Tratto
Intention tremor
A type of kinetic tremor that occurs during target directed movement is called intention tremor. That is, an oscillatory cerebellar ataxia that tends to be absent when the limbs are inactive and during the first part of voluntary movement but worsening as the movement continues and greater precision is required (e.g., in touching a target such as the patient's nose or a physician's finger).
Riepilogo
- Sistema corporeo
- Abnormality of the nervous system
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page$trait$nameLeggi i geni collegati a Intention tremor e il resto del tuo genoma con un unico test.
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Ottieni il mio Genome Test62 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.
- Inherited Neurodegenerative DisordersReads 49 of these genesABCB7ATP2B3CWF19L1FMR1ITPR1PLP1About this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 11 of these genesITPR1SPTBN2CACNA1AATXN10TGM6TMEM240About this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 9 of these genesPLP1HYCC1POLR3BEPRS1POLR3ARARS1About this report →
- Other Inherited LeukodystrophiesReads 15 of these genesPLP1PSAPSCP2HYCC1POLR3BEPRS1About this report →
Show 58 more reports
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 11 of these genesCWF19L1SPTBN2ATCAYFXNRFC1SCYL1About this report →
- Metachromatic LeukodystrophyReads 2 of these genesPSAPARSAAbout this report →
- Ataxia-TelangiectasiaReads 1 of these genesATMAbout this report →
- Fragile X SyndromeReads 1 of these genesFMR1About this report →
- Friedreich AtaxiaReads 1 of these genesFXNAbout this report →
- Glutathione Synthetase DeficiencyReads 1 of these genesGSSAbout this report →
- PNPLA6-Related Ataxia, Retinal Dystrophy and HypogonadismReads 1 of these genesPNPLA6About this report →
- POLR3A-Related DisorderReads 1 of these genesPOLR3AAbout this report →
- POLR3B-Related DisorderReads 1 of these genesPOLR3BAbout this report →
- Primary Microcephaly 26 (LMNB1)Reads 1 of these genesLMNB1About this report →
- SPTBN1-Related Neurodevelopmental DisorderReads 1 of these genesSPTBN1About this report →
- UNC13A-Related Neurodevelopmental DisordersReads 1 of these genesUNC13AAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 14 of these genesPOLGPSAPPOLR3BFARS2GJB1RFC1About this report →
- DNA Repair DiseaseReads 6 of these genesERCC6ERCC8MRE11ERCC2ERCC3GTF2H5About this report →
- Peroxisomal Enzyme Disorders & Refsum DiseaseReads 2 of these genesAMACRHSD17B4About this report →
- Parkinson DiseaseReads 3 of these genesFBXO7SNCAPLA2G6About this report →
- Hereditary Spastic ParaplegiaReads 6 of these genesPLP1PNPLA6UCHL1FARS2KIF1CGJC2About this report →
- Activated PI3K-Delta Syndrome (APDS)Reads 1 of these genesPIK3CDAbout this report →
- Cowden Syndrome (PTEN hamartoma tumour syndrome)Reads 1 of these genesPTENAbout this report →
- Hereditary AmyloidosisReads 2 of these genesTTRITM2BAbout this report →
- Cerebral Amyloid AngiopathyReads 1 of these genesITM2BAbout this report →
- Familial Hemiplegic MigraineReads 1 of these genesCACNA1AAbout this report →
- Stargardt DiseaseReads 1 of these genesELOVL4About this report →
- Adult-Onset Leukodystrophies (CSF1R, LMNB1, Nasu-Hakola)Reads 1 of these genesLMNB1About this report →
- Hereditary Episodic AtaxiasReads 1 of these genesCACNA1AAbout this report →
- Thiamine Transporter and Metabolism DisordersReads 1 of these genesTPK1About this report →
- MTOR Pathway Megalencephaly and Overgrowth DisordersReads 1 of these genesPIK3CAAbout this report →
- Epilepsy (Full Panel)Reads 6 of these genesSEMA6BCACNA1ACSTBPRICKLE1SCARB2AARS1About this report →
- Female InfertilityReads 3 of these genesFMR1ATMHSD17B4About this report →
- Hepatic Porphyria DisordersReads 1 of these genesHMBSAbout this report →
- Hereditary Sideroblastic AnaemiasReads 1 of these genesABCB7About this report →
- Charcot-Marie-Tooth DiseaseReads 3 of these genesPOLR3BGJB1AARS1About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 2 of these genesTSPOAP1KCNJ10About this report →
- Anterior Segment Dysgenesis, Axenfeld-Rieger Syndrome & AniridiaReads 1 of these genesITPR1About this report →
- Breast and Ovarian Cancer Genes Beyond BRCA1/2Reads 1 of these genesATMAbout this report →
- Complex Neurodevelopmental Disorder With Motor FeaturesReads 1 of these genesCACNA1AAbout this report →
- PorphyriaReads 1 of these genesHMBSAbout this report →
- Intellectual DisabilityReads 5 of these genesKDM6BSEMA6BQRICH1NONOOPHN1About this report →
- Long QT SyndromeReads 1 of these genesCACNA1CAbout this report →
- Neurodegeneration with Brain Iron Accumulation (NBIA)Reads 1 of these genesPLA2G6About this report →
- Familial HypomagnesemiaReads 1 of these genesKCNJ10About this report →
- HyperinsulinismReads 1 of these genesPMM2About this report →
- Zellweger Spectrum & Peroxisome Biogenesis DisordersReads 1 of these genesPEX10About this report →
- Lysosomal Storage DiseaseReads 2 of these genesPSAPARSAAbout this report →
- Primary Mitochondrial DiseaseReads 3 of these genesPOLGFARS2TMEM70About this report →
- Primary Lymphoedema & Lymphatic MalformationsReads 1 of these genesGJC2About this report →
- Leigh SyndromeReads 2 of these genesFARS2TPK1About this report →
- Congenital HypothyroidismReads 1 of these genesNKX2-1About this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 1 of these genesRFC1About this report →
- Pontocerebellar Hypoplasia (TSEN54 and MINPP1)Reads 1 of these genesSLC25A46About this report →
- Hereditary Congenital & Juvenile CataractReads 1 of these genesLEMD2About this report →
- Lissencephaly Spectrum DisordersReads 1 of these genesLAMB1About this report →
- Syndromic Complex Neurodevelopmental DisorderReads 1 of these genesQRICH1About this report →
- Syndromic CraniosynostosisReads 1 of these genesRNU12About this report →
- Microphthalmia, Anophthalmia & ColobomaReads 1 of these genesERCC2About this report →
- Osteogenesis ImperfectaReads 1 of these genesPOLR3AAbout this report →
- Other Inborn Errors of ImmunityReads 2 of these genesATMPIK3CDAbout this report →
- Congenital Disorders of GlycosylationReads 1 of these genesPMM2About this report →
Leggi i geni collegati a Intention tremor e il resto del tuo genoma con un unico test.
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Ottieni il mio Genome Test115 geni collegati a Intention tremor
Alterazioni in questi geni causano malattie rare in cui si osserva Intention tremor. La maggior parte delle persone con questo tratto non presenta nessuna di tali condizioni, e un gene di questo elenco non dice nulla sul genoma di nessuno in particolare.
| Gene | Frequenza di osservazione | Condizioni |
|---|---|---|
| ABCB7ATP binding cassette subfamily B member 7 | Sempre | In 1 condizione |
| AMACRalpha-methylacyl-CoA racemase | Sempre | In 1 condizione |
| ATP2B3ATPase plasma membrane Ca2+ transporting 3 | Sempre | In 2 condizioni |
| CWF19L1CWF19 like cell cycle control factor 1 | Sempre | In 2 condizioni |
| FMR1fragile X messenger ribonucleoprotein 1 | Sempre | In 2 condizioni |
| INPP4Ainositol polyphosphate-4-phosphatase type I A | Sempre | In 1 condizione |
| ITPR1inositol 1,4,5-trisphosphate receptor type 1 | Sempre | In 3 condizioni |
| KDM6Blysine demethylase 6B | Sempre | In 1 condizione |
| LAMB1laminin subunit beta 1 | Sempre | In 1 condizione |
| LEMD2LEM domain nuclear envelope protein 2 | Sempre | In 1 condizione |
| LMAN2Llectin, mannose binding 2 like | Sempre | In 1 condizione |
| MALmal, T cell differentiation protein (MAL blood group) | Sempre | In 1 condizione |
| PLP1proteolipid protein 1 | Sempre | In 1 condizione |
| PNPLA6patatin like domain 6, lysophospholipase | Sempre | In 2 condizioni |
| POLGDNA polymerase gamma, catalytic subunit | Sempre | In 1 condizione |
| POU4F1POU class 4 homeobox 1 | Sempre | In 2 condizioni |
| PPP2R5Cprotein phosphatase 2 regulatory subunit B'gamma | Sempre | In 1 condizione |
| PSAPprosaposin | Sempre | In 3 condizioni |
| RNU12RNA, U12 small nuclear | Sempre | In 2 condizioni |
| SCP2sterol carrier protein 2 | Sempre | In 1 condizione |
| SEMA6Bsemaphorin 6B | Sempre | In 1 condizione |
| SMG9SMG9 nonsense mediated mRNA decay factor | Sempre | In 1 condizione |
| SPTBN2spectrin beta, non-erythrocytic 2 | Sempre | In 3 condizioni |
| TENM4teneurin transmembrane protein 4 | Sempre | In 1 condizione |
| UCHL1ubiquitin C-terminal hydrolase L1 | Sempre | In 2 condizioni |
| UNC13Aunc-13 homolog A | Sempre | In 1 condizione |
| CACNA1Acalcium voltage-gated channel subunit alpha1 A | Molto spesso (80–99%) | In 2 condizioni |
| HYCC1hyccin PI4KA lipid kinase complex subunit 1 | Molto spesso (80–99%) | In 1 condizione |
| POLR3BRNA polymerase III subunit B | Molto spesso (80–99%) | In 1 condizione |
| ATCAYATCAY kinesin light chain interacting caytaxin | Spesso (30–79%) | In 2 condizioni |
| ATMATM serine/threonine kinase | Spesso (30–79%) | In 1 condizione |
| ATXN10ataxin 10 | Spesso (30–79%) | In 1 condizione |
| CCDC88Ccoiled-coil and HOOK domain protein 88C | Spesso (30–79%) | In 2 condizioni |
| CSTBcystatin B | Spesso (30–79%) | In 1 condizione |
| EPRS1glutamyl-prolyl-tRNA synthetase 1 | Spesso (30–79%) | In 1 condizione |
| ERCC6ERCC excision repair 6, chromatin remodeling factor | Spesso (30–79%) | In 1 condizione |
| ERCC8ERCC excision repair 8, CSA ubiquitin ligase complex subunit | Spesso (30–79%) | In 1 condizione |
| FARS2phenylalanyl-tRNA synthetase 2, mitochondrial | Spesso (30–79%) | In 1 condizione |
| FBXO7F-box protein 7 | Spesso (30–79%) | In 1 condizione |
| FXNfrataxin | Spesso (30–79%) | In 1 condizione |
Mostra altri 75 geni
| Gene | Frequenza di osservazione | Condizioni |
|---|---|---|
| GJB1gap junction protein beta 1 | Spesso (30–79%) | In 1 condizione |
| HMBShydroxymethylbilane synthase | Spesso (30–79%) | In 1 condizione |
| HSD17B4hydroxysteroid 17-beta dehydrogenase 4 | Spesso (30–79%) | In 1 condizione |
| KCNK4potassium two pore domain channel subfamily K member 4 | Spesso (30–79%) | In 1 condizione |
| KCNN2potassium calcium-activated channel subfamily N member 2 | Spesso (30–79%) | In 1 condizione |
| KNSTRNkinetochore localized astrin (SPAG5) binding protein | Spesso (30–79%) | In 1 condizione |
| MRE11MRE11 double strand break repair nuclease | Spesso (30–79%) | In 1 condizione |
| PI4KAphosphatidylinositol 4-kinase alpha | Spesso (30–79%) | In 1 condizione |
| PIK3CDphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | Spesso (30–79%) | In 1 condizione |
| PMM2phosphomannomutase 2 | Spesso (30–79%) | In 1 condizione |
| POLR3ARNA polymerase III subunit A | Spesso (30–79%) | In 2 condizioni |
| PRICKLE1prickle planar cell polarity protein 1 | Spesso (30–79%) | In 1 condizione |
| QRICH1glutamine rich 1 | Spesso (30–79%) | In 1 condizione |
| RAB3ARAB3A, member RAS oncogene family | Spesso (30–79%) | In 1 condizione |
| RARS1arginyl-tRNA synthetase 1 | Spesso (30–79%) | In 2 condizioni |
| RBSNrabenosyn, RAB effector | Spesso (30–79%) | In 1 condizione |
| RFC1replication factor C subunit 1 | Spesso (30–79%) | In 1 condizione |
| SCARB2scavenger receptor class B member 2 | Spesso (30–79%) | In 2 condizioni |
| SCYL1SCY1 like pseudokinase 1 | Spesso (30–79%) | In 1 condizione |
| SNCAsynuclein alpha | Spesso (30–79%) | In 1 condizione |
| TECRtrans-2,3-enoyl-CoA reductase | Spesso (30–79%) | In 1 condizione |
| TGM6transglutaminase 6 | Spesso (30–79%) | In 2 condizioni |
| TMCO1transmembrane and coiled-coil domains 1 | Spesso (30–79%) | In 1 condizione |
| TMEM106Btransmembrane protein 106B | Spesso (30–79%) | In 1 condizione |
| TMEM240transmembrane protein 240 | Spesso (30–79%) | In 1 condizione |
| TPRtranslocated promoter region, nuclear basket protein | Spesso (30–79%) | In 1 condizione |
| TSPOAP1TSPO associated protein 1 | Spesso (30–79%) | In 1 condizione |
| WDR81WD repeat domain 81 | Spesso (30–79%) | In 1 condizione |
| AARS1alanyl-tRNA synthetase 1 | A volte (5–29%) | In 1 condizione |
| ABHD12abhydrolase domain containing 12, lysophospholipase | A volte (5–29%) | In 1 condizione |
| ADPRSADP-ribosylserine hydrolase | A volte (5–29%) | In 1 condizione |
| ANO10anoctamin 10 | A volte (5–29%) | In 2 condizioni |
| ARSAarylsulfatase A | A volte (5–29%) | In 2 condizioni |
| CACNA1Ccalcium voltage-gated channel subunit alpha1 C | A volte (5–29%) | In 1 condizione |
| CARS1cysteinyl-tRNA synthetase 1 | A volte (5–29%) | In 1 condizione |
| CTDP1CTD phosphatase 1 | A volte (5–29%) | In 1 condizione |
| DBR1debranching RNA lariats 1 | A volte (5–29%) | In 1 condizione |
| EEFSECeukaryotic elongation factor, selenocysteine-tRNA specific | A volte (5–29%) | In 1 condizione |
| ELOVL4ELOVL fatty acid elongase 4 | A volte (5–29%) | In 1 condizione |
| ERCC2ERCC excision repair 2, TFIIH core complex helicase subunit | A volte (5–29%) | In 1 condizione |
| ERCC3ERCC excision repair 3, TFIIH core complex helicase subunit | A volte (5–29%) | In 1 condizione |
| GTF2E2general transcription factor IIE subunit 2 | A volte (5–29%) | In 1 condizione |
| GTF2H5general transcription factor IIH subunit 5 | A volte (5–29%) | In 1 condizione |
| KIF1Ckinesin family member 1C | A volte (5–29%) | In 1 condizione |
| LMNB1lamin B1 | A volte (5–29%) | In 1 condizione |
| MPLKIPM-phase specific PLK1 interacting protein | A volte (5–29%) | In 1 condizione |
| NKX2-1NK2 homeobox 1 | A volte (5–29%) | In 1 condizione |
| NONOnon-POU domain containing octamer binding | A volte (5–29%) | In 1 condizione |
| OPHN1oligophrenin 1 | A volte (5–29%) | In 1 condizione |
| PEX10peroxisomal biogenesis factor 10 | A volte (5–29%) | In 1 condizione |
| PPP2R2Bprotein phosphatase 2 regulatory subunit Bbeta | A volte (5–29%) | In 1 condizione |
| RFC4replication factor C subunit 4 | A volte (5–29%) | In 1 condizione |
| RNF113Aring finger protein 113A | A volte (5–29%) | In 1 condizione |
| SACSsacsin molecular chaperone | A volte (5–29%) | In 1 condizione |
| SLC25A46solute carrier family 25 member 46 | A volte (5–29%) | In 1 condizione |
| TARS1threonyl-tRNA synthetase 1 | A volte (5–29%) | In 1 condizione |
| TMEM63Atransmembrane protein 63A | A volte (5–29%) | In 1 condizione |
| TPK1thiamin pyrophosphokinase 1 | A volte (5–29%) | In 1 condizione |
| TTRtransthyretin | A volte (5–29%) | In 1 condizione |
| UFC1ubiquitin-fold modifier conjugating enzyme 1 | A volte (5–29%) | In 1 condizione |
| CAMTA1calmodulin binding transcription activator 1 | Raramente (1–4%) | In 1 condizione |
| NOP56NOP56 ribonucleoprotein | Raramente (1–4%) | In 1 condizione |
| SPTBN1spectrin beta, non-erythrocytic 1 | Raramente (1–4%) | In 1 condizione |
| GJC2gap junction protein gamma 2 | Non registrato | In 2 condizioni |
| GSSglutathione synthetase | Non registrato | In 1 condizione |
| ITM2Bintegral membrane protein 2B | Non registrato | In 1 condizione |
| KCNJ10potassium inwardly rectifying channel subfamily J member 10 | Non registrato | In 1 condizione |
| NFASCneurofascin | Non registrato | In 1 condizione |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Non registrato | In 1 condizione |
| PLA2G6phospholipase A2 group VI | Non registrato | In 1 condizione |
| PTENphosphatase and tensin homolog | Non registrato | In 1 condizione |
| TBPTATA-box binding protein | Non registrato | In 1 condizione |
| TMEM70transmembrane protein 70 | Non registrato | In 1 condizione |
| VLDLRvery low density lipoprotein receptor | Non registrato | In 1 condizione |
| VWA3Bvon Willebrand factor A domain containing 3B | Non registrato | In 1 condizione |
Con quale frequenza questo tratto si presenta tra le persone con una delle condizioni legate al gene, nella misura più alta riscontrata tra queste, secondo quanto registrato dall'Human Phenotype Ontology. Queste pagine descrivono tratti e la ricerca che li riguarda; non costituiscono una diagnosi, e per i sintomi il medico o il consulente genetico è la persona a cui rivolgersi.
Tratti più generali
Fonte dei dati
- Human Phenotype Ontology, versione 2026-09-01: il tratto, i suoi nomi, la sua definizione e i geni a esso collegati. Per saperne di più visiti hpo.jax.org.
- Versione dei dati 2026.10.18-8b139e39.
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