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Abnormality of balance
Klinisk navn: Gait imbalance
Resumé
- Også kaldet
- Abnormality of equilibrium, Imbalanced walk
- Kropssystem
- Abnormality of the nervous system
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Tilføj .json til sidens adresse, eller bed om application/json, for at læse den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/gait-imbalance.json"
page <- fromJSON(url)
page$trait$nameAbnormality of balanceHP:0002141
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Læs de gener, der er knyttet til Abnormality of balance, og resten af dit genom, med én test.
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Bestil min Genome Test49 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.
- Parkinson DiseaseReads 10 of these genesFBXO7MAPTDNAJC6LRRK2PARK7PINK1About this report →
- Usher SyndromeReads 8 of these genesCDH23MYO7APCDH15USH1CUSH1GADGRV1About this report →
- 3-Methylglutaconic Aciduria Type 8 (HTRA2)Reads 1 of these genesHTRA2About this report →
- Angelman SyndromeReads 1 of these genesUBE3AAbout this report →
Show 45 more reports
- FDXR-Related Mitochondrial DisorderReads 1 of these genesFDXRAbout this report →
- Friedreich AtaxiaReads 1 of these genesFXNAbout this report →
- Hereditary Neuropathy with Liability to Pressure Palsies (HNPP)Reads 1 of these genesPMP22About this report →
- Huntington DiseaseReads 1 of these genesHTTAbout this report →
- Radio-Tartaglia SyndromeReads 1 of these genesSPENAbout this report →
- You-Hoover-Fong Syndrome (TELO2)Reads 1 of these genesTELO2About this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 5 of these genesALS2SPTLC1SPTLC2SETXVCPAbout this report →
- Inherited Neurodegenerative DisordersReads 17 of these genesCAPN1MAPTALS2ATL1ERLIN2FXNAbout this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 4 of these genesATL1ATL3SPTLC1SPTLC2About this report →
- Rare Hereditary Peripheral NeuropathiesReads 12 of these genesFDXRMPV17ATL1ATL3SPTLC1SPTLC2About this report →
- Hearing Loss and DeafnessReads 7 of these genesCDH23ESPNMYO7APCDH15USH1CPDZD7About this report →
- Riboflavin Transporter DeficiencyReads 1 of these genesSLC52A3About this report →
- Hereditary Spastic ParaplegiaReads 5 of these genesCAPN1ATL1ERLIN2SPG7UCHL1About this report →
- Charcot-Marie-Tooth DiseaseReads 5 of these genesMPV17SETXVCPHK1PMP22About this report →
- Frontotemporal DementiaReads 2 of these genesMAPTVCPAbout this report →
- Primary Mitochondrial DiseaseReads 6 of these genesMPV17DNAJC30ATP5F1DNDUFA1RNASEH1RRM2BAbout this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 3 of these genesTTBK2ATXN10ATXN1About this report →
- GalactosemiaReads 1 of these genesGALTAbout this report →
- Distal MyopathiesReads 2 of these genesFLNCVCPAbout this report →
- Bardet-Biedl and Alström SyndromesReads 2 of these genesARL6BBS1About this report →
- Chronic Granulomatous DiseaseReads 1 of these genesNCF1About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 3 of these genesFXNGDAP2SETXAbout this report →
- Oculocutaneous AlbinismReads 1 of these genesOCA2About this report →
- Pyruvate Kinase Deficiency and Other Red Cell Enzyme DisordersReads 1 of these genesHK1About this report →
- Retinitis PigmentosaReads 3 of these genesHK1USH2AARL6About this report →
- Intellectual DisabilityReads 5 of these genesKAT6APIGGTAF1CHD4DEAF1About this report →
- HyperinsulinismReads 1 of these genesHK1About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesELNAbout this report →
- Myofibrillar MyopathiesReads 1 of these genesFLNCAbout this report →
- Complex Cortical Dysplasia and Frontoparietal PolymicrogyriaReads 1 of these genesADGRG1About this report →
- Cutis LaxaReads 1 of these genesELNAbout this report →
- GPI Anchor Biosynthesis DefectsReads 1 of these genesPIGGAbout this report →
- Syndromic Complex Neurodevelopmental DisorderReads 1 of these genesPAN2About this report →
- Syndromic CraniosynostosisReads 1 of these genesKAT6AAbout this report →
- Nephrotic SyndromeReads 1 of these genesPODXLAbout this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesTAF1About this report →
- DNA Repair DiseaseReads 1 of these genesSETXAbout this report →
- Male InfertilityReads 1 of these genesFKBP6About this report →
- Dilated CardiomyopathyReads 1 of these genesFLNCAbout this report →
- Female InfertilityReads 1 of these genesGALTAbout this report →
- Hypertrophic CardiomyopathyReads 1 of these genesFLNCAbout this report →
- Leigh SyndromeReads 1 of these genesNDUFA1About this report →
- Congenital Disorders of GlycosylationReads 1 of these genesPIGGAbout this report →
- Epilepsy (Full Panel)Reads 1 of these genesSYNJ1About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesNCF1About this report →
Læs de gener, der er knyttet til Abnormality of balance, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test91 gener knyttet til Abnormality of balance
Ændringer i disse gener forårsager sjældne tilstande, hvor Abnormality of balance ses. De fleste med dette træk har ingen af disse tilstande, og et gen på denne liste siger intet om nogens eget genom.
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| ATXN7L3ataxin 7 like 3 | Altid | I 1 tilstand |
| CAPN1calpain 1 | Altid | I 1 tilstand |
| FBXO7F-box protein 7 | Altid | I 1 tilstand |
| FDXRferredoxin reductase | Altid | I 1 tilstand |
| KAT6Alysine acetyltransferase 6A | Altid | I 1 tilstand |
| MAPTmicrotubule associated protein tau | Altid | I 3 tilstande |
| MAU2MAU2 sister chromatid cohesion factor | Altid | I 1 tilstand |
| MPV17mitochondrial inner membrane protein MPV17 | Altid | I 1 tilstand |
| PAN2poly(A) specific ribonuclease subunit PAN2 | Altid | I 1 tilstand |
| PPP2R5Cprotein phosphatase 2 regulatory subunit B'gamma | Altid | I 1 tilstand |
| ALS2alsin Rho guanine nucleotide exchange factor ALS2 | Meget ofte (80–99 %) | I 1 tilstand |
| ATL1atlastin GTPase 1 | Meget ofte (80–99 %) | I 1 tilstand |
| ATL3atlastin GTPase 3 | Meget ofte (80–99 %) | I 1 tilstand |
| BAZ1Bbromodomain adjacent to zinc finger domain 1B | Meget ofte (80–99 %) | I 1 tilstand |
| BUD23BUD23 rRNA methyltransferase and ribosome maturation factor | Meget ofte (80–99 %) | I 1 tilstand |
| CLIP2CAP-Gly domain containing linker protein 2 | Meget ofte (80–99 %) | I 1 tilstand |
| DNAJC30DnaJ heat shock protein family (Hsp40) member C30 | Meget ofte (80–99 %) | I 1 tilstand |
| EIF4Heukaryotic translation initiation factor 4H | Meget ofte (80–99 %) | I 1 tilstand |
| ELNelastin | Meget ofte (80–99 %) | I 2 tilstande |
| ERLIN2ER lipid raft associated 2 | Meget ofte (80–99 %) | I 1 tilstand |
| FKBP6FKBP prolyl isomerase family member 6 (inactive) | Meget ofte (80–99 %) | I 1 tilstand |
| FXNfrataxin | Meget ofte (80–99 %) | I 1 tilstand |
| GTF2Igeneral transcription factor IIi | Meget ofte (80–99 %) | I 1 tilstand |
| GTF2IRD1GTF2I repeat domain containing 1 | Meget ofte (80–99 %) | I 1 tilstand |
| GTF2IRD2GTF2I repeat domain containing 2 | Meget ofte (80–99 %) | I 1 tilstand |
| LIMK1LIM domain kinase 1 | Meget ofte (80–99 %) | I 1 tilstand |
| METTL27methyltransferase like 27 | Meget ofte (80–99 %) | I 1 tilstand |
| NCF1neutrophil cytosolic factor 1 | Meget ofte (80–99 %) | I 1 tilstand |
| RFC2replication factor C subunit 2 | Meget ofte (80–99 %) | I 1 tilstand |
| SPTLC1serine palmitoyltransferase long chain base subunit 1 | Meget ofte (80–99 %) | I 1 tilstand |
| SPTLC2serine palmitoyltransferase long chain base subunit 2 | Meget ofte (80–99 %) | I 1 tilstand |
| STX1Asyntaxin 1A | Meget ofte (80–99 %) | I 1 tilstand |
| TBL2transducin beta like 2 | Meget ofte (80–99 %) | I 1 tilstand |
| TELO2telomere maintenance 2 | Meget ofte (80–99 %) | I 1 tilstand |
| TMEM270transmembrane protein 270 | Meget ofte (80–99 %) | I 1 tilstand |
| TTBK2tau tubulin kinase 2 | Meget ofte (80–99 %) | I 2 tilstande |
| VPS37DVPS37D subunit of ESCRT-I | Meget ofte (80–99 %) | I 1 tilstand |
| ADGRG1adhesion G protein-coupled receptor G1 | Ofte (30–79 %) | I 1 tilstand |
| ATP5F1DATP synthase F1 subunit delta | Ofte (30–79 %) | I 1 tilstand |
| ATXN10ataxin 10 | Ofte (30–79 %) | I 1 tilstand |
Vis 51 gener mere
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| CDH23cadherin related 23 | Ofte (30–79 %) | I 1 tilstand |
| ELFN1extracellular leucine rich repeat and fibronectin type III domain containing 1 | Ofte (30–79 %) | I 1 tilstand |
| ESPNespin | Ofte (30–79 %) | I 1 tilstand |
| FLNCfilamin C | Ofte (30–79 %) | I 1 tilstand |
| GDAP2ganglioside induced differentiation associated protein 2 | Ofte (30–79 %) | I 1 tilstand |
| HTThuntingtin | Ofte (30–79 %) | I 1 tilstand |
| MLXIPLMLX interacting protein like | Ofte (30–79 %) | I 1 tilstand |
| MYO7Amyosin VIIA | Ofte (30–79 %) | I 2 tilstande |
| NDUFA1NADH:ubiquinone oxidoreductase subunit A1 | Ofte (30–79 %) | I 1 tilstand |
| PCDH15protocadherin related 15 | Ofte (30–79 %) | I 1 tilstand |
| PIGGphosphatidylinositol glycan anchor biosynthesis class G (EMM blood group) | Ofte (30–79 %) | I 1 tilstand |
| PIK3R5phosphoinositide-3-kinase regulatory subunit 5 | Ofte (30–79 %) | I 1 tilstand |
| SETXsenataxin | Ofte (30–79 %) | I 1 tilstand |
| SLC2A3solute carrier family 2 member 3 | Ofte (30–79 %) | I 1 tilstand |
| SPENspen family transcriptional repressor | Ofte (30–79 %) | I 1 tilstand |
| SPG7SPG7 matrix AAA peptidase subunit, paraplegin | Ofte (30–79 %) | I 1 tilstand |
| TAF1TATA-box binding protein associated factor 1 | Ofte (30–79 %) | I 1 tilstand |
| USH1CUSH1 protein network component harmonin | Ofte (30–79 %) | I 1 tilstand |
| USH1GUSH1 protein network component sans | Ofte (30–79 %) | I 1 tilstand |
| VCPvalosin containing protein | Ofte (30–79 %) | I 1 tilstand |
| ADGRV1adhesion G protein-coupled receptor V1 | Nogle gange (5–29 %) | I 1 tilstand |
| ATXN1ataxin 1 | Nogle gange (5–29 %) | I 1 tilstand |
| BCAS3BCAS3 microtubule associated cell migration factor | Nogle gange (5–29 %) | I 1 tilstand |
| CHD4chromodomain helicase DNA binding protein 4 | Nogle gange (5–29 %) | I 1 tilstand |
| DEAF1DEAF1 transcription factor | Nogle gange (5–29 %) | I 1 tilstand |
| DNAJC6DnaJ heat shock protein family (Hsp40) member C6 | Nogle gange (5–29 %) | I 1 tilstand |
| GALTgalactose-1-phosphate uridylyltransferase | Nogle gange (5–29 %) | I 1 tilstand |
| HK1hexokinase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| HTRA2HtrA serine peptidase 2 | Nogle gange (5–29 %) | I 1 tilstand |
| LRRK2leucine rich repeat kinase 2 | Nogle gange (5–29 %) | I 1 tilstand |
| OCA2OCA2 melanosomal transmembrane protein | Nogle gange (5–29 %) | I 1 tilstand |
| PARK7Parkinsonism associated deglycase | Nogle gange (5–29 %) | I 1 tilstand |
| PDZD7PDZ domain containing 7 | Nogle gange (5–29 %) | I 1 tilstand |
| PINK1PTEN induced kinase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| PMP22peripheral myelin protein 22 | Nogle gange (5–29 %) | I 2 tilstande |
| PODXLpodocalyxin like | Nogle gange (5–29 %) | I 1 tilstand |
| PRKNparkin RBR E3 ubiquitin protein ligase | Nogle gange (5–29 %) | I 1 tilstand |
| PUS3pseudouridine synthase 3 | Nogle gange (5–29 %) | I 1 tilstand |
| RNASEH1ribonuclease H1 | Nogle gange (5–29 %) | I 1 tilstand |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Nogle gange (5–29 %) | I 1 tilstand |
| SLC52A3solute carrier family 52 member 3 | Nogle gange (5–29 %) | I 1 tilstand |
| SNCAsynuclein alpha | Nogle gange (5–29 %) | I 1 tilstand |
| SYNJ1synaptojanin 1 | Nogle gange (5–29 %) | I 1 tilstand |
| UBE3Aubiquitin protein ligase E3A | Nogle gange (5–29 %) | I 3 tilstande |
| UCHL1ubiquitin C-terminal hydrolase L1 | Nogle gange (5–29 %) | I 1 tilstand |
| USH2Ausherin | Nogle gange (5–29 %) | I 1 tilstand |
| VPS13Cvacuolar protein sorting 13 homolog C | Nogle gange (5–29 %) | I 1 tilstand |
| WHRNwhirlin | Nogle gange (5–29 %) | I 1 tilstand |
| ARL6ARF like GTPase 6 | Ikke registreret | I 1 tilstand |
| BBS1Bardet-Biedl syndrome 1 | Ikke registreret | I 1 tilstand |
| CCDC28Bcoiled-coil domain containing 28B | Ikke registreret | I 1 tilstand |
Hvor hyppigt det ses hos personer med en af genets tilstande, den hyppigste værdi på tværs af dem, sådan som Human Phenotype Ontology registrerer det. Disse sider beskriver egenskaber og den forskning, der ligger bag dem. De er ikke en diagnose, og hvis du har spørgsmål om symptomer, bør du spørge en læge eller genetisk rådgiver.
Bredere træk
Hvor oplysningerne kommer fra
- Human Phenotype Ontology, udgivelse 2026-09-01: egenskaben, dens navne, definition og de gener, der er knyttet til den. Læs mere på hpo.jax.org.
- Dataudgivelse 2026.10.21-777c9289.
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