AtlasPožymis
Cardiac conduction abnormality
Any anomaly of the progression of electrical impulses through the heart.
Santrauka
- Taip pat vadinama
- Abnormality of cardiac conduction, Abnormality of cardiac conduction system, Cardiac conduction abnormalities, Cardiac conduction defects, Heart conduction disorder
- Kūno sistema
- Abnormality of the cardiovascular system
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Norėdami perskaityti jį kaip JSON, pridėkite .json prie puslapio adreso arba nurodykite application/json.
library(jsonlite)
url <- "https://dantelabs.com/traits/cardiac-conduction-abnormality.json"
page <- fromJSON(url)
page$trait$nameVienu tyrimu sužinokite genus, susijusius su Cardiac conduction abnormality, ir kitą jūsų genomo dalį.
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Įsigyti savo Genome Test24 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.
- Hereditary Episodic AtaxiasReads 3 of these genesCACNA1ASCN2ASLC1A3About this report →
- Hereditary Optic NeuropathyReads 5 of these genesATP1A3MT-ND1MT-ND4MT-ND5MT-ND6About this report →
- Familial Hemiplegic MigraineReads 2 of these genesATP1A2CACNA1AAbout this report →
- ATP1A2-Related Fetal Akinesia with PolymicrogyriaReads 1 of these genesATP1A2About this report →
Show 20 more reports
- Brugada SyndromeReads 1 of these genesSCN5AAbout this report →
- Leigh SyndromeReads 8 of these genesMT-ATP6MT-ND1MT-ND3MT-ND4MT-ND5MT-ND6About this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 2 of these genesLMNASCN5AAbout this report →
- Myotonic DystrophyReads 1 of these genesCNBPAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 9 of these genesLMNAMT-ATP6MT-ND1MT-ND3MT-ND4MT-ND5About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 3 of these genesATP1A3SLC2A1CLCN1About this report →
- Congenital MyopathiesReads 2 of these genesACTA1SELENONAbout this report →
- Epilepsy (Full Panel)Reads 6 of these genesATP1A2ATP1A3CACNA1ARHOBTB2SCN2ASLC2A1About this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 2 of these genesATP1A3CACNA1AAbout this report →
- Complex Neurodevelopmental Disorder With Motor FeaturesReads 1 of these genesCACNA1AAbout this report →
- Long QT SyndromeReads 1 of these genesSCN5AAbout this report →
- Inherited Neurodegenerative DisordersReads 6 of these genesATP1A3CACNA1AMT-ND1MT-ND4MT-ND5MT-ND6About this report →
- LipodystrophyReads 1 of these genesLMNAAbout this report →
- Dilated CardiomyopathyReads 2 of these genesLMNASCN5AAbout this report →
- Inherited Congenital Heart DefectsReads 1 of these genesTBX5About this report →
- Intellectual DisabilityReads 3 of these genesCREBBPEP300SCN2AAbout this report →
- Congenital Muscular DystrophiesReads 1 of these genesSELENONAbout this report →
- Diabetes MellitusReads 1 of these genesMT-TL1About this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesLMNAAbout this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesLMNAAbout this report →
Vienu tyrimu sužinokite genus, susijusius su Cardiac conduction abnormality, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test38 genų susiję su Cardiac conduction abnormality
Šių genų pakitimai sukelia retas ligas, kuriose pasireiškia Cardiac conduction abnormality. Dauguma žmonių, turinčių šį požymį, neturi nė vienos iš tų ligų, o šiame sąraše esantis genas nieko nesako apie kieno nors paties genomą.
| Genas | Kaip dažnai pasireiškia | Ligos |
|---|---|---|
| LMNAlamin A/C | Labai dažnai (80–99%) | 1 ligoje |
| NPPAnatriuretic peptide A | Labai dažnai (80–99%) | 1 ligoje |
| SCN5Asodium voltage-gated channel alpha subunit 5 | Labai dažnai (80–99%) | 1 ligoje |
| ACTA1actin alpha 1, skeletal muscle | Dažnai (30–79%) | 1 ligoje |
| CITED2Cbp/p300 interacting transactivator with ED-rich tail 2 | Dažnai (30–79%) | 1 ligoje |
| SELENONselenoprotein N | Dažnai (30–79%) | 1 ligoje |
| TBX5T-box transcription factor 5 | Dažnai (30–79%) | 1 ligoje |
| ATP1A2ATPase Na+/K+ transporting subunit alpha 2 | Kartais (5–29%) | 1 ligoje |
| ATP1A3ATPase Na+/K+ transporting subunit alpha 3 | Kartais (5–29%) | 1 ligoje |
| CACNA1Acalcium voltage-gated channel subunit alpha1 A | Kartais (5–29%) | 1 ligoje |
| CNBPCCHC-type zinc finger nucleic acid binding protein | Kartais (5–29%) | 1 ligoje |
| CREBBPCREB binding lysine acetyltransferase | Kartais (5–29%) | 2 ligose |
| EP300EP300 lysine acetyltransferase | Kartais (5–29%) | 1 ligoje |
| MT-ATP6mitochondrially encoded ATP synthase membrane subunit 6 | Kartais (5–29%) | 1 ligoje |
| MT-CO1mitochondrially encoded cytochrome c oxidase I | Kartais (5–29%) | 1 ligoje |
| MT-CO2mitochondrially encoded cytochrome c oxidase II | Kartais (5–29%) | 1 ligoje |
| MT-CO3mitochondrially encoded cytochrome c oxidase III | Kartais (5–29%) | 1 ligoje |
| MT-ND1mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 | Kartais (5–29%) | 2 ligose |
| MT-ND2mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 | Kartais (5–29%) | 1 ligoje |
| MT-ND3mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 | Kartais (5–29%) | 1 ligoje |
| MT-ND4mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 | Kartais (5–29%) | 2 ligose |
| MT-ND5mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 | Kartais (5–29%) | 2 ligose |
| MT-ND6mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 | Kartais (5–29%) | 2 ligose |
| MT-TFmitochondrially encoded tRNA-Phe (UUU/C) | Kartais (5–29%) | 1 ligoje |
| MT-THmitochondrially encoded tRNA-His (CAU/C) | Kartais (5–29%) | 1 ligoje |
| MT-TKmitochondrially encoded tRNA-Lys (AAA/G) | Kartais (5–29%) | 1 ligoje |
| MT-TL1mitochondrially encoded tRNA-Leu (UUA/G) 1 | Kartais (5–29%) | 2 ligose |
| MT-TL2mitochondrially encoded tRNA-Leu (CUN) 2 | Kartais (5–29%) | 1 ligoje |
| MT-TQmitochondrially encoded tRNA-Gln (CAA/G) | Kartais (5–29%) | 1 ligoje |
| MT-TS1mitochondrially encoded tRNA-Ser (UCN) 1 | Kartais (5–29%) | 1 ligoje |
| MT-TS2mitochondrially encoded tRNA-Ser (AGU/C) 2 | Kartais (5–29%) | 1 ligoje |
| MT-TVmitochondrially encoded tRNA-Val (GUN) | Kartais (5–29%) | 1 ligoje |
| MT-TWmitochondrially encoded tRNA-Trp (UGA/G) | Kartais (5–29%) | 2 ligose |
| RHOBTB2Rho related BTB domain containing 2 | Kartais (5–29%) | 1 ligoje |
| SCN2Asodium voltage-gated channel alpha subunit 2 | Kartais (5–29%) | 1 ligoje |
| SLC1A3solute carrier family 1 member 3 | Kartais (5–29%) | 1 ligoje |
| SLC2A1solute carrier family 2 member 1 | Kartais (5–29%) | 1 ligoje |
| CLCN1chloride voltage-gated channel 1 | Retai (1–4 %) | 1 ligoje |
Kaip dažnai šis požymis pasitaiko žmonėms, turintiems vieną iš geno sukeliamų ligų, ir kuris dažnis tarp jų didžiausias, pagal Žmogaus fenotipo ontologijos duomenis. Šiuose puslapiuose aprašomi požymiai ir juos grindžiantys tyrimai; tai nėra diagnozė, o su simptomais kreipkitės į gydytoją ar genetikos konsultantą.
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Iš kur tai žinoma
- Žmogaus fenotipo ontologija, 2026-09-01 leidimas: požymis, jo pavadinimai, apibrėžimas ir su juo susiję genai. Daugiau sužinokite svetainėje hpo.jax.org.
- Duomenų leidimas 2026.10.21-777c9289.
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