79%) | In 2 conditions |
| CYP27A1cytochrome P450 family 27 subfamily A member 1 | Often (30–79%) | In 2 conditions |
| DCAF17DDB1 and CUL4 associated factor 17 | Often (30–79%) | In 1 condition |
| ELOVL5ELOVL fatty acid elongase 5 | Often (30–79%) | In 1 condition |
| EMILIN1elastin microfibril interfacer 1 | Often (30–79%) | In 1 condition |
| ERBB3erb-b2 receptor tyrosine kinase 3 | Often (30–79%) | In 1 condition |
| ERCC6ERCC excision repair 6, chromatin remodeling factor | Often (30–79%) | In 3 conditions |
| ERCC8ERCC excision repair 8, CSA ubiquitin ligase complex subunit | Often (30–79%) | In 1 condition |
| FMR1fragile X messenger ribonucleoprotein 1 | Often (30–79%) | In 2 conditions |
| GALCgalactosylceramidase | Often (30–79%) | In 3 conditions |
| HADHAhydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha | Often (30–79%) | In 3 conditions |
| HADHBhydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta | Often (30–79%) | In 2 conditions |
| HLA-DPA1major histocompatibility complex, class II, DP alpha 1 | Often (30–79%) | In 1 condition |
| HLA-DPB1major histocompatibility complex, class II, DP beta 1 | Often (30–79%) | In 1 condition |
| HMBShydroxymethylbilane synthase | Often (30–79%) | In 1 condition |
| LETM1leucine zipper and EF-hand containing transmembrane protein 1 | Often (30–79%) | In 1 condition |
| LIG3DNA ligase 3 | Often (30–79%) | In 1 condition |
| LRPPRCleucine rich pentatricopeptide repeat containing | Often (30–79%) | In 1 condition |
| MARS1methionyl-tRNA synthetase 1 | Often (30–79%) | In 1 condition |
| MT-ATP6mitochondrially encoded ATP synthase membrane subunit 6 | Often (30–79%) | In 2 conditions |
| MT-ATP8mitochondrially encoded ATP synthase membrane subunit 8 | Often (30–79%) | In 1 condition |
| MT-CO1mitochondrially encoded cytochrome c oxidase I | Often (30–79%) | In 2 conditions |
| MT-CO2mitochondrially encoded cytochrome c oxidase II | Often (30–79%) | In 1 condition |
| MT-CO3mitochondrially encoded cytochrome c oxidase III | Often (30–79%) | In 2 conditions |
| MT-ND1mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 | Often (30–79%) | In 2 conditions |
| MT-ND4mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 | Often (30–79%) | In 2 conditions |
| MT-ND5mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 | Often (30–79%) | In 2 conditions |
| MT-ND6mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 | Often (30–79%) | In 2 conditions |
| MT-TFmitochondrially encoded tRNA-Phe (UUU/C) | Often (30–79%) | In 1 condition |
| MT-THmitochondrially encoded tRNA-His (CAU/C) | Often (30–79%) | In 1 condition |
| MT-TL1mitochondrially encoded tRNA-Leu (UUA/G) 1 | Often (30–79%) | In 1 condition |
| MT-TQmitochondrially encoded tRNA-Gln (CAA/G) | Often (30–79%) | In 1 condition |
| MT-TS1mitochondrially encoded tRNA-Ser (UCN) 1 | Often (30–79%) | In 1 condition |
| MT-TS2mitochondrially encoded tRNA-Ser (AGU/C) 2 | Often (30–79%) | In 1 condition |
| MT-TWmitochondrially encoded tRNA-Trp (UGA/G) | Often (30–79%) | In 1 condition |
| MTHFRmethylenetetrahydrofolate reductase | Often (30–79%) | In 1 condition |
| MTRFRmitochondrial translation release factor in rescue | Often (30–79%) | In 1 condition |
| MYH14myosin heavy chain 14 | Often (30–79%) | In 2 conditions |
| NAGAalpha-N-acetylgalactosaminidase | Often (30–79%) | In 2 conditions |
| NARS1asparaginyl-tRNA synthetase 1 | Often (30–79%) | In 2 conditions |
| NGLY1N-glycanase 1 | Often (30–79%) | In 1 condition |
| PDE4Dphosphodiesterase 4D | Often (30–79%) | In 1 condition |
| PLA2G6phospholipase A2 group VI | Often (30–79%) | In 1 condition |
| PNPLA6patatin like domain 6, lysophospholipase | Often (30–79%) | In 2 conditions |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Often (30–79%) | In 1 condition |
| PRTN3proteinase 3 | Often (30–79%) | In 1 condition |
| PTPN22protein tyrosine phosphatase non-receptor type 22 | Often (30–79%) | In 2 conditions |
| RAI1retinoic acid induced 1 | Often (30–79%) | In 2 conditions |
| RRM1ribonucleotide reductase catalytic subunit M1 | Often (30–79%) | In 1 condition |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Often (30–79%) | In 2 conditions |
| SACSsacsin molecular chaperone | Often (30–79%) | In 1 condition |
| SCYL1SCY1 like pseudokinase 1 | Often (30–79%) | In 1 condition |
| SLC12A6solute carrier family 12 member 6 | Often (30–79%) | In 1 condition |
| SLC30A10solute carrier family 30 member 10 | Often (30–79%) | In 1 condition |
| SLC46A1solute carrier family 46 member 1 | Often (30–79%) | In 2 conditions |
| SNAP29synaptosome associated protein 29 | Often (30–79%) | In 2 conditions |
| TDP1tyrosyl-DNA phosphodiesterase 1 | Often (30–79%) | In 1 condition |
| TIMMDC1translocase of inner mitochondrial membrane domain containing 1 | Often (30–79%) | In 1 condition |
| TK2thymidine kinase 2 | Often (30–79%) | In 1 condition |
| TNXBtenascin XB | Often (30–79%) | In 1 condition |
| TOP3ADNA topoisomerase III alpha | Often (30–79%) | In 1 condition |
| TRMT5tRNA methyltransferase 5 | Often (30–79%) | In 1 condition |
| ZFRzinc finger RNA binding protein | Often (30–79%) | In 1 condition |
| AARS1alanyl-tRNA synthetase 1 | Sometimes (5–29%) | In 2 conditions |
| ABCC8ATP binding cassette subfamily C member 8 | Sometimes (5–29%) | In 1 condition |
| ADA2adenosine deaminase 2 | Sometimes (5–29%) | In 2 conditions |
| ALDH4A1aldehyde dehydrogenase 4 family member A1 | Sometimes (5–29%) | In 1 condition |
| AP5Z1adaptor related protein complex 5 subunit zeta 1 | Sometimes (5–29%) | In 2 conditions |
| ATL1atlastin GTPase 1 | Sometimes (5–29%) | In 2 conditions |
| ATP6V1B2ATPase H+ transporting V1 subunit B2 | Sometimes (5–29%) | In 1 condition |
| BMP6bone morphogenetic protein 6 | Sometimes (5–29%) | In 1 condition |
| BRD4bromodomain containing 4 | Sometimes (5–29%) | In 1 condition |
| BTNL2butyrophilin like 2 | Sometimes (5–29%) | In 1 condition |
| CARS1cysteinyl-tRNA synthetase 1 | Sometimes (5–29%) | In 1 condition |
| CBLIFcobalamin binding intrinsic factor | Sometimes (5–29%) | In 1 condition |
| CCND1cyclin D1 | Sometimes (5–29%) | In 1 condition |
| CD28CD28 molecule | Sometimes (5–29%) | In 1 condition |
| CD4CD4 molecule | Sometimes (5–29%) | In 1 condition |
| CISD2CDGSH iron sulfur domain 2 | Sometimes (5–29%) | In 1 condition |
| DBR1debranching RNA lariats 1 | Sometimes (5–29%) | In 1 condition |
| DDB2damage specific DNA binding protein 2 | Sometimes (5–29%) | In 1 condition |
| DNAJC30DnaJ heat shock protein family (Hsp40) member C30 | Sometimes (5–29%) | In 1 condition |
| DNASE1L3deoxyribonuclease 1L3 | Sometimes (5–29%) | In 1 condition |
| DNMT1DNA methyltransferase 1 | Sometimes (5–29%) | In 1 condition |
| DPM1dolichyl-phosphate mannosyltransferase subunit 1, catalytic | Sometimes (5–29%) | In 1 condition |
| DSTYKdual serine/threonine and tyrosine protein kinase | Sometimes (5–29%) | In 1 condition |
| ERCC1ERCC excision repair 1, endonuclease non-catalytic subunit | Sometimes (5–29%) | In 1 condition |
| ERCC2ERCC excision repair 2, TFIIH core complex helicase subunit | Sometimes (5–29%) | In 3 conditions |
| ERCC3ERCC excision repair 3, TFIIH core complex helicase subunit | Sometimes (5–29%) | In 2 conditions |
| ERCC4ERCC excision repair 4, endonuclease catalytic subunit | Sometimes (5–29%) | In 1 condition |
| ERCC5ERCC excision repair 5, endonuclease | Sometimes (5–29%) | In 2 conditions |
| FBN1fibrillin 1 | Sometimes (5–29%) | In 2 conditions |
| FLNCfilamin C | Sometimes (5–29%) | In 1 condition |
| GTF2E2general transcription factor IIE subunit 2 | Sometimes (5–29%) | In 1 condition |
| GTF2H5general transcription factor IIH subunit 5 | Sometimes (5–29%) | In 1 condition |
| GUK1guanylate kinase 1 | Sometimes (5–29%) | In 1 condition |
| HADHhydroxyacyl-CoA dehydrogenase | Sometimes (5–29%) | In 1 condition |
| HDAC8histone deacetylase 8 | Sometimes (5–29%) | In 1 condition |
| HFEhomeostatic iron regulator | Sometimes (5–29%) | In 1 condition |
| HLA-Bmajor histocompatibility complex, class I, B | Sometimes (5–29%) | In 1 condition |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Sometimes (5–29%) | In 2 conditions |
| HSD3B7hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7 | Sometimes (5–29%) | In 1 condition |
| INSRinsulin receptor | Sometimes (5–29%) | In 1 condition |
| IRF4interferon regulatory factor 4 | Sometimes (5–29%) | In 1 condition |
| KCNJ11potassium inwardly rectifying channel subfamily J member 11 | Sometimes (5–29%) | In 1 condition |
| MAU2MAU2 sister chromatid cohesion factor | Sometimes (5–29%) | In 1 condition |
| MPC1mitochondrial pyruvate carrier 1 | Sometimes (5–29%) | In 1 condition |
| MPLKIPM-phase specific PLK1 interacting protein | Sometimes (5–29%) | In 1 condition |
| MPV17mitochondrial inner membrane protein MPV17 | Sometimes (5–29%) | In 1 condition |
| MT-CYBmitochondrially encoded cytochrome b | Sometimes (5–29%) | In 1 condition |
| MT-ND2mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 | Sometimes (5–29%) | In 1 condition |
| MT-ND4Lmitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L | Sometimes (5–29%) | In 1 condition |
| MT-TKmitochondrially encoded tRNA-Lys (AAA/G) | Sometimes (5–29%) | In 1 condition |
| MTRR5-methyltetrahydrofolate-homocysteine methyltransferase reductase | Sometimes (5–29%) | In 1 condition |
| MYD88MYD88 innate immune signal transduction adaptor | Sometimes (5–29%) | In 1 condition |
| NARS2asparaginyl-tRNA synthetase 2, mitochondrial | Sometimes (5–29%) | In 1 condition |
| NDUFS2NADH:ubiquinone oxidoreductase core subunit S2 | Sometimes (5–29%) | In 1 condition |
| NEFLneurofilament light chain | Sometimes (5–29%) | In 1 condition |
| NFU1NFU1 iron-sulfur cluster scaffold | Sometimes (5–29%) | In 1 condition |
| NIPBLNIPBL cohesin loading factor | Sometimes (5–29%) | In 1 condition |
| NOTCH2notch receptor 2 | Sometimes (5–29%) | In 1 condition |
| NOTCH3notch receptor 3 | Sometimes (5–29%) | In 1 condition |
| P4HA2prolyl 4-hydroxylase subunit alpha 2 | Sometimes (5–29%) | In 1 condition |
| PEX1peroxisomal biogenesis factor 1 | Sometimes (5–29%) | In 1 condition |
| PEX16peroxisomal biogenesis factor 16 | Sometimes (5–29%) | In 1 condition |
| PEX6peroxisomal biogenesis factor 6 | Sometimes (5–29%) | In 1 condition |
| PHF6PHD finger protein 6 | Sometimes (5–29%) | In 1 condition |
| PLEKHG4pleckstrin homology and RhoGEF domain containing G4 | Sometimes (5–29%) | In 1 condition |
| PMM2phosphomannomutase 2 | Sometimes (5–29%) | In 1 condition |
| PMPCApeptidase, mitochondrial processing subunit alpha | Sometimes (5–29%) | In 1 condition |
| POLG2DNA polymerase gamma 2, accessory subunit | Sometimes (5–29%) | In 1 condition |
| POLR3ARNA polymerase III subunit A | Sometimes (5–29%) | In 2 conditions |
| POLR3BRNA polymerase III subunit B | Sometimes (5–29%) | In 1 condition |
| PRF1perforin 1 | Sometimes (5–29%) | In 1 condition |
| RAB18RAB18, member RAS oncogene family | Sometimes (5–29%) | In 1 condition |
| RAB3GAP1RAB3 GTPase activating protein catalytic subunit 1 | Sometimes (5–29%) | In 1 condition |
| RAB3GAP2RAB3 GTPase activating non-catalytic protein subunit 2 | Sometimes (5–29%) | In 1 condition |
| RAD21RAD21 cohesin complex component | Sometimes (5–29%) | In 1 condition |
| RMND1required for meiotic nuclear division 1 homolog | Sometimes (5–29%) | In 1 condition |
| RNASEH1ribonuclease H1 | Sometimes (5–29%) | In 1 condition |
| RNF113Aring finger protein 113A | Sometimes (5–29%) | In 1 condition |
| RNU7-1RNA, U7 small nuclear 1 | Sometimes (5–29%) | In 1 condition |
| SAA1serum amyloid A1 | Sometimes (5–29%) | In 1 condition |
| SEPTIN9septin 9 | Sometimes (5–29%) | In 2 conditions |
| SIL1SIL1 nucleotide exchange factor | Sometimes (5–29%) | In 1 condition |
| SLC25A4solute carrier family 25 member 4 | Sometimes (5–29%) | In 1 condition |
| SLC52A3solute carrier family 52 member 3 | Sometimes (5–29%) | In 1 condition |
| SMC1Astructural maintenance of chromosomes 1A | Sometimes (5–29%) | In 1 condition |
| SMC3structural maintenance of chromosomes 3 | Sometimes (5–29%) | In 1 condition |
| SMPD1sphingomyelin phosphodiesterase 1 | Sometimes (5–29%) | In 1 condition |
| SPG21SPG21 abhydrolase domain containing, maspardin | Sometimes (5–29%) | In 1 condition |
| STX11syntaxin 11 | Sometimes (5–29%) | In 1 condition |
| STXBP2syntaxin binding protein 2 | Sometimes (5–29%) | In 1 condition |
| TARS1threonyl-tRNA synthetase 1 | Sometimes (5–29%) | In 1 condition |
| TBC1D20TBC1 domain family member 20 | Sometimes (5–29%) | In 1 condition |
| TBC1D24TBC1 domain family member 24 | Sometimes (5–29%) | In 1 condition |
| TIMM8Atranslocase of inner mitochondrial membrane 8A | Sometimes (5–29%) | In 1 condition |
| TNFRSF1BTNF receptor superfamily member 1B | Sometimes (5–29%) | In 1 condition |
| TWNKtwinkle mtDNA helicase | Sometimes (5–29%) | In 1 condition |
| UNC13Dunc-13 homolog D | Sometimes (5–29%) | In 1 condition |
| WASWASP actin nucleation promoting factor | Sometimes (5–29%) | In 1 condition |
| WFS1wolframin ER transmembrane glycoprotein | Sometimes (5–29%) | In 1 condition |
| XPAXPA, DNA damage recognition and repair factor | Sometimes (5–29%) | In 1 condition |
| XPCXPC complex subunit, DNA damage recognition and repair factor | Sometimes (5–29%) | In 1 condition |
| ADAT3adenosine deaminase tRNA specific 3 | Rarely (1–4%) | In 1 condition |
| FA2Hfatty acid 2-hydroxylase | Rarely (1–4%) | In 1 condition |
| GCDHglutaryl-CoA dehydrogenase | Rarely (1–4%) | In 1 condition |
| GJB2gap junction protein beta 2 | Rarely (1–4%) | In 1 condition |
| GJB6gap junction protein beta 6 | Rarely (1–4%) | In 1 condition |
| KIF1Ckinesin family member 1C | Rarely (1–4%) | In 1 condition |
| LDB3LIM domain binding 3 | Rarely (1–4%) | In 1 condition |
| NF2NF2, moesin-ezrin-radixin like (MERLIN) tumor suppressor | Rarely (1–4%) | In 1 condition |
| TTBK2tau tubulin kinase 2 | Rarely (1–4%) | In 1 condition |
| TTRtransthyretin | Rarely (1–4%) | In 3 conditions |
| AGXTalanine--glyoxylate aminotransferase | Not recorded | In 1 condition |
| ARandrogen receptor | Not recorded | In 1 condition |
| ATXN8ataxin 8 | Not recorded | In 1 condition |
| ATXN8OSATXN8 opposite strand lncRNA | Not recorded | In 1 condition |
| COX6A1cytochrome c oxidase subunit 6A1 | Not recorded | In 1 condition |
| CPOXcoproporphyrinogen oxidase | Not recorded | In 1 condition |
| DYNC1H1dynein cytoplasmic 1 heavy chain 1 | Not recorded | In 1 condition |
| GARS1glycyl-tRNA synthetase 1 | Not recorded | In 1 condition |
| GJB1gap junction protein beta 1 | Not recorded | In 1 condition |
| HARS1histidyl-tRNA synthetase 1 | Not recorded | In 1 condition |
| HK1hexokinase 1 | Not recorded | In 1 condition |
| HSPB1heat shock protein family B (small) member 1 | Not recorded | In 1 condition |
| HSPB3heat shock protein family B (small) member 3 | Not recorded | In 1 condition |
| KIF1Akinesin family member 1A | Not recorded | In 2 conditions |
| KIF1Bkinesin family member 1B | Not recorded | In 1 condition |
| MAGmyelin associated glycoprotein | Not recorded | In 1 condition |
| MFFmitochondrial fission factor | Not recorded | In 1 condition |
| MGAT2alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase | Not recorded | In 1 condition |
| MPZmyelin protein zero | Not recorded | In 1 condition |
| NAGLUN-acetyl-alpha-glucosaminidase | Not recorded | In 1 condition |
| PDK3pyruvate dehydrogenase kinase 3 | Not recorded | In 1 condition |
| PPOXprotoporphyrinogen oxidase | Not recorded | In 1 condition |
| RAB7ARAB7A, member RAS oncogene family | Not recorded | In 1 condition |
| RETREG1reticulophagy regulator 1 | Not recorded | In 1 condition |
| SGPL1sphingosine-1-phosphate lyase 1 | Not recorded | In 1 condition |
| SLC5A6solute carrier family 5 member 6 | Not recorded | In 1 condition |
| SLC5A7solute carrier family 5 member 7 | Not recorded | In 1 condition |
| SUCLA2succinate-CoA ligase ADP-forming subunit beta | Not recorded | In 1 condition |
| SURF1SURF1 cytochrome c oxidase assembly factor | Not recorded | In 1 condition |
| TGM6transglutaminase 6 | Not recorded | In 1 condition |
| TPI1triosephosphate isomerase 1 | Not recorded | In 1 condition |
| TXN2thioredoxin 2 | Not recorded | In 1 condition |
| WNK1WNK lysine deficient protein kinase 1 | Not recorded | In 1 condition |
How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.
Narrower traits
- Peripheral axonal neuropathy144 genes
- Nerve damage causing decreased feeling and movement107 genes
- Peripheral nerve disease75 genes
- Damage to nerves that sense feeling59 genes
- Demyelinating peripheral neuropathy58 genes
- Motor polyneuropathy27 genes
- Mixed demyelinating and axonal polyneuropathy19 genes
- Progressive peripheral neuropathy5 genes
- Acute episodes of neuropathic symptoms4 genes
- Single damaged nerve2 genes
- Chronic sensorineural polyneuropathy1 gene
- Entrapment neuropathy1 gene
- Episodic peripheral neuropathy1 gene
Broader traits
Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
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