Atlas이런 분들을 위해과학적 근거제품연구 성과
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형질
Slow movements
임상 명칭: Bradykinesia
Bradykinesia literally means slow movement, and is used clinically to denote a slowness in the execution of movement (in contrast to hypokinesia, which is used to refer to slowness in the initiation of movement).
요약
- 다른 명칭
- Slowness of movements
Atlas이런 분들을 위해과학적 근거제품연구 성과
로그인질문하기유전체를 시퀀싱하세요↗
이 페이지의 데이터
페이지 주소 끝에 .json을 붙이거나 application/json을 요청하면 JSON 형식으로 읽을 수 있습니다.
library(jsonlite)
url <- "https://dantelabs.com/traits/bradykinesia.json"
page <- fromJSON(url)
page$trait$nameSlow movementsHP:0002067
Atlas이런 분들을 위해과학적 근거제품연구 성과
로그인질문하기유전체를 시퀀싱하세요↗
55 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 15 of these genesATP13A2DNAJC6MAPTPARK7PLA2G6PRKNAbout this report →
- Basal Ganglia CalcificationReads 7 of these genesMYORGJAM2NAA60PDGFBPDGFRBSLC20A2About this report →
- Neurodegeneration with Brain Iron Accumulation (NBIA)Reads 6 of these genesATP13A2PLA2G6FTLWDR45COASYPANK2About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 10 of these genesATP1A3SLC6A3GCH1NR4A2PRKRASPRAbout this report →
Show 51 more reports
- Inherited Neurodegenerative DisordersReads 31 of these genesATP13A2ATP1A3HTTMAPTPDE8BPLA2G6About this report →
- Congenital MyopathiesReads 7 of these genesACTA1KBTBD13KLHL41MYPNNEBTPM2About this report →
- BH4 Deficiency & Monoamine Neurotransmitter DisordersReads 5 of these genesGCH1SPRTHPTSDNAJC12About this report →
- Hereditary Manganese Transporter DisordersReads 2 of these genesSLC30A10SLC39A14About this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 8 of these genesATP1A3ATXN1ATXN10PPP2R2BKCNC3ATXN2About this report →
- Epilepsy (Full Panel)Reads 17 of these genesATP1A3ATP6AP2MECP2SYNJ1FGF13GABRA1About this report →
- Neuroacanthocytosis and Huntington Disease PhenocopiesReads 2 of these genesVPS13AJPH3About this report →
- Primary Mitochondrial DiseaseReads 12 of these genesPOLGCOQ2POLG2RRM2BSLC25A4TWNKAbout this report →
- 3-Methylglutaconic Aciduria Type 8 (HTRA2)Reads 1 of these genesHTRA2About this report →
- Brain Abnormalities, Neurodegeneration and Dysosteosclerosis (BANDDOS)Reads 1 of these genesCSF1RAbout this report →
- Christianson SyndromeReads 1 of these genesSLC9A6About this report →
- Dopamine Transporter Deficiency SyndromeReads 1 of these genesSLC6A3About this report →
- Dravet SyndromeReads 1 of these genesSCN1AAbout this report →
- Fragile X SyndromeReads 1 of these genesFMR1About this report →
- Gaucher DiseaseReads 1 of these genesGBA1About this report →
- Genetic Prion Disease (incl. Fatal Familial Insomnia)Reads 1 of these genesPRNPAbout this report →
- GTP Cyclohydrolase 1 DeficiencyReads 1 of these genesGCH1About this report →
- Huntington DiseaseReads 1 of these genesHTTAbout this report →
- Rett Syndrome and MECP2-Related DisordersReads 1 of these genesMECP2About this report →
- Vici SyndromeReads 1 of these genesEPG5About this report →
- Rare Hereditary Peripheral NeuropathiesReads 13 of these genesPLA2G6POLGCOQ2RRM2BSCN9AATP5MKAbout this report →
- Fontaine Progeroid SyndromeReads 1 of these genesSLC25A4About this report →
- Hereditary FibromatosesReads 1 of these genesPDGFRBAbout this report →
- Intellectual DisabilityReads 10 of these genesAHDC1ATP6AP2MECP2RAB39BFGF13PCDH19About this report →
- Leigh SyndromeReads 5 of these genesATP5MKFARS2TACO1TTC19EARS2About this report →
- Familial Hemiplegic MigraineReads 1 of these genesSCN1AAbout this report →
- Adult-Onset Leukodystrophies (CSF1R, LMNB1, Nasu-Hakola)Reads 1 of these genesCSF1RAbout this report →
- Carney Complex & Hereditary Adrenal Cushing SyndromeReads 1 of these genesPDE8BAbout this report →
- Hereditary Episodic AtaxiasReads 1 of these genesSCN2AAbout this report →
- Hereditary Spastic ParaplegiaReads 4 of these genesATP13A2FARS2UCHL1ATL1About this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 2 of these genesSCN9AATL1About this report →
- Syndromic and Metabolic CardiomyopathiesReads 1 of these genesSLC25A4About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 3 of these genesATCAYTWNKPRDX3About this report →
- Usher SyndromeReads 1 of these genesADGRV1About this report →
- Frontotemporal DementiaReads 1 of these genesMAPTAbout this report →
- Hereditary Optic NeuropathyReads 1 of these genesATP1A3About this report →
- Female InfertilityReads 2 of these genesTWNKFMR1About this report →
- Neuronal Ceroid LipofuscinosisReads 1 of these genesATP13A2About this report →
- Hereditary Corneal DystrophiesReads 1 of these genesPRDX3About this report →
- Other Inherited LeukodystrophiesReads 2 of these genesCSF1REARS2About this report →
- Pontocerebellar Hypoplasia (TSEN54 and MINPP1)Reads 1 of these genesCOASYAbout this report →
- Hereditary Congenital & Juvenile CataractReads 1 of these genesFTLAbout this report →
- Congenital Disorders of GlycosylationReads 2 of these genesATP6AP2DHDDSAbout this report →
- Spinal Muscular AtrophyReads 1 of these genesDCTN1About this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 1 of these genesDCTN1About this report →
- Nephrotic SyndromeReads 1 of these genesPODXLAbout this report →
- Dilated CardiomyopathyReads 1 of these genesMYPNAbout this report →
- Lysosomal Storage DiseaseReads 1 of these genesGBA1About this report →
- Hypertrophic CardiomyopathyReads 1 of these genesMYPNAbout this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesDCTN1About this report →
- Retinitis PigmentosaReads 1 of these genesDHDDSAbout this report →
연관 유전자 130개: Slow movements
이 유전자들의 변화는 Slow movements 증상이 나타나는 희귀 질환을 일으킵니다. 이 형질을 가진 대부분의 사람에게는 이러한 질환이 없으며, 이 목록에 있는 유전자가 누구의 개인 유전체에 대해서도 말해 주는 것은 없습니다.
| 유전자 | 나타나는 빈도 | 질환 |
|---|---|---|
| AHDC1AT-hook DNA binding motif containing 1 | 항상 | 질환 1개에서 나타남 |
| ATP13A2ATPase cation transporting 13A2 | 항상 | 질환 4개에서 나타남 |
| ATP1A3ATPase Na+/K+ transporting subunit alpha 3 | 항상 | 질환 3개에서 나타남 |
| ATP6AP2ATPase H+ transporting accessory protein 2 | 항상 | 질환 3개에서 나타남 |
| DNAJC6DnaJ heat shock protein family (Hsp40) member C6 | 항상 | 질환 3개에서 나타남 |
| EIF2AK1eukaryotic translation initiation factor 2 alpha kinase 1 | 항상 | 질환 1개에서 나타남 |
| EPG5ectopic P-granules 5 autophagy tethering factor | 항상 | 질환 1개에서 나타남 |
| HTThuntingtin | 항상 | 질환 4개에서 나타남 |
| LRRC7leucine rich repeat containing 7 | 항상 | 질환 1개에서 나타남 |
| MAPTmicrotubule associated protein tau | 항상 | 질환 6개에서 나타남 |
| MECP2methyl-CpG binding protein 2 | 항상 | 질환 2개에서 나타남 |
| MYORGmyogenesis regulating glycosidase | 항상 | 질환 3개에서 나타남 |
| PARK7Parkinsonism associated deglycase | 항상 | 질환 2개에서 나타남 |
| PDE8Bphosphodiesterase 8B | 항상 | 질환 2개에서 나타남 |
| PET117PET117 cytochrome c oxidase chaperone | 항상 | 질환 1개에서 나타남 |
| PLA2G6phospholipase A2 group VI | 항상 | 질환 3개에서 나타남 |
| POLGDNA polymerase gamma, catalytic subunit | 항상 | 질환 4개에서 나타남 |
| PRKNparkin RBR E3 ubiquitin protein ligase | 항상 | 질환 2개에서 나타남 |
| PTRHD1peptidyl-tRNA hydrolase domain containing 1 | 항상 | 질환 1개에서 나타남 |
| RAB32RAB32, member RAS oncogene family | 항상 | 질환 1개에서 나타남 |
| RAB39BRAB39B, member RAS oncogene family | 항상 | 질환 1개에서 나타남 |
| SNCAsynuclein alpha | 항상 | 질환 4개에서 나타남 |
| SYNJ1synaptojanin 1 | 항상 | 질환 3개에서 나타남 |
| UQCRC1ubiquinol-cytochrome c reductase core protein 1 | 항상 | 질환 1개에서 나타남 |
| CHCHD2coiled-coil-helix-coiled-coil-helix domain containing 2 | 매우 자주 (80–99%) | 질환 1개에서 나타남 |
| NIT1nitrilase 1 | 매우 자주 (80–99%) | 질환 1개에서 나타남 |
| PODXLpodocalyxin like | 매우 자주 (80–99%) | 질환 2개에서 나타남 |
| SLC6A3solute carrier family 6 member 3 | 매우 자주 (80–99%) | 질환 2개에서 나타남 |
| ACTA1actin alpha 1, skeletal muscle | 자주 (30–79%) | 질환 1개에서 나타남 |
| ATCAYATCAY kinesin light chain interacting caytaxin | 자주 (30–79%) | 질환 1개에서 나타남 |
| ATXN1ataxin 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| ATXN10ataxin 10 | 자주 (30–79%) | 질환 1개에서 나타남 |
| ATXN8ataxin 8 | 자주 (30–79%) | 질환 1개에서 나타남 |
| ATXN8OSATXN8 opposite strand lncRNA | 자주 (30–79%) | 질환 2개에서 나타남 |
| CMPK2cytidine/uridine monophosphate kinase 2 | 자주 (30–79%) | 질환 1개에서 나타남 |
| COQ2coenzyme Q2, polyprenyltransferase | 자주 (30–79%) | 질환 3개에서 나타남 |
| EIF2AK2eukaryotic translation initiation factor 2 alpha kinase 2 | 자주 (30–79%) | 질환 1개에서 나타남 |
| FBXO7F-box protein 7 | 자주 (30–79%) | 질환 2개에서 나타남 |
| FGF13fibroblast growth factor 13 | 자주 (30–79%) | 질환 2개에서 나타남 |
| FTLferritin light chain | 자주 (30–79%) | 질환 2개에서 나타남 |
유전자 90개 더 보기
| 유전자 | 나타나는 빈도 | 질환 |
|---|---|---|
| GABRA1gamma-aminobutyric acid type A receptor subunit alpha1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| GABRG2gamma-aminobutyric acid type A receptor subunit gamma2 | 자주 (30–79%) | 질환 2개에서 나타남 |
| GCH1GTP cyclohydrolase 1 | 자주 (30–79%) | 질환 2개에서 나타남 |
| JAM2junctional adhesion molecule 2 | 자주 (30–79%) | 질환 3개에서 나타남 |
| KBTBD13kelch repeat and BTB domain containing 13 | 자주 (30–79%) | 질환 1개에서 나타남 |
| KLHL41kelch like family member 41 | 자주 (30–79%) | 질환 1개에서 나타남 |
| MYPNmyopalladin | 자주 (30–79%) | 질환 1개에서 나타남 |
| NAA60N-alpha-acetyltransferase 60, NatF catalytic subunit | 자주 (30–79%) | 질환 2개에서 나타남 |
| NEBnebulin | 자주 (30–79%) | 질환 1개에서 나타남 |
| NR4A2nuclear receptor subfamily 4 group A member 2 | 자주 (30–79%) | 질환 3개에서 나타남 |
| PCDH19protocadherin 19 | 자주 (30–79%) | 질환 1개에서 나타남 |
| PDGFBplatelet derived growth factor subunit B | 자주 (30–79%) | 질환 2개에서 나타남 |
| PDGFRBplatelet derived growth factor receptor beta | 자주 (30–79%) | 질환 2개에서 나타남 |
| POLG2DNA polymerase gamma 2, accessory subunit | 자주 (30–79%) | 질환 1개에서 나타남 |
| PRKAR1Bprotein kinase cAMP-dependent type I regulatory subunit beta | 자주 (30–79%) | 질환 1개에서 나타남 |
| PRKRAprotein activator of interferon induced protein kinase EIF2AK2 | 자주 (30–79%) | 질환 2개에서 나타남 |
| PRNPprion protein (Kanno blood group) | 자주 (30–79%) | 질환 3개에서 나타남 |
| PTPAprotein phosphatase 2 phosphatase activator | 자주 (30–79%) | 질환 1개에서 나타남 |
| RAB3ARAB3A, member RAS oncogene family | 자주 (30–79%) | 질환 1개에서 나타남 |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | 자주 (30–79%) | 질환 1개에서 나타남 |
| RRP12ribosomal RNA processing 12 homolog | 자주 (30–79%) | 질환 2개에서 나타남 |
| SCN1Asodium voltage-gated channel alpha subunit 1 | 자주 (30–79%) | 질환 2개에서 나타남 |
| SCN1Bsodium voltage-gated channel beta subunit 1 | 자주 (30–79%) | 질환 2개에서 나타남 |
| SCN2Asodium voltage-gated channel alpha subunit 2 | 자주 (30–79%) | 질환 2개에서 나타남 |
| SCN9Asodium voltage-gated channel alpha subunit 9 | 자주 (30–79%) | 질환 2개에서 나타남 |
| SLC20A2solute carrier family 20 member 2 | 자주 (30–79%) | 질환 2개에서 나타남 |
| SLC25A4solute carrier family 25 member 4 | 자주 (30–79%) | 질환 1개에서 나타남 |
| SLC2A3solute carrier family 2 member 3 | 자주 (30–79%) | 질환 1개에서 나타남 |
| SLC30A10solute carrier family 30 member 10 | 자주 (30–79%) | 질환 2개에서 나타남 |
| SLC39A14solute carrier family 39 member 14 | 자주 (30–79%) | 질환 2개에서 나타남 |
| SLC9A6solute carrier family 9 member A6 | 자주 (30–79%) | 질환 1개에서 나타남 |
| SPRsepiapterin reductase | 자주 (30–79%) | 질환 1개에서 나타남 |
| TAF1TATA-box binding protein associated factor 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| THtyrosine hydroxylase | 자주 (30–79%) | 질환 1개에서 나타남 |
| TPM2tropomyosin 2 | 자주 (30–79%) | 질환 1개에서 나타남 |
| TPM3tropomyosin 3 | 자주 (30–79%) | 질환 1개에서 나타남 |
| TSPOAP1TSPO associated protein 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| TWNKtwinkle mtDNA helicase | 자주 (30–79%) | 질환 1개에서 나타남 |
| WARS2tryptophanyl tRNA synthetase 2, mitochondrial | 자주 (30–79%) | 질환 1개에서 나타남 |
| WDR45WD repeat domain 45 | 자주 (30–79%) | 질환 2개에서 나타남 |
| XPR1xenotropic and polytropic retrovirus receptor 1 | 자주 (30–79%) | 질환 2개에서 나타남 |
| ATP5MKATP synthase membrane subunit k | 가끔 (5–29%) | 질환 1개에서 나타남 |
| CLTCclathrin heavy chain | 가끔 (5–29%) | 질환 1개에서 나타남 |
| DNAJC13DnaJ heat shock protein family (Hsp40) member C13 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| EIF4G1eukaryotic translation initiation factor 4 gamma 1 | 가끔 (5–29%) | 질환 2개에서 나타남 |
| FARS2phenylalanyl-tRNA synthetase 2, mitochondrial | 가끔 (5–29%) | 질환 1개에서 나타남 |
| FMR1fragile X messenger ribonucleoprotein 1 | 가끔 (5–29%) | 질환 2개에서 나타남 |
| GBA1glucosylceramidase beta 1 | 가끔 (5–29%) | 질환 2개에서 나타남 |
| GIGYF2GRB10 interacting GYF protein 2 | 가끔 (5–29%) | 질환 2개에서 나타남 |
| HTRA2HtrA serine peptidase 2 | 가끔 (5–29%) | 질환 2개에서 나타남 |
| IMPDH2inosine monophosphate dehydrogenase 2 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| KCNN2potassium calcium-activated channel subfamily N member 2 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| LRRK2leucine rich repeat kinase 2 | 가끔 (5–29%) | 질환 3개에서 나타남 |
| PIDD1p53-induced death domain protein 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| PINK1PTEN induced kinase 1 | 가끔 (5–29%) | 질환 2개에서 나타남 |
| PPP2R2Bprotein phosphatase 2 regulatory subunit Bbeta | 가끔 (5–29%) | 질환 1개에서 나타남 |
| PRDX3peroxiredoxin 3 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| PTS6-pyruvoyltetrahydropterin synthase | 가끔 (5–29%) | 질환 2개에서 나타남 |
| RRM1ribonucleotide reductase catalytic subunit M1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| TACO1translational activator of cytochrome c oxidase I | 가끔 (5–29%) | 질환 1개에서 나타남 |
| TK2thymidine kinase 2 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| TOP3ADNA topoisomerase III alpha | 가끔 (5–29%) | 질환 1개에서 나타남 |
| TTC19tetratricopeptide repeat domain 19 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| UCHL1ubiquitin C-terminal hydrolase L1 | 가끔 (5–29%) | 질환 2개에서 나타남 |
| VPS13Avacuolar protein sorting 13 homolog A | 가끔 (5–29%) | 질환 1개에서 나타남 |
| VPS13Cvacuolar protein sorting 13 homolog C | 가끔 (5–29%) | 질환 1개에서 나타남 |
| VPS35VPS35 retromer complex component | 가끔 (5–29%) | 질환 2개에서 나타남 |
| ADGRV1adhesion G protein-coupled receptor V1 | 드물게 (1–4%) | 질환 1개에서 나타남 |
| ATL1atlastin GTPase 1 | 드물게 (1–4%) | 질환 1개에서 나타남 |
| CPA6carboxypeptidase A6 | 드물게 (1–4%) | 질환 1개에서 나타남 |
| GABRDgamma-aminobutyric acid type A receptor subunit delta | 드물게 (1–4%) | 질환 1개에서 나타남 |
| HCN1hyperpolarization activated cyclic nucleotide gated potassium channel 1 | 드물게 (1–4%) | 질환 1개에서 나타남 |
| KCNC3potassium voltage-gated channel subfamily C member 3 | 드물게 (1–4%) | 질환 1개에서 나타남 |
| PRRT2proline rich transmembrane protein 2 | 드물게 (1–4%) | 질환 1개에서 나타남 |
| SLC32A1solute carrier family 32 member 1 | 드물게 (1–4%) | 질환 1개에서 나타남 |
| STX1Bsyntaxin 1B | 드물게 (1–4%) | 질환 1개에서 나타남 |
| ADH1Calcohol dehydrogenase 1C (class I), gamma polypeptide | 기록되지 않음 | 질환 1개에서 나타남 |
| ATXN2ataxin 2 | 기록되지 않음 | 질환 2개에서 나타남 |
| ATXN3ataxin 3 | 기록되지 않음 | 질환 2개에서 나타남 |
| COASYCoenzyme A synthase | 기록되지 않음 | 질환 1개에서 나타남 |
| CSF1Rcolony stimulating factor 1 receptor | 기록되지 않음 | 질환 1개에서 나타남 |
| DCTN1dynactin subunit 1 | 기록되지 않음 | 질환 1개에서 나타남 |
| DHDDSdehydrodolichyl diphosphate synthase subunit | 기록되지 않음 | 질환 1개에서 나타남 |
| DNAJC12DnaJ heat shock protein family (Hsp40) member C12 | 기록되지 않음 | 질환 1개에서 나타남 |
| EARS2glutamyl-tRNA synthetase 2, mitochondrial | 기록되지 않음 | 질환 1개에서 나타남 |
| JPH3junctophilin 3 | 기록되지 않음 | 질환 1개에서 나타남 |
| MT-TTmitochondrially encoded tRNA-Thr (ACN) | 기록되지 않음 | 질환 1개에서 나타남 |
| PANK2pantothenate kinase 2 | 기록되지 않음 | 질환 1개에서 나타남 |
| SNCAIPsynuclein alpha interacting protein | 기록되지 않음 | 질환 1개에서 나타남 |
| TBPTATA-box binding protein | 기록되지 않음 | 질환 2개에서 나타남 |
Human Phenotype Ontology가 기록한, 해당 유전자와 관련된 질환을 가진 사람들 가운데 이 특징이 나타나는 빈도입니다. 이 페이지는 특징과 그 바탕이 되는 연구를 설명하며, 진단이 아닙니다. 증상에 대해서는 의사나 유전 상담사에게 문의하시기 바랍니다.
상위 형질
출처
- Human Phenotype Ontology, 버전 2026-09-01: 특징, 명칭, 정의 및 이와 연결된 유전자입니다. 자세한 내용은 hpo.jax.org에서 확인하실 수 있습니다.
- 데이터 버전 2026.10.19-9814e911.
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