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Tunnus
Complete right bundle branch block
A conduction block of the right branch of the bundle of His. This manifests as a prolongation of the QRS complex (greater than 0.12 s) with delayed activation of the right ventricle and terminal delay on the EKG.
Kokkuvõte
- Teised nimetused
- Right bundle branch block, Right bundle-branch block
- Kehasüsteem
- Abnormality of the cardiovascular system
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Selle lehe andmed
Lehe aadressile saab lisada .json või päringusse application/json, et lugeda seda JSON-vormingus.
library(jsonlite)
url <- "https://dantelabs.com/traits/complete-right-bundle-branch-block.json"
page <- fromJSON(url)
page$trait$nameComplete right bundle branch blockHP:0011712
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Lugege välja geenid, mis on seotud Complete right bundle branch block-ga, ja kogu ülejäänud genoom ühe testiga.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test35 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 11 of these genesLMOD2TNNC1ABCC9MYH7SCN5AACTC1About this report →
- Left Ventricular NoncompactionReads 4 of these genesMYH7ACTC1TNNT2MYBPC3About this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 4 of these genesHCN4SCN5ATRPM4TNNI3KAbout this report →
- Cantú SyndromeReads 2 of these genesABCC9KCNJ8About this report →
Show 31 more reports
- Hypertrophic CardiomyopathyReads 8 of these genesMYH6TNNC1MYH7PPP1CBACTC1FLNCAbout this report →
- Brugada SyndromeReads 1 of these genesSCN5AAbout this report →
- PLEC-Related Epidermolysis Bullosa and Muscular DystrophyReads 1 of these genesPLECAbout this report →
- Polyglucosan Body Myopathy 2 (GYG1)Reads 1 of these genesGYG1About this report →
- Arrhythmogenic CardiomyopathyReads 3 of these genesPKP2DSG2JUPAbout this report →
- Inherited Congenital Heart DefectsReads 3 of these genesMYH6TLL1ACTC1About this report →
- Myotonic DystrophyReads 1 of these genesCNBPAbout this report →
- Restrictive CardiomyopathyReads 1 of these genesTNNT2About this report →
- Distal MyopathiesReads 3 of these genesMYH7DYSFFLNCAbout this report →
- Long QT SyndromeReads 2 of these genesCACNA1CSCN5AAbout this report →
- Epidermolysis BullosaReads 2 of these genesPLECJUPAbout this report →
- Heritable Pulmonary Arterial Hypertension (HPAH)Reads 1 of these genesKCNK3About this report →
- Limb-Girdle Muscular DystrophyReads 2 of these genesDYSFPLECAbout this report →
- Congenital Anomalies of the Kidney and Urinary TractReads 1 of these genesSOX17About this report →
- Hypogonadotropic HypogonadismReads 2 of these genesSEMA3ASMCHD1About this report →
- Myofibrillar MyopathiesReads 1 of these genesFLNCAbout this report →
- Monogenic Hypertension & Mineralocorticoid DisordersReads 1 of these genesSCNN1AAbout this report →
- Cutis LaxaReads 1 of these genesATP6V1E1About this report →
- Congenital MyopathiesReads 1 of these genesMYH7About this report →
- Noonan SyndromeReads 1 of these genesPPP1CBAbout this report →
- Dyskeratosis CongenitaReads 1 of these genesDNMT3BAbout this report →
- Hereditary Congenital & Juvenile CataractReads 1 of these genesLEMD2About this report →
- Congenital Myasthenic SyndromeReads 1 of these genesPLECAbout this report →
- Congenital Muscular DystrophiesReads 1 of these genesPOMT2About 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 →
- Congenital Disorders of GlycosylationReads 1 of these genesPOMT2About this report →
- Primary Mitochondrial DiseaseReads 1 of these genesRNASEH1About this report →
- Epilepsy (Full Panel)Reads 1 of these genesSCN1BAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 1 of these genesSCN10AAbout this report →
- Inherited Neurodegenerative DisordersReads 1 of these genesKCND3About this report →
Lugege välja geenid, mis on seotud Complete right bundle branch block-ga, ja kogu ülejäänud genoom ühe testiga.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test58 geeni on seotud tunnusega Complete right bundle branch block
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Complete right bundle branch block. Enamikul selle tunnusega inimestest ei ole ühtegi neist haigustest. Selles loendis olev geen ei ütle midagi kellegi enda genoomi kohta.
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| BANF1barrier to autointegration nuclear assembly factor 1 | Alati | Esineb 1 haiguses |
| CNBPCCHC-type zinc finger nucleic acid binding protein | Alati | Esineb 1 haiguses |
| EXOSC5exosome component 5 | Alati | Esineb 1 haiguses |
| GYG1glycogenin 1 | Alati | Esineb 2 haiguses |
| HCN4hyperpolarization activated cyclic nucleotide gated potassium channel 4 | Alati | Esineb 2 haiguses |
| LMOD2leiomodin 2 | Alati | Esineb 1 haiguses |
| MYH6myosin heavy chain 6 | Alati | Esineb 1 haiguses |
| POMT2protein O-mannosyltransferase 2 | Alati | Esineb 2 haiguses |
| TNNC1troponin C1, slow skeletal and cardiac type | Alati | Esineb 1 haiguses |
| ABCC9ATP binding cassette subfamily C member 9 | Sageli (30–79%) | Esineb 1 haiguses |
| AKAP9A-kinase anchoring protein 9 | Sageli (30–79%) | Esineb 1 haiguses |
| CACNA1Ccalcium voltage-gated channel subunit alpha1 C | Sageli (30–79%) | Esineb 1 haiguses |
| CACNA2D1calcium voltage-gated channel auxiliary subunit alpha2delta 1 | Sageli (30–79%) | Esineb 1 haiguses |
| CACNB2calcium voltage-gated channel auxiliary subunit beta 2 | Sageli (30–79%) | Esineb 1 haiguses |
| DNMT3BDNA methyltransferase 3 beta | Sageli (30–79%) | Esineb 1 haiguses |
| DUX4double homeobox 4 | Sageli (30–79%) | Esineb 1 haiguses |
| DUX4L1double homeobox 4 like 1 (pseudogene) | Sageli (30–79%) | Esineb 1 haiguses |
| FRG1FSHD region gene 1 | Sageli (30–79%) | Esineb 1 haiguses |
| GPD1Lglycerol-3-phosphate dehydrogenase 1 like | Sageli (30–79%) | Esineb 2 haiguses |
| KCND3potassium voltage-gated channel subfamily D member 3 | Sageli (30–79%) | Esineb 1 haiguses |
| KCNE3potassium voltage-gated channel subfamily E regulatory subunit 3 | Sageli (30–79%) | Esineb 1 haiguses |
| KCNE5potassium voltage-gated channel subfamily E regulatory subunit 5 | Sageli (30–79%) | Esineb 1 haiguses |
| KCNJ8potassium inwardly rectifying channel subfamily J member 8 | Sageli (30–79%) | Esineb 1 haiguses |
| LEMD2LEM domain nuclear envelope protein 2 | Sageli (30–79%) | Esineb 1 haiguses |
| MYH7myosin heavy chain 7 | Sageli (30–79%) | Esineb 2 haiguses |
| NPPAnatriuretic peptide A | Sageli (30–79%) | Esineb 1 haiguses |
| PKP2plakophilin 2 | Sageli (30–79%) | Esineb 1 haiguses |
| PPP1CBprotein phosphatase 1 catalytic subunit beta | Sageli (30–79%) | Esineb 1 haiguses |
| RANGRFRAN guanine nucleotide release factor | Sageli (30–79%) | Esineb 1 haiguses |
| SCN10Asodium voltage-gated channel alpha subunit 10 | Sageli (30–79%) | Esineb 1 haiguses |
| SCN1Bsodium voltage-gated channel beta subunit 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SCN2Bsodium voltage-gated channel beta subunit 2 | Sageli (30–79%) | Esineb 1 haiguses |
| SCN3Bsodium voltage-gated channel beta subunit 3 | Sageli (30–79%) | Esineb 1 haiguses |
| SCN5Asodium voltage-gated channel alpha subunit 5 | Sageli (30–79%) | Esineb 5 haiguses |
| SCNN1Asodium channel epithelial 1 subunit alpha | Sageli (30–79%) | Esineb 1 haiguses |
| SEMA3Asemaphorin 3A | Sageli (30–79%) | Esineb 1 haiguses |
| SLMAPsarcolemma associated protein | Sageli (30–79%) | Esineb 1 haiguses |
| SMCHD1structural maintenance of chromosomes flexible hinge domain containing 1 | Sageli (30–79%) | Esineb 1 haiguses |
| TLL1tolloid like 1 | Sageli (30–79%) | Esineb 1 haiguses |
| TRPM4transient receptor potential cation channel subfamily M member 4 | Sageli (30–79%) | Esineb 2 haiguses |
Näita veel 18 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| ACTC1actin alpha cardiac muscle 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CITED2Cbp/p300 interacting transactivator with ED-rich tail 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DSG2desmoglein 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DYSFdysferlin | Mõnikord (5–29%) | Esineb 1 haiguses |
| FHL1four and a half LIM domains 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| FLNCfilamin C | Mõnikord (5–29%) | Esineb 1 haiguses |
| KCNK3potassium two pore domain channel subfamily K member 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-CYBmitochondrially encoded cytochrome b | Mõnikord (5–29%) | Esineb 1 haiguses |
| PIGUphosphatidylinositol glycan anchor biosynthesis class U | Mõnikord (5–29%) | Esineb 1 haiguses |
| RNASEH1ribonuclease H1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SOX17SRY-box transcription factor 17 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TNNT2troponin T2, cardiac type | Mõnikord (5–29%) | Esineb 1 haiguses |
| PLECplectin | Harva (1–4%) | Esineb 1 haiguses |
| ATP6V1E1ATPase H+ transporting V1 subunit E1 | Pole registreeritud | Esineb 1 haiguses |
| GNAI2G protein subunit alpha i2 | Pole registreeritud | Esineb 1 haiguses |
| JUPjunction plakoglobin | Pole registreeritud | Esineb 1 haiguses |
| MYBPC3myosin binding protein C3 | Pole registreeritud | Esineb 1 haiguses |
| TNNI3KTNNI3 interacting kinase | Pole registreeritud | Esineb 1 haiguses |
Kui sageli see esineb geenist tulenevate seisunditega inimeste seas, kõige sagedamini nende kõigi seas, nagu on märgitud Inimese fenotüübi ontoloogias. Need lehed kirjeldavad tunnuseid ja nende taga olevaid uuringuid; need ei ole diagnoos ning sümptomite kohta tuleks küsida arstilt või geneetilt nõustajalt.
Laiemad tunnused
Allikas
- Inimese fenotüübi ontoloogia, versioon 2026-09-01: tunnus, selle nimetused, määratlus ja sellega seotud geenid. Lisateave leiab aadressilt hpo.jax.org.
- Andmeversioon 2026.10.19-9814e911.
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