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Merkmal
Involuntary movements
Involuntary contractions of muscle leading to involuntary movements of extremities, neck, trunk, or face.
Zusammenfassung
- Auch genannt
- Involuntary muscle contractions
- Körpersystem
- Abnormality of the nervous system
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Diese Seite als Daten
Hängen Sie .json an die Adresse der Seite an oder fordern Sie application/json an, um sie als JSON zu lesen.
library(jsonlite)
url <- "https://dantelabs.com/traits/involuntary-movements.json"
page <- fromJSON(url)
page$trait$nameInvoluntary movementsHP:0004305
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Lesen Sie die Gene aus, die mit Involuntary movements zusammenhängen, und den Rest Ihres Genoms, mit einem einzigen Test.
Ab 449 $Kostenloser Versand · Ergebnisse in 6–8 Wochen
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.
- Epilepsy (Full Panel)Reads 63 of these genesSYNJ1CDKL5GABBR2KCNA1MECP2PRRT2About this report →
- Basal Ganglia CalcificationReads 7 of these genesJAM2MYORGNAA60PDGFBPDGFRBSLC20A2About this report →
- Familial Hemiplegic MigraineReads 3 of these genesATP1A2CACNA1ASCN1AAbout this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 10 of these genesKCNJ10PRRT2HPCAPNKDSLC2A1TMEM151AAbout this report →
Show 52 more reports
- Hereditary Episodic AtaxiasReads 3 of these genesKCNA1CACNA1ASCN2AAbout this report →
- Neuroacanthocytosis and Huntington Disease PhenocopiesReads 2 of these genesVPS13AJPH3About this report →
- ADCY5-Related DyskinesiaReads 1 of these genesADCY5About this report →
- ATP1A2-Related Fetal Akinesia with PolymicrogyriaReads 1 of these genesATP1A2About this report →
- DHX30-Related Neurodevelopmental DisorderReads 1 of these genesDHX30About this report →
- Dravet SyndromeReads 1 of these genesSCN1AAbout this report →
- Genetic Prion Disease (incl. Fatal Familial Insomnia)Reads 1 of these genesPRNPAbout this report →
- HPCA-Related DystoniaReads 1 of these genesHPCAAbout this report →
- Huntington DiseaseReads 1 of these genesHTTAbout this report →
- KCNQ2-Related Neonatal Encephalopathy with Non-Epileptic MyoclonusReads 1 of these genesKCNQ2About this report →
- NGLY1 DeficiencyReads 1 of these genesNGLY1About this report →
- Rett Syndrome and MECP2-Related DisordersReads 1 of these genesMECP2About this report →
- Inherited Neurodegenerative DisordersReads 16 of these genesTWNKVPS13AATN1CACNA1ACPFTLAbout this report →
- Intellectual DisabilityReads 12 of these genesDEAF1MECP2GRIK2GRIN1SCN2ACAMK2AAbout this report →
- Parkinson DiseaseReads 3 of these genesSYNJ1DNAJC6MAPTAbout this report →
- Fibrodysplasia Ossificans ProgressivaReads 1 of these genesGNASAbout this report →
- Hereditary FibromatosesReads 1 of these genesPDGFRBAbout this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 4 of these genesATN1CACNA1ATBPATP1A3About this report →
- Complex Neurodevelopmental Disorder With Motor FeaturesReads 2 of these genesCACNA1ACACNA1BAbout this report →
- Neurodegeneration with Brain Iron Accumulation (NBIA)Reads 2 of these genesCPFTLAbout this report →
- Primary Mitochondrial DiseaseReads 6 of these genesTWNKDNAJC30AIFM1CARS2GFM2LIG3About this report →
- Cutis LaxaReads 2 of these genesELNATP6V1AAbout this report →
- Inherited Iron Metabolism DisordersReads 1 of these genesCPAbout this report →
- Pseudohypoparathyroidism & GNAS-Inactivation DisordersReads 1 of these genesGNASAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 7 of these genesVPS13AAIFM1IARS2AARS1GFM2LIG3About this report →
- Pontocerebellar Hypoplasia (TSEN54 and MINPP1)Reads 2 of these genesCHMP1ATOE1About this report →
- Lissencephaly Spectrum DisordersReads 2 of these genesCEP85LMACF1About this report →
- Chronic Granulomatous DiseaseReads 1 of these genesNCF1About this report →
- Cornelia de Lange SyndromeReads 1 of these genesSMC1AAbout this report →
- Leigh SyndromeReads 3 of these genesAIFM1GFM2MECRAbout this report →
- Congenital Disorders of GlycosylationReads 3 of these genesPGAP3DHDDSNUS1About this report →
- Familial HypomagnesemiaReads 1 of these genesKCNJ10About this report →
- Frontotemporal DementiaReads 1 of these genesMAPTAbout this report →
- Hereditary Optic NeuropathyReads 1 of these genesATP1A3About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesELNAbout this report →
- Congenital Stationary Night BlindnessReads 1 of these genesCABP4About this report →
- Charcot-Marie-Tooth DiseaseReads 2 of these genesAIFM1AARS1About this report →
- Other Inherited LeukodystrophiesReads 2 of these genesAARS1TUBB4AAbout this report →
- Congenital HypothyroidismReads 1 of these genesNKX2-1About this report →
- GPI Anchor Biosynthesis DefectsReads 1 of these genesPGAP3About this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 1 of these genesAIFM1About this report →
- Hereditary Congenital & Juvenile CataractReads 1 of these genesFTLAbout this report →
- Syndromic Complex Neurodevelopmental DisorderReads 1 of these genesZFXAbout this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 1 of these genesTUBB4AAbout this report →
- Nephrotic SyndromeReads 1 of these genesPODXLAbout this report →
- Thyroid CancerReads 1 of these genesGNASAbout this report →
- Male InfertilityReads 1 of these genesFKBP6About this report →
- Female InfertilityReads 1 of these genesTWNKAbout this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesTWNKAbout this report →
- Retinitis PigmentosaReads 1 of these genesDHDDSAbout this report →
- Hearing Loss and DeafnessReads 1 of these genesAIFM1About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesNCF1About this report →
Lesen Sie die Gene aus, die mit Involuntary movements zusammenhängen, und den Rest Ihres Genoms, mit einem einzigen Test.
Ab 449 $Kostenloser Versand · Ergebnisse in 6–8 Wochen
Meinen Genome Test bestellen143 Gene mit Involuntary movements verknüpft
Veränderungen in diesen Genen verursachen seltene Erkrankungen, bei denen Involuntary movements 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 |
|---|---|---|
| DEAF1DEAF1 transcription factor | Immer | In 2 Erkrankungen |
| MDGA2MAM domain containing glycosylphosphatidylinositol anchor 2 | Immer | In 2 Erkrankungen |
| SYNJ1synaptojanin 1 | Immer | In 3 Erkrankungen |
| TWNKtwinkle mtDNA helicase | Immer | In 1 Erkrankung |
| BAZ1Bbromodomain adjacent to zinc finger domain 1B | Sehr häufig (80–99 %) | In 1 Erkrankung |
| BUD23BUD23 rRNA methyltransferase and ribosome maturation factor | Sehr häufig (80–99 %) | In 1 Erkrankung |
| CDKL5cyclin dependent kinase like 5 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| CLIP2CAP-Gly domain containing linker protein 2 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| DNAJC30DnaJ heat shock protein family (Hsp40) member C30 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| EIF4Heukaryotic translation initiation factor 4H | Sehr häufig (80–99 %) | In 1 Erkrankung |
| ELNelastin | Sehr häufig (80–99 %) | In 1 Erkrankung |
| FKBP6FKBP prolyl isomerase family member 6 (inactive) | Sehr häufig (80–99 %) | In 1 Erkrankung |
| GABBR2gamma-aminobutyric acid type B receptor subunit 2 | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| GTF2Igeneral transcription factor IIi | Sehr häufig (80–99 %) | In 1 Erkrankung |
| GTF2IRD1GTF2I repeat domain containing 1 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| GTF2IRD2GTF2I repeat domain containing 2 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| KCNA1potassium voltage-gated channel subfamily A member 1 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| KCNJ10potassium inwardly rectifying channel subfamily J member 10 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| LIMK1LIM domain kinase 1 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| MECP2methyl-CpG binding protein 2 | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| METTL27methyltransferase like 27 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| NCF1neutrophil cytosolic factor 1 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| NGLY1N-glycanase 1 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| NTNG1netrin G1 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| PRRT2proline rich transmembrane protein 2 | Sehr häufig (80–99 %) | In 5 Erkrankungen |
| RFC2replication factor C subunit 2 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| SMC1Astructural maintenance of chromosomes 1A | Sehr häufig (80–99 %) | In 1 Erkrankung |
| STX1Asyntaxin 1A | Sehr häufig (80–99 %) | In 1 Erkrankung |
| TBL2transducin beta like 2 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| TMEM270transmembrane protein 270 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| VPS13Avacuolar protein sorting 13 homolog A | Sehr häufig (80–99 %) | In 1 Erkrankung |
| VPS37DVPS37D subunit of ESCRT-I | Sehr häufig (80–99 %) | In 1 Erkrankung |
| ADCY5adenylate cyclase 5 | Häufig (30–79 %) | In 1 Erkrankung |
| AIFM1apoptosis inducing factor mitochondria associated 1 | Häufig (30–79 %) | In 2 Erkrankungen |
| ATN1atrophin 1 | Häufig (30–79 %) | In 1 Erkrankung |
| ATP1A2ATPase Na+/K+ transporting subunit alpha 2 | Häufig (30–79 %) | In 2 Erkrankungen |
| CABP4calcium binding protein 4 | Häufig (30–79 %) | In 1 Erkrankung |
| CACNA1Acalcium voltage-gated channel subunit alpha1 A | Häufig (30–79 %) | In 2 Erkrankungen |
| CEP85Lcentrosomal protein 85L | Häufig (30–79 %) | In 1 Erkrankung |
| CHRNA2cholinergic receptor nicotinic alpha 2 subunit | Häufig (30–79 %) | In 1 Erkrankung |
103 weitere Gene anzeigen
| Gen | Wie häufig es auftritt | Erkrankungen |
|---|---|---|
| CHRNA4cholinergic receptor nicotinic alpha 4 subunit | Häufig (30–79 %) | In 1 Erkrankung |
| CHRNB2cholinergic receptor nicotinic beta 2 subunit | Häufig (30–79 %) | In 1 Erkrankung |
| CPceruloplasmin | Häufig (30–79 %) | In 1 Erkrankung |
| CRHcorticotropin releasing hormone | Häufig (30–79 %) | In 1 Erkrankung |
| DEPDC5DEP domain containing 5, GATOR1 subcomplex subunit | Häufig (30–79 %) | In 2 Erkrankungen |
| DNAJC6DnaJ heat shock protein family (Hsp40) member C6 | Häufig (30–79 %) | In 1 Erkrankung |
| DNM1dynamin 1 | Häufig (30–79 %) | In 2 Erkrankungen |
| FTLferritin light chain | Häufig (30–79 %) | In 1 Erkrankung |
| GRIK2glutamate ionotropic receptor kainate type subunit 2 | Häufig (30–79 %) | In 1 Erkrankung |
| GRIN1glutamate ionotropic receptor NMDA type subunit 1 | Häufig (30–79 %) | In 1 Erkrankung |
| HPCAhippocalcin | Häufig (30–79 %) | In 1 Erkrankung |
| HTThuntingtin | Häufig (30–79 %) | In 1 Erkrankung |
| IARS2isoleucyl-tRNA synthetase 2, mitochondrial | Häufig (30–79 %) | In 1 Erkrankung |
| KCNQ2potassium voltage-gated channel subfamily Q member 2 | Häufig (30–79 %) | In 1 Erkrankung |
| KCNQ3potassium voltage-gated channel subfamily Q member 3 | Häufig (30–79 %) | In 1 Erkrankung |
| KCNT1potassium sodium-activated channel subfamily T member 1 | Häufig (30–79 %) | In 1 Erkrankung |
| MACF1microtubule actin crosslinking factor 1 | Häufig (30–79 %) | In 2 Erkrankungen |
| MAPTmicrotubule associated protein tau | Häufig (30–79 %) | In 1 Erkrankung |
| MICU1mitochondrial calcium uptake 1 | Häufig (30–79 %) | In 1 Erkrankung |
| PGAP3post-GPI attachment to proteins phospholipase 3 | Häufig (30–79 %) | In 1 Erkrankung |
| PNKDPNKD metallo-beta-lactamase domain containing | Häufig (30–79 %) | In 1 Erkrankung |
| PODXLpodocalyxin like | Häufig (30–79 %) | In 1 Erkrankung |
| PRNPprion protein (Kanno blood group) | Häufig (30–79 %) | In 1 Erkrankung |
| SCN1Asodium voltage-gated channel alpha subunit 1 | Häufig (30–79 %) | In 2 Erkrankungen |
| SCN2Asodium voltage-gated channel alpha subunit 2 | Häufig (30–79 %) | In 1 Erkrankung |
| SCN8Asodium voltage-gated channel alpha subunit 8 | Häufig (30–79 %) | In 2 Erkrankungen |
| SLC2A1solute carrier family 2 member 1 | Häufig (30–79 %) | In 1 Erkrankung |
| SLC2A3solute carrier family 2 member 3 | Häufig (30–79 %) | In 1 Erkrankung |
| TANGO2transport and golgi organization 2 homolog | Häufig (30–79 %) | In 1 Erkrankung |
| TBPTATA-box binding protein | Häufig (30–79 %) | In 1 Erkrankung |
| TMEM151Atransmembrane protein 151A | Häufig (30–79 %) | In 1 Erkrankung |
| AARS1alanyl-tRNA synthetase 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| ACTL6Bactin like 6B | Manchmal (5–29 %) | In 1 Erkrankung |
| AP3B2adaptor related protein complex 3 subunit beta 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| ATP1A3ATPase Na+/K+ transporting subunit alpha 3 | Manchmal (5–29 %) | In 1 Erkrankung |
| ATP6V1AATPase H+ transporting V1 subunit A | Manchmal (5–29 %) | In 1 Erkrankung |
| CACNA1Bcalcium voltage-gated channel subunit alpha1 B | Manchmal (5–29 %) | In 1 Erkrankung |
| CACNA2D1calcium voltage-gated channel auxiliary subunit alpha2delta 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| CAMK2Acalcium/calmodulin dependent protein kinase II alpha | Manchmal (5–29 %) | In 1 Erkrankung |
| CARS2cysteinyl-tRNA synthetase 2, mitochondrial | Manchmal (5–29 %) | In 1 Erkrankung |
| CDK19cyclin dependent kinase 19 | Manchmal (5–29 %) | In 1 Erkrankung |
| CELF2CUGBP Elav-like family member 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| CHMP1Acharged multivesicular body protein 1A | Manchmal (5–29 %) | In 1 Erkrankung |
| CLTCclathrin heavy chain | Manchmal (5–29 %) | In 1 Erkrankung |
| CMPK2cytidine/uridine monophosphate kinase 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| CNKSR2connector enhancer of kinase suppressor of Ras 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| CYFIP2cytoplasmic FMR1 interacting protein 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| DALRD3DALR anticodon binding domain containing 3 | Manchmal (5–29 %) | In 1 Erkrankung |
| DHDDSdehydrodolichyl diphosphate synthase subunit | Manchmal (5–29 %) | In 1 Erkrankung |
| EEF1A2eukaryotic translation elongation factor 1 alpha 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| FBXO28F-box protein 28 | Manchmal (5–29 %) | In 1 Erkrankung |
| FGF12fibroblast growth factor 12 | Manchmal (5–29 %) | In 1 Erkrankung |
| FOXG1forkhead box G1 | Manchmal (5–29 %) | In 1 Erkrankung |
| FZR1fizzy and cell division cycle 20 related 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| GABRA2gamma-aminobutyric acid type A receptor subunit alpha2 | Manchmal (5–29 %) | In 1 Erkrankung |
| GABRA5gamma-aminobutyric acid type A receptor subunit alpha5 | Manchmal (5–29 %) | In 1 Erkrankung |
| GABRB2gamma-aminobutyric acid type A receptor subunit beta2 | Manchmal (5–29 %) | In 1 Erkrankung |
| GABRG2gamma-aminobutyric acid type A receptor subunit gamma2 | Manchmal (5–29 %) | In 1 Erkrankung |
| GFM2GTP dependent ribosome recycling factor mitochondrial 2 | Manchmal (5–29 %) | In 2 Erkrankungen |
| GNASGNAS complex locus | Manchmal (5–29 %) | In 1 Erkrankung |
| GRIN2Dglutamate ionotropic receptor NMDA type subunit 2D | Manchmal (5–29 %) | In 1 Erkrankung |
| HCN1hyperpolarization activated cyclic nucleotide gated potassium channel 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| JAM2junctional adhesion molecule 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| JPH3junctophilin 3 | Manchmal (5–29 %) | In 1 Erkrankung |
| KCNA2potassium voltage-gated channel subfamily A member 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| KCNB1potassium voltage-gated channel subfamily B member 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| KCNC2potassium voltage-gated channel subfamily C member 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| KCNH5potassium voltage-gated channel subfamily H member 5 | Manchmal (5–29 %) | In 1 Erkrankung |
| LIG3DNA ligase 3 | Manchmal (5–29 %) | In 1 Erkrankung |
| MYORGmyogenesis regulating glycosidase | Manchmal (5–29 %) | In 1 Erkrankung |
| NAA60N-alpha-acetyltransferase 60, NatF catalytic subunit | Manchmal (5–29 %) | In 1 Erkrankung |
| NECAP1NECAP endocytosis associated 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| NKX2-1NK2 homeobox 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| NTRK2neurotrophic receptor tyrosine kinase 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| NUS1NUS1 dehydrodolichyl diphosphate synthase subunit | Manchmal (5–29 %) | In 1 Erkrankung |
| PACS2phosphofurin acidic cluster sorting protein 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| PARS2prolyl-tRNA synthetase 2, mitochondrial | Manchmal (5–29 %) | In 1 Erkrankung |
| PDGFBplatelet derived growth factor subunit B | Manchmal (5–29 %) | In 1 Erkrankung |
| PDGFRBplatelet derived growth factor receptor beta | Manchmal (5–29 %) | In 1 Erkrankung |
| PPP3CAprotein phosphatase 3 catalytic subunit alpha | Manchmal (5–29 %) | In 1 Erkrankung |
| RRP12ribosomal RNA processing 12 homolog | Manchmal (5–29 %) | In 1 Erkrankung |
| SCN3Asodium voltage-gated channel alpha subunit 3 | Manchmal (5–29 %) | In 1 Erkrankung |
| SLC13A5solute carrier family 13 member 5 | Manchmal (5–29 %) | In 2 Erkrankungen |
| SLC1A2solute carrier family 1 member 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| SLC20A2solute carrier family 20 member 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| SLC38A3solute carrier family 38 member 3 | Manchmal (5–29 %) | In 1 Erkrankung |
| SMSspermine synthase | Manchmal (5–29 %) | In 1 Erkrankung |
| SYNGAP1synaptic Ras GTPase activating protein 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| SZT2SZT2 subunit of KICSTOR complex | Manchmal (5–29 %) | In 1 Erkrankung |
| TOE1target of EGR1, exonuclease | Manchmal (5–29 %) | In 1 Erkrankung |
| TRAK1trafficking kinesin protein 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| TUBB4Atubulin beta 4A class IVa | Manchmal (5–29 %) | In 1 Erkrankung |
| UBA5ubiquitin like modifier activating enzyme 5 | Manchmal (5–29 %) | In 1 Erkrankung |
| UFSP2UFM1 specific peptidase 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| XPR1xenotropic and polytropic retrovirus receptor 1 | Manchmal (5–29 %) | In 2 Erkrankungen |
| YWHAGtyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein gamma | Manchmal (5–29 %) | In 1 Erkrankung |
| ZFXzinc finger protein X-linked | Manchmal (5–29 %) | In 1 Erkrankung |
| DHX30DExH-box helicase 30 | Nicht erfasst | In 1 Erkrankung |
| GNAO1G protein subunit alpha o1 | Nicht erfasst | In 1 Erkrankung |
| GPR88G protein-coupled receptor 88 | Nicht erfasst | In 1 Erkrankung |
| MECRmitochondrial trans-2-enoyl-CoA reductase | Nicht erfasst | In 1 Erkrankung |
| PRKRAprotein activator of interferon induced protein kinase EIF2AK2 | Nicht erfasst | In 1 Erkrankung |
| SYT1synaptotagmin 1 | 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.
Untergeordnete Merkmale
- Tremor495 Gene
- Jerking352 Gene
- Chorea189 Gene
- Clonus98 Gene
- Muscle twitch91 Gene
- Involuntary writhing movements in fingers, hands, toes, and feet69 Gene
- Paroxysmal dyskinesia22 Gene
- Alien limb phenomenon4 Gene
- Hemiballismus4 Gene
- Akathisia1 Gen
- Chvostek sign1 Gen
- Self-mutilation of tongue and lips due to involuntary movements1 Gen
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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