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Egenskap
Hand tremor
An unintentional, oscillating to-and-fro muscle movement affecting the hand.
Sammendrag
- Også kalt
- Tremor of hand, Tremor of hands, tremors in hands
- 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/hand-tremor.json"
page <- fromJSON(url)
page$trait$nameHand tremorHP:0002378
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Les genene knyttet til Hand tremor, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test38 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.
- Chung-Jansen Syndrome (PHIP)Reads 1 of these genesPHIPAbout this report →
- Jaberi-Elahi SyndromeReads 1 of these genesGTPBP2About this report →
- TRAPPC6B-Related Neurodevelopmental DisorderReads 1 of these genesTRAPPC6BAbout this report →
- Wilson DiseaseReads 1 of these genesATP7BAbout this report →
Show 34 more reports
- Rare Hereditary Peripheral NeuropathiesReads 13 of these genesSPTLC1PDK3SMN1GJB1MARS1MFN2About this report →
- Charcot-Marie-Tooth DiseaseReads 7 of these genesPDK3GJB1MARS1MFN2NEFLPMP2About this report →
- Inherited Neurodegenerative DisordersReads 14 of these genesSPTLC1SMN1CAMTA1PLA2G6POLGVRK1About this report →
- DOORS SyndromeReads 1 of these genesTBC1D24About this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 4 of these genesCAMTA1FGF14STUB1NOP56About this report →
- Disorder of Copper MetabolismReads 1 of these genesATP7BAbout this report →
- HyperthyroidismReads 1 of these genesTSHRAbout this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 3 of these genesTOR1ATAF1ANO3About this report →
- Hereditary Spastic ParaplegiaReads 4 of these genesERLIN2GBA2TFGZFYVE26About this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 2 of these genesSPTLC1NGFAbout this report →
- Surfactant Metabolism DysfunctionReads 1 of these genesMARS1About this report →
- Vanishing White Matter DiseaseReads 1 of these genesAARS2About this report →
- Spinal Muscular AtrophyReads 2 of these genesSMN1VRK1About this report →
- Basal Ganglia CalcificationReads 1 of these genesPDGFBAbout this report →
- Neurodegeneration with Brain Iron Accumulation (NBIA)Reads 1 of these genesPLA2G6About this report →
- HyperinsulinismReads 1 of these genesGCKAbout this report →
- LipodystrophyReads 1 of these genesMFN2About this report →
- Maturity-Onset Diabetes Of The YoungReads 1 of these genesGCKAbout this report →
- Parkinson DiseaseReads 1 of these genesPLA2G6About this report →
- Congenital HypothyroidismReads 1 of these genesTSHRAbout this report →
- Neonatal Diabetes MellitusReads 1 of these genesGCKAbout this report →
- Pontocerebellar Hypoplasia (TSEN54 and MINPP1)Reads 1 of these genesVRK1About this report →
- Epilepsy (Full Panel)Reads 3 of these genesCNTN2SAMD12TBC1D24About this report →
- Lissencephaly Spectrum DisordersReads 1 of these genesRAB3GAP2About this report →
- Microphthalmia, Anophthalmia & ColobomaReads 1 of these genesRAB3GAP2About this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 1 of these genesSPTLC1About this report →
- Diabetes MellitusReads 1 of these genesGCKAbout this report →
- Thyroid CancerReads 1 of these genesTSHRAbout this report →
- Primary Mitochondrial DiseaseReads 2 of these genesPOLGAARS2About this report →
- Hypogonadotropic HypogonadismReads 1 of these genesRAB3GAP2About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesSTUB1About this report →
- Intellectual DisabilityReads 2 of these genesTAF1VRK1About this report →
- Other Inherited LeukodystrophiesReads 1 of these genesAARS2About this report →
- Hearing Loss and DeafnessReads 1 of these genesTBC1D24About this report →
Les genene knyttet til Hand tremor, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test51 gener knyttet til Hand tremor
Endringer i disse genene forårsaker sjeldne tilstander der Hand tremor 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 |
|---|---|---|
| ATP7BATPase copper transporting beta | Alltid | I 1 tilstand |
| GTPBP1GTP binding protein 1 | Alltid | I 1 tilstand |
| KCNN2potassium calcium-activated channel subfamily N member 2 | Alltid | I 1 tilstand |
| LRRC7leucine rich repeat containing 7 | Alltid | I 1 tilstand |
| RAB32RAB32, member RAS oncogene family | Alltid | I 1 tilstand |
| RAB3ARAB3A, member RAS oncogene family | Alltid | I 1 tilstand |
| SLC6A17solute carrier family 6 member 17 | Alltid | I 2 tilstander |
| SPTLC1serine palmitoyltransferase long chain base subunit 1 | Alltid | I 1 tilstand |
| TOR1Atorsin family 1 member A | Alltid | I 1 tilstand |
| ADRA2Badrenoceptor alpha 2B | Svært ofte (80–99 %) | I 1 tilstand |
| CNTN2contactin 2 | Svært ofte (80–99 %) | I 1 tilstand |
| CTNND2catenin delta 2 | Svært ofte (80–99 %) | I 1 tilstand |
| MARCHF6membrane associated ring-CH-type finger 6 | Svært ofte (80–99 %) | I 1 tilstand |
| PDK3pyruvate dehydrogenase kinase 3 | Svært ofte (80–99 %) | I 2 tilstander |
| RAPGEF2Rap guanine nucleotide exchange factor 2 | Svært ofte (80–99 %) | I 1 tilstand |
| SAMD12sterile alpha motif domain containing 12 | Svært ofte (80–99 %) | I 1 tilstand |
| SMN1survival of motor neuron 1, telomeric | Svært ofte (80–99 %) | I 3 tilstander |
| TBC1D24TBC1 domain family member 24 | Svært ofte (80–99 %) | I 1 tilstand |
| TNRC6Atrinucleotide repeat containing adaptor 6A | Svært ofte (80–99 %) | I 1 tilstand |
| TSHRthyroid stimulating hormone receptor | Svært ofte (80–99 %) | I 2 tilstander |
| YEATS2YEATS domain containing 2 | Svært ofte (80–99 %) | I 1 tilstand |
| CAMTA1calmodulin binding transcription activator 1 | Ofte (30–79 %) | I 1 tilstand |
| GCKglucokinase | Ofte (30–79 %) | I 1 tilstand |
| GJB1gap junction protein beta 1 | Ofte (30–79 %) | I 1 tilstand |
| GTPBP2GTP binding protein 2 | Ofte (30–79 %) | I 1 tilstand |
| MARS1methionyl-tRNA synthetase 1 | Ofte (30–79 %) | I 1 tilstand |
| MFN2mitofusin 2 | Ofte (30–79 %) | I 1 tilstand |
| NEFLneurofilament light chain | Ofte (30–79 %) | I 1 tilstand |
| NGFnerve growth factor | Ofte (30–79 %) | I 1 tilstand |
| PLA2G6phospholipase A2 group VI | Ofte (30–79 %) | I 1 tilstand |
| PMP2peripheral myelin protein 2 | Ofte (30–79 %) | I 1 tilstand |
| POLGDNA polymerase gamma, catalytic subunit | Ofte (30–79 %) | I 1 tilstand |
| RAB3GAP2RAB3 GTPase activating non-catalytic protein subunit 2 | Ofte (30–79 %) | I 1 tilstand |
| TAF1TATA-box binding protein associated factor 1 | Ofte (30–79 %) | I 1 tilstand |
| TRAPPC6Btrafficking protein particle complex subunit 6B | Ofte (30–79 %) | I 1 tilstand |
| VRK1VRK serine/threonine kinase 1 | Ofte (30–79 %) | I 1 tilstand |
| ZFRzinc finger RNA binding protein | Ofte (30–79 %) | I 1 tilstand |
| AARS2alanyl-tRNA synthetase 2, mitochondrial | Noen ganger (5–29 %) | I 1 tilstand |
| ANO3anoctamin 3 | Noen ganger (5–29 %) | I 1 tilstand |
| ERLIN2ER lipid raft associated 2 | Noen ganger (5–29 %) | I 2 tilstander |
Vis 11 gener til
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| FGF14fibroblast growth factor 14 | Noen ganger (5–29 %) | I 1 tilstand |
| GBA2glucosylceramidase beta 2 | Noen ganger (5–29 %) | I 1 tilstand |
| PHIPPHIP subunit of CUL4-Ring ligase complex | Noen ganger (5–29 %) | I 1 tilstand |
| STUB1STIP1 homology and U-box containing protein 1 | Noen ganger (5–29 %) | I 1 tilstand |
| TFGtrafficking from ER to golgi regulator | Noen ganger (5–29 %) | I 1 tilstand |
| ZFYVE26zinc finger FYVE-type containing 26 | Noen ganger (5–29 %) | I 1 tilstand |
| NOP56NOP56 ribonucleoprotein | Sjelden (1–4%) | I 1 tilstand |
| PDGFBplatelet derived growth factor subunit B | Sjelden (1–4%) | I 1 tilstand |
| ABCB6ATP binding cassette subfamily B member 6 (LAN blood group) | Ikke registrert | I 1 tilstand |
| DRD3dopamine receptor D3 | Ikke registrert | I 1 tilstand |
| SMN2survival of motor neuron 2, centromeric | 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.
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 2026.10.19-9814e911.
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Read the genes behind these traits in your own DNA.
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