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Prolonged QT interval
Increased time between the start of the Q wave and the end of the T wave as measured by the electrocardiogram (EKG).
Resumé
- Også kaldet
- Long QT syndrome, Prolong qt interval on ekg
- Kropssystem
- Abnormality of the cardiovascular system
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Denne side som data
Tilføj .json til sidens adresse, eller bed om application/json, for at læse den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/prolonged-qt-interval.json"
page <- fromJSON(url)
page$trait$nameProlonged QT intervalHP:0001657
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Læs de gener, der er knyttet til Prolonged QT interval, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test44 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.
- Long QT SyndromeReads 7 of these genesCACNA1CKCNE1KCNH2KCNJ2CALM1KCNQ1About this report →
- Short Qt SyndromeReads 3 of these genesKCNH2KCNJ2KCNQ1About this report →
- Malignant Hyperthermia SusceptibilityReads 2 of these genesCACNA1SRYR1About this report →
- Familial Periodic ParalysisReads 2 of these genesKCNJ2CACNA1SAbout this report →
Show 40 more reports
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 3 of these genesLMNATRPM4SCN5AAbout this report →
- Familial Atrial FibrillationReads 2 of these genesKCNJ2KCNQ1About this report →
- Pseudohypoparathyroidism & GNAS-Inactivation DisordersReads 2 of these genesGNASSTX16About this report →
- Brugada SyndromeReads 1 of these genesSCN5AAbout this report →
- Congenital Central Hypoventilation SyndromeReads 1 of these genesPHOX2BAbout this report →
- DCMA Syndrome (3-Methylglutaconic Aciduria Type 5)Reads 1 of these genesDNAJC19About this report →
- Gitelman SyndromeReads 1 of these genesSLC12A3About this report →
- Simpson-Golabi-Behmel SyndromeReads 1 of these genesGPC3About this report →
- Stankiewicz-Isidor SyndromeReads 1 of these genesPSMD12About this report →
- Very Long Chain Acyl-Coa Dehydrogenase DeficiencyReads 1 of these genesACADVLAbout this report →
- Catecholaminergic Polymorphic Ventricular TachycardiaReads 2 of these genesTECRLCALM1About this report →
- Fibrodysplasia Ossificans ProgressivaReads 1 of these genesGNASAbout this report →
- Neuroblastoma Predisposition (ALK and PHOX2B)Reads 1 of these genesPHOX2BAbout this report →
- Restrictive CardiomyopathyReads 1 of these genesTNNT2About this report →
- LipodystrophyReads 2 of these genesLMNACAVIN1About this report →
- Cerebral Creatine Deficiency SyndromesReads 1 of these genesSLC6A8About this report →
- Hirschsprung Disease & Related Enteric NeurocristopathiesReads 1 of these genesPHOX2BAbout this report →
- Limb-Girdle Muscular DystrophyReads 3 of these genesCAV3GMPPBLMNAAbout this report →
- Fatty Acid Oxidation & Carnitine Cycle DisordersReads 2 of these genesACADVLHADHAbout this report →
- 46,XX Differences of Sex DevelopmentReads 1 of these genesSRYAbout this report →
- Bartter DiseaseReads 1 of these genesCLCNKBAbout this report →
- Dilated CardiomyopathyReads 3 of these genesLMNATNNT2SCN5AAbout this report →
- Congenital Myasthenic SyndromeReads 2 of these genesDPAGT1GMPPBAbout this report →
- Hypertrophic CardiomyopathyReads 3 of these genesSRYTNNT2ACADVLAbout this report →
- Left Ventricular NoncompactionReads 1 of these genesTNNT2About this report →
- Thyroid CancerReads 2 of these genesGNASSTX16About this report →
- HyperinsulinismReads 1 of these genesHADHAbout this report →
- Myofibrillar MyopathiesReads 1 of these genesRYR1About this report →
- Monogenic Hypertension & Mineralocorticoid DisordersReads 1 of these genesKCNJ5About this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 1 of these genesSRYAbout this report →
- Congenital MyopathiesReads 1 of these genesRYR1About this report →
- Congenital Disorders of GlycosylationReads 2 of these genesDPAGT1GMPPBAbout this report →
- Congenital Muscular DystrophiesReads 1 of these genesGMPPBAbout this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 1 of these genesTRPM4About this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 1 of these genesKCND3About this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesLMNAAbout this report →
- Inherited Neurodegenerative DisordersReads 2 of these genesKCND3TANGO2About this report →
- Epilepsy (Full Panel)Reads 1 of these genesGABRA3About this report →
- Rare Hereditary Peripheral NeuropathiesReads 1 of these genesLMNAAbout this report →
- Intellectual DisabilityReads 1 of these genesBPTFAbout this report →
Læs de gener, der er knyttet til Prolonged QT interval, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test40 gener knyttet til Prolonged QT interval
Ændringer i disse gener forårsager sjældne tilstande, hvor Prolonged QT interval ses. De fleste med dette træk har ingen af disse tilstande, og et gen på denne liste siger intet om nogens eget genom.
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| ALG10BALG10 alpha-1,2-glucosyltransferase B | Altid | I 1 tilstand |
| CACNA1Ccalcium voltage-gated channel subunit alpha1 C | Altid | I 2 tilstande |
| CAV3caveolin 3 | Altid | I 1 tilstand |
| KCNE1potassium voltage-gated channel subfamily E regulatory subunit 1 | Altid | I 1 tilstand |
| KCNH2potassium voltage-gated channel subfamily H member 2 | Altid | I 1 tilstand |
| TECRLtrans-2,3-enoyl-CoA reductase like | Altid | I 1 tilstand |
| PHOX2Bpaired like homeobox 2B | Meget ofte (80–99 %) | I 1 tilstand |
| CLCNKBchloride voltage-gated channel Kb | Ofte (30–79 %) | I 1 tilstand |
| DNAJC19DnaJ heat shock protein family (Hsp40) member C19 | Ofte (30–79 %) | I 2 tilstande |
| GPC3glypican 3 | Ofte (30–79 %) | I 1 tilstand |
| GPC4glypican 4 | Ofte (30–79 %) | I 1 tilstand |
| KCND3potassium voltage-gated channel subfamily D member 3 | Ofte (30–79 %) | I 1 tilstand |
| KCNJ2potassium inwardly rectifying channel subfamily J member 2 | Ofte (30–79 %) | I 2 tilstande |
| KCNJ5potassium inwardly rectifying channel subfamily J member 5 | Ofte (30–79 %) | I 2 tilstande |
| SLC12A3solute carrier family 12 member 3 | Ofte (30–79 %) | I 2 tilstande |
| SLC6A8solute carrier family 6 member 8 | Ofte (30–79 %) | I 1 tilstand |
| TANGO2transport and golgi organization 2 homolog | Ofte (30–79 %) | I 1 tilstand |
| ANK2ankyrin 2 | Nogle gange (5–29 %) | I 1 tilstand |
| BPTFbromodomain PHD finger transcription factor | Nogle gange (5–29 %) | I 1 tilstand |
| CACNA1Scalcium voltage-gated channel subunit alpha1 S | Nogle gange (5–29 %) | I 1 tilstand |
| DPAGT1dolichyl-phosphate N-acetylglucosaminephosphotransferase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| GABRA3gamma-aminobutyric acid type A receptor subunit alpha3 | Nogle gange (5–29 %) | I 1 tilstand |
| GMPPBGDP-mannose pyrophosphorylase B | Nogle gange (5–29 %) | I 1 tilstand |
| GNASGNAS complex locus | Nogle gange (5–29 %) | I 3 tilstande |
| KCNJ18potassium inwardly rectifying channel subfamily J member 18 | Nogle gange (5–29 %) | I 1 tilstand |
| LMNAlamin A/C | Nogle gange (5–29 %) | I 1 tilstand |
| PSMD12proteasome 26S subunit, non-ATPase 12 | Nogle gange (5–29 %) | I 1 tilstand |
| RYR1ryanodine receptor 1 | Nogle gange (5–29 %) | I 1 tilstand |
| SRYsex determining region Y | Nogle gange (5–29 %) | I 1 tilstand |
| STX16syntaxin 16 | Nogle gange (5–29 %) | I 1 tilstand |
| TNNT2troponin T2, cardiac type | Nogle gange (5–29 %) | I 1 tilstand |
| TRPM4transient receptor potential cation channel subfamily M member 4 | Nogle gange (5–29 %) | I 1 tilstand |
| ACADVLacyl-CoA dehydrogenase very long chain | Sjældent (1–4%) | I 1 tilstand |
| HADHhydroxyacyl-CoA dehydrogenase | Sjældent (1–4%) | I 1 tilstand |
| CALM1calmodulin 1 | Ikke registreret | I 1 tilstand |
| CAVIN1caveolae associated protein 1 | Ikke registreret | I 1 tilstand |
| KCNE2potassium voltage-gated channel subfamily E regulatory subunit 2 | Ikke registreret | I 1 tilstand |
| KCNQ1potassium voltage-gated channel subfamily Q member 1 | Ikke registreret | I 2 tilstande |
| SCN4Bsodium voltage-gated channel beta subunit 4 | Ikke registreret | I 1 tilstand |
| SCN5Asodium voltage-gated channel alpha subunit 5 | Ikke registreret | I 1 tilstand |
Hvor hyppigt det ses hos personer med en af genets tilstande, den hyppigste værdi på tværs af dem, sådan som Human Phenotype Ontology registrerer det. Disse sider beskriver egenskaber og den forskning, der ligger bag dem. De er ikke en diagnose, og hvis du har spørgsmål om symptomer, bør du spørge en læge eller genetisk rådgiver.
Snævrere træk
Bredere træk
Hvor oplysningerne kommer fra
- Human Phenotype Ontology, udgivelse 2026-09-01: egenskaben, dens navne, definition og de gener, der er knyttet til den. Læs mere på hpo.jax.org.
- Dataudgivelse 2026.10.18-8b139e39.
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