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Egenskap
Thromboembolic stroke
A cerebrovascular accident (stroke) that occurs because of thromboembolism.
Sammendrag
- Kroppssystem
- Abnormality of blood and blood-forming tissues
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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/thromboembolic-stroke.json"
page <- fromJSON(url)
page$trait$nameThromboembolic strokeHP:0001727
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Les genene knyttet til Thromboembolic stroke, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test48 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.
- Dilated CardiomyopathyReads 35 of these genesABCC9ACTC1BAG3BAG5DESDMDAbout this report →
- Left Ventricular NoncompactionReads 6 of these genesACTC1LDB3MYBPC3MYH7TNNT2TPM1About this report →
- Hypertrophic CardiomyopathyReads 16 of these genesACTC1CSRP3FLNCJPH2LDB3MYBPC3About this report →
- Familial Atrial FibrillationReads 4 of these genesKCNQ1GJA5KCNJ2MYL4About this report →
Show 44 more reports
- Myofibrillar MyopathiesReads 6 of these genesBAG3CRYABDESFLNCLDB3TTNAbout this report →
- Restrictive CardiomyopathyReads 2 of these genesTNNI3TNNT2About this report →
- Inherited Congenital Heart DefectsReads 5 of these genesACTC1GATA4GATA6MYH6NKX2-5About this report →
- Long QT SyndromeReads 4 of these genesKCNQ1KCNE1KCNJ2SCN5AAbout this report →
- Arrhythmogenic CardiomyopathyReads 4 of these genesDESDSG2DSPPLNAbout this report →
- Distal MyopathiesReads 5 of these genesCRYABFLNCLDB3MYH7TTNAbout this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 3 of these genesDESLMNASCN5AAbout this report →
- Short Qt SyndromeReads 2 of these genesKCNQ1KCNJ2About this report →
- Brugada SyndromeReads 1 of these genesSCN5AAbout this report →
- Deficiency of Adenosine Deaminase 2 (DADA2)Reads 1 of these genesADA2About this report →
- Dystrophinopathies (Duchenne and Becker Muscular Dystrophy)Reads 1 of these genesDMDAbout this report →
- Alzheimer diseaseReads 2 of these genesPSEN1PSEN2About this report →
- Limb-Girdle Muscular DystrophyReads 5 of these genesFKTNLMNASGCDTCAPTTNAbout this report →
- Syndromic and Metabolic CardiomyopathiesReads 2 of these genesACTN2NKX2-5About this report →
- Cantú SyndromeReads 1 of these genesABCC9About this report →
- Congenital MyopathiesReads 3 of these genesMYH7MYPNTTNAbout this report →
- Familial Periodic ParalysisReads 1 of these genesKCNJ2About this report →
- Tetralogy of FallotReads 1 of these genesNKX2-5About this report →
- Neonatal Diabetes MellitusReads 2 of these genesGATA4GATA6About this report →
- Diabetes MellitusReads 2 of these genesGATA4GATA6About this report →
- Familial Glucocorticoid DeficiencyReads 1 of these genesTXNRD2About this report →
- Malignant Endocrine NeoplasmReads 1 of these genesSDHAAbout this report →
- Anterior Segment Dysgenesis, Axenfeld-Rieger Syndrome & AniridiaReads 1 of these genesPITX2About this report →
- Hereditary Pheochromocytoma and ParagangliomaReads 1 of these genesSDHAAbout this report →
- LipodystrophyReads 1 of these genesLMNAAbout this report →
- Urinary and Renal System TumourReads 1 of these genesSDHAAbout this report →
- Frontotemporal DementiaReads 1 of these genesPSEN1About this report →
- Monogenic Hypertension & Mineralocorticoid DisordersReads 1 of these genesKCNJ5About this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 1 of these genesGATA4About this report →
- Epidermolysis BullosaReads 1 of these genesDSPAbout this report →
- Congenital HypothyroidismReads 1 of these genesNKX2-5About this report →
- Homocystinuria & Cobalamin DisordersReads 1 of these genesMTHFRAbout this report →
- Noonan SyndromeReads 1 of these genesRAF1About this report →
- Hereditary Congenital & Juvenile CataractReads 1 of these genesCRYABAbout this report →
- Congenital Disorders of GlycosylationReads 2 of these genesDOLKFKTNAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 3 of these genesLMNAMTHFRSDHAAbout this report →
- Congenital Muscular DystrophiesReads 1 of these genesFKTNAbout this report →
- Thyroid CancerReads 1 of these genesNKX2-5About this report →
- Rare Monogenic Autoinflammatory DiseasesReads 1 of these genesADA2About this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 1 of these genesDSPAbout this report →
- Inherited Neurodegenerative DisordersReads 3 of these genesPSEN1PSEN2SDHAAbout this report →
- Leigh SyndromeReads 1 of these genesSDHAAbout this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesLMNAAbout this report →
- Epilepsy (Full Panel)Reads 1 of these genesSCN1BAbout this report →
Les genene knyttet til Thromboembolic stroke, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test78 gener knyttet til Thromboembolic stroke
Endringer i disse genene forårsaker sjeldne tilstander der Thromboembolic stroke 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 |
|---|---|---|
| MAN2B2mannosidase alpha class 2B member 2 | Alltid | I 1 tilstand |
| ADA2adenosine deaminase 2 | Svært ofte (80–99 %) | I 1 tilstand |
| KCNQ1potassium voltage-gated channel subfamily Q member 1 | Ofte (30–79 %) | I 2 tilstander |
| ABCC9ATP binding cassette subfamily C member 9 | Noen ganger (5–29 %) | I 2 tilstander |
| ACTC1actin alpha cardiac muscle 1 | Noen ganger (5–29 %) | I 1 tilstand |
| ACTN2actinin alpha 2 | Noen ganger (5–29 %) | I 1 tilstand |
| ANKRD1ankyrin repeat domain 1 | Noen ganger (5–29 %) | I 1 tilstand |
| BAG3BAG cochaperone 3 | Noen ganger (5–29 %) | I 1 tilstand |
| BAG5BAG cochaperone 5 | Noen ganger (5–29 %) | I 1 tilstand |
| CAP2cyclase associated actin cytoskeleton regulatory protein 2 | Noen ganger (5–29 %) | I 1 tilstand |
| CRYABcrystallin alpha B | Noen ganger (5–29 %) | I 1 tilstand |
| CSRP3cysteine and glycine rich protein 3 | Noen ganger (5–29 %) | I 1 tilstand |
| DESdesmin | Noen ganger (5–29 %) | I 1 tilstand |
| DMDdystrophin | Noen ganger (5–29 %) | I 1 tilstand |
| DOLKdolichol kinase | Noen ganger (5–29 %) | I 1 tilstand |
| DSG2desmoglein 2 | Noen ganger (5–29 %) | I 1 tilstand |
| DSPdesmoplakin | Noen ganger (5–29 %) | I 1 tilstand |
| FHL2four and a half LIM domains 2 | Noen ganger (5–29 %) | I 1 tilstand |
| FKTNfukutin | Noen ganger (5–29 %) | I 1 tilstand |
| FLNCfilamin C | Noen ganger (5–29 %) | I 1 tilstand |
| GATA4GATA binding protein 4 | Noen ganger (5–29 %) | I 1 tilstand |
| GATA5GATA binding protein 5 | Noen ganger (5–29 %) | I 1 tilstand |
| GATA6GATA binding protein 6 | Noen ganger (5–29 %) | I 1 tilstand |
| GATAD1GATA zinc finger domain containing 1 | Noen ganger (5–29 %) | I 1 tilstand |
| GET3guided entry of tail-anchored proteins factor 3, ATPase | Noen ganger (5–29 %) | I 1 tilstand |
| GJA5gap junction protein alpha 5 | Noen ganger (5–29 %) | I 1 tilstand |
| HAND2heart and neural crest derivatives expressed 2 | Noen ganger (5–29 %) | I 1 tilstand |
| JPH2junctophilin 2 | Noen ganger (5–29 %) | I 1 tilstand |
| KCNA5potassium voltage-gated channel subfamily A member 5 | Noen ganger (5–29 %) | I 1 tilstand |
| KCNE1potassium voltage-gated channel subfamily E regulatory subunit 1 | Noen ganger (5–29 %) | I 1 tilstand |
| KCNE2potassium voltage-gated channel subfamily E regulatory subunit 2 | Noen ganger (5–29 %) | I 1 tilstand |
| KCNJ2potassium inwardly rectifying channel subfamily J member 2 | Noen ganger (5–29 %) | I 1 tilstand |
| KCNJ3potassium inwardly rectifying channel subfamily J member 3 | Noen ganger (5–29 %) | I 1 tilstand |
| KCNJ5potassium inwardly rectifying channel subfamily J member 5 | Noen ganger (5–29 %) | I 1 tilstand |
| LAMA4laminin subunit alpha 4 | Noen ganger (5–29 %) | I 1 tilstand |
| LDB3LIM domain binding 3 | Noen ganger (5–29 %) | I 1 tilstand |
| LMNAlamin A/C | Noen ganger (5–29 %) | I 1 tilstand |
| LMOD2leiomodin 2 | Noen ganger (5–29 %) | I 1 tilstand |
| MTHFRmethylenetetrahydrofolate reductase | Noen ganger (5–29 %) | I 1 tilstand |
| MYBPC3myosin binding protein C3 | Noen ganger (5–29 %) | I 1 tilstand |
Vis 38 gener til
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| MYH6myosin heavy chain 6 | Noen ganger (5–29 %) | I 1 tilstand |
| MYH7myosin heavy chain 7 | Noen ganger (5–29 %) | I 1 tilstand |
| MYL4myosin light chain 4 | Noen ganger (5–29 %) | I 1 tilstand |
| MYPNmyopalladin | Noen ganger (5–29 %) | I 1 tilstand |
| NEXNnexilin F-actin binding protein | Noen ganger (5–29 %) | I 1 tilstand |
| NKX2-5NK2 homeobox 5 | Noen ganger (5–29 %) | I 1 tilstand |
| NKX2-6NK2 homeobox 6 | Noen ganger (5–29 %) | I 1 tilstand |
| NPPAnatriuretic peptide A | Noen ganger (5–29 %) | I 1 tilstand |
| NRAPnebulin related anchoring protein | Noen ganger (5–29 %) | I 1 tilstand |
| NUP155nucleoporin 155 | Noen ganger (5–29 %) | I 1 tilstand |
| PITX2paired like homeodomain 2 | Noen ganger (5–29 %) | I 1 tilstand |
| PLNphospholamban | Noen ganger (5–29 %) | I 1 tilstand |
| PPCSphosphopantothenoylcysteine synthetase | Noen ganger (5–29 %) | I 1 tilstand |
| PRDM16PR/SET domain 16 | Noen ganger (5–29 %) | I 1 tilstand |
| PSEN1presenilin 1 | Noen ganger (5–29 %) | I 1 tilstand |
| PSEN2presenilin 2 | Noen ganger (5–29 %) | I 1 tilstand |
| RAF1Raf-1 proto-oncogene, serine/threonine kinase | Noen ganger (5–29 %) | I 1 tilstand |
| RBM20RNA binding motif protein 20 | Noen ganger (5–29 %) | I 1 tilstand |
| RPL3Lribosomal protein L3 like | Noen ganger (5–29 %) | I 1 tilstand |
| SCN1Bsodium voltage-gated channel beta subunit 1 | Noen ganger (5–29 %) | I 1 tilstand |
| SCN2Bsodium voltage-gated channel beta subunit 2 | Noen ganger (5–29 %) | I 1 tilstand |
| SCN3Bsodium voltage-gated channel beta subunit 3 | Noen ganger (5–29 %) | I 1 tilstand |
| SCN4Bsodium voltage-gated channel beta subunit 4 | Noen ganger (5–29 %) | I 1 tilstand |
| SCN5Asodium voltage-gated channel alpha subunit 5 | Noen ganger (5–29 %) | I 2 tilstander |
| SDHAsuccinate dehydrogenase complex flavoprotein subunit A | Noen ganger (5–29 %) | I 1 tilstand |
| SGCDsarcoglycan delta | Noen ganger (5–29 %) | I 1 tilstand |
| TAF1ATATA-box binding protein associated factor, RNA polymerase I subunit A | Noen ganger (5–29 %) | I 1 tilstand |
| TAFAZZINtafazzin, phospholipid-lysophospholipid transacylase | Noen ganger (5–29 %) | I 1 tilstand |
| TCAPtitin-cap | Noen ganger (5–29 %) | I 1 tilstand |
| TMPOthymopoietin | Noen ganger (5–29 %) | I 1 tilstand |
| TNNC1troponin C1, slow skeletal and cardiac type | Noen ganger (5–29 %) | I 1 tilstand |
| TNNI3troponin I3, cardiac type | Noen ganger (5–29 %) | I 1 tilstand |
| TNNT2troponin T2, cardiac type | Noen ganger (5–29 %) | I 1 tilstand |
| TPM1tropomyosin 1 | Noen ganger (5–29 %) | I 1 tilstand |
| TTNtitin | Noen ganger (5–29 %) | I 2 tilstander |
| TXNRD2thioredoxin reductase 2 | Noen ganger (5–29 %) | I 1 tilstand |
| VCLvinculin | Noen ganger (5–29 %) | I 1 tilstand |
| VEZF1vascular endothelial zinc finger 1 | Noen ganger (5–29 %) | 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.
The Genome Test sequences nearly all of your DNA, not a preset panel, so every gene on these pages is in your data. Premium adds 810+ physician-ready reports.
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