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Egenskap
Left ventricular hypertrophy
Enlargement or increased size of the heart left ventricle.
Sammendrag
- Også kalt
- Heart left ventricle hypertrophy, Left ventricular wall hypertrophy
- Kroppssystem
- Abnormality of the cardiovascular system
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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/left-ventricular-hypertrophy.json"
page <- fromJSON(url)
page$trait$nameLeft ventricular hypertrophyHP:0001712
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Les genene knyttet til Left ventricular hypertrophy, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test81 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.
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Show 77 more reports
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- Monogenic Hypertension & Mineralocorticoid DisordersReads 5 of these genesCACNA1DCYP11B1CYP11B2HSD11B2KCNJ5About this report →
- Primary Mitochondrial DiseaseReads 15 of these genesCOQ9COX16SCO1SLC25A4C1QBPTRMT10CAbout this report →
- Syndromic and Metabolic CardiomyopathiesReads 3 of these genesSLC25A4ACTN2NKX2-5About this report →
- Left Ventricular NoncompactionReads 3 of these genesLDB3ACTC1TNNT2About this report →
- Congenital MyopathiesReads 5 of these genesBIN1MYPNRYR1SPEGTTNAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 17 of these genesCOQ9HADHASDHAFBXL4GTPBP3LRPPRCAbout this report →
- Inherited Congenital Heart DefectsReads 4 of these genesMYH6TLL1ACTC1NKX2-5About this report →
- Malignant Endocrine NeoplasmReads 3 of these genesMEN1SDHASDHBAbout this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 3 of these genesCACNA1DHCN4SCN5AAbout this report →
- Brugada SyndromeReads 1 of these genesSCN5AAbout this report →
- Dystrophinopathies (Duchenne and Becker Muscular Dystrophy)Reads 1 of these genesDMDAbout this report →
- Fabry DiseaseReads 1 of these genesGLAAbout this report →
- MTX2-Related Mandibuloacral DysplasiaReads 1 of these genesMTX2About this report →
- NEK8-Related Renal-Hepatic-Pancreatic DysplasiaReads 1 of these genesNEK8About this report →
- Pompe DiseaseReads 1 of these genesGAAAbout this report →
- Short-Rib Thoracic Dysplasia 7 (WDR35)Reads 1 of these genesWDR35About this report →
- Spondyloepiphyseal Dysplasia With Congenital Joint DislocationsReads 1 of these genesCHST3About this report →
- Vici SyndromeReads 1 of these genesEPG5About this report →
- Hereditary Pheochromocytoma and ParagangliomaReads 3 of these genesSDHDSDHASDHBAbout this report →
- Alzheimer diseaseReads 2 of these genesPSEN1PSEN2About this report →
- Hereditary Optic NeuropathyReads 3 of these genesMT-ND1MT-ND5MT-ND6About this report →
- Congenital Disorders of GlycosylationReads 8 of these genesCOG1PIGAATP6AP2MOGSPOMT1POMT2About this report →
- Familial Isolated Pituitary Adenoma (FIPA / X-LAG)Reads 1 of these genesAIPAbout this report →
- Malignant Hyperthermia SusceptibilityReads 1 of these genesRYR1About this report →
- Severe Inherited Insulin ResistanceReads 1 of these genesINSRAbout this report →
- Distal MyopathiesReads 3 of these genesLDB3FLNCTTNAbout this report →
- Urinary and Renal System TumourReads 2 of these genesSDHASDHBAbout this report →
- Mucolipidoses (ML II, ML III and ML IV)Reads 1 of these genesGNPTABAbout this report →
- Tetralogy of FallotReads 1 of these genesNKX2-5About this report →
- Inherited Neurodegenerative DisordersReads 11 of these genesPSEN1SDHANAXDPOLGPSEN2RNU7-1About this report →
- Congenital Muscular DystrophiesReads 3 of these genesPOMT1POMT2FKRPAbout this report →
- Lysosomal Storage DiseaseReads 4 of these genesGAAARSKGLAGNPTABAbout this report →
- Limb-Girdle Muscular DystrophyReads 3 of these genesTCAPTTNFKRPAbout this report →
- Fatty Acid Oxidation & Carnitine Cycle DisordersReads 2 of these genesHADHAHADHBAbout this report →
- Familial Paget Disease of BoneReads 1 of these genesZNF687About this report →
- Hereditary Gastrointestinal Stromal TumourReads 1 of these genesSDHBAbout this report →
- NeurofibromatosisReads 1 of these genesLZTR1About this report →
- Thiamine Transporter and Metabolism DisordersReads 1 of these genesTPK1About this report →
- Noonan SyndromeReads 2 of these genesRIT1LZTR1About this report →
- Bardet-Biedl and Alström SyndromesReads 2 of these genesARL6BBS1About this report →
- Syndromic CraniosynostosisReads 2 of these genesZNF462WDR35About this report →
- Inflammatory Bowel Diseases (IBD)Reads 1 of these genesADAM17About this report →
- Loeys-Dietz SyndromeReads 1 of these genesSMAD3About this report →
- Congenital Adrenal HyperplasiaReads 1 of these genesCYP11B1About this report →
- Ellis-van Creveld Syndrome and Cranioectodermal DysplasiaReads 1 of these genesWDR35About this report →
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- Aicardi-Goutieres SyndromeReads 1 of these genesRNU7-1About this report →
- Hereditary Sideroblastic AnaemiasReads 1 of these genesGLRX5About this report →
- Kidney CancerReads 1 of these genesSDHBAbout this report →
- Long QT SyndromeReads 1 of these genesSCN5AAbout this report →
- Marfan Like SyndromesReads 1 of these genesSMAD3About this report →
- Arrhythmogenic CardiomyopathyReads 1 of these genesPLNAbout this report →
- HyperinsulinismReads 1 of these genesINSRAbout this report →
- Polycystic Kidney DiseaseReads 1 of these genesNEK8About this report →
- Hereditary AmyloidosisReads 1 of these genesTTRAbout this report →
- Aortic AneurysmReads 1 of these genesLOXAbout this report →
- Frontotemporal DementiaReads 1 of these genesPSEN1About this report →
- Glycogen Storage DiseaseReads 1 of these genesGYS1About this report →
- Congenital HypothyroidismReads 1 of these genesNKX2-5About this report →
- GPI Anchor Biosynthesis DefectsReads 1 of these genesPIGAAbout this report →
- Nephronophthisis and Senior-Løken SyndromeReads 1 of these genesNEK8About this report →
- Ehlers-Danlos SyndromeReads 1 of these genesCOL1A2About this report →
- Epilepsy (Full Panel)Reads 3 of these genesFZR1PIGAATP6AP2About this report →
- Diabetes MellitusReads 1 of these genesMT-TL1About this report →
- Osteogenesis ImperfectaReads 1 of these genesCOL1A2About this report →
- Rare Monogenic Autoinflammatory DiseasesReads 1 of these genesRNU7-1About this report →
- Female InfertilityReads 1 of these genesTWNKAbout this report →
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- Intellectual DisabilityReads 2 of these genesATP6AP2NONOAbout this report →
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- Hearing Loss and DeafnessReads 1 of these genesESPNAbout this report →
- Other Inborn Errors of ImmunityReads 1 of these genesRNU7-1About this report →
Les genene knyttet til Left ventricular hypertrophy, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test123 gener knyttet til Left ventricular hypertrophy
Endringer i disse genene forårsaker sjeldne tilstander der Left ventricular hypertrophy 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 |
|---|---|---|
| ALPK3alpha kinase 3 | Alltid | I 1 tilstand |
| CILK1ciliogenesis associated kinase 1 | Alltid | I 1 tilstand |
| COG1component of oligomeric golgi complex 1 | Alltid | I 1 tilstand |
| COQ9coenzyme Q9 | Alltid | I 1 tilstand |
| COX16cytochrome c oxidase assembly factor COX16 | Alltid | I 1 tilstand |
| COX18cytochrome c oxidase assembly factor COX18 | Alltid | I 1 tilstand |
| FZR1fizzy and cell division cycle 20 related 1 | Alltid | I 1 tilstand |
| INSRinsulin receptor | Alltid | I 1 tilstand |
| JKAMPJNK1/MAPK8 associated membrane protein | Alltid | I 1 tilstand |
| JPH2junctophilin 2 | Alltid | I 1 tilstand |
| LDB3LIM domain binding 3 | Alltid | I 2 tilstander |
| MYH6myosin heavy chain 6 | Alltid | I 1 tilstand |
| MYL3myosin light chain 3 | Alltid | I 1 tilstand |
| NEK8NIMA related kinase 8 | Alltid | I 1 tilstand |
| NEXNnexilin F-actin binding protein | Alltid | I 1 tilstand |
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Alltid | I 1 tilstand |
| PLNphospholamban | Alltid | I 1 tilstand |
| SCO1synthesis of cytochrome C oxidase 1 | Alltid | I 1 tilstand |
| SDHDsuccinate dehydrogenase complex subunit D | Alltid | I 2 tilstander |
| SGSM3small G protein signaling modulator 3 | Alltid | I 1 tilstand |
| SLC25A4solute carrier family 25 member 4 | Alltid | I 2 tilstander |
| TCAPtitin-cap | Alltid | I 1 tilstand |
| TRIM63tripartite motif containing 63 | Alltid | I 1 tilstand |
| AIPAHR interacting HSP90 co-chaperone | Svært ofte (80–99 %) | I 2 tilstander |
| GAAalpha glucosidase | Svært ofte (80–99 %) | I 1 tilstand |
| MEN1menin 1 | Svært ofte (80–99 %) | I 1 tilstand |
| MYL2myosin light chain 2 | Svært ofte (80–99 %) | I 1 tilstand |
| BAG3BAG cochaperone 3 | Ofte (30–79 %) | I 1 tilstand |
| C1QBPcomplement C1q binding protein | Ofte (30–79 %) | I 1 tilstand |
| CACNA1Dcalcium voltage-gated channel subunit alpha1 D | Ofte (30–79 %) | I 1 tilstand |
| ESPNespin | Ofte (30–79 %) | I 1 tilstand |
| FHL1four and a half LIM domains 1 | Ofte (30–79 %) | I 1 tilstand |
| HADHAhydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha | Ofte (30–79 %) | I 1 tilstand |
| HADHBhydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta | Ofte (30–79 %) | I 1 tilstand |
| MTX2metaxin 2 | Ofte (30–79 %) | I 1 tilstand |
| PSEN1presenilin 1 | Ofte (30–79 %) | I 1 tilstand |
| RIT1Ras like without CAAX 1 | Ofte (30–79 %) | I 1 tilstand |
| SDHAsuccinate dehydrogenase complex flavoprotein subunit A | Ofte (30–79 %) | I 1 tilstand |
| SDHAF1succinate dehydrogenase complex assembly factor 1 | Ofte (30–79 %) | I 1 tilstand |
| SDHBsuccinate dehydrogenase complex iron sulfur subunit B | Ofte (30–79 %) | I 1 tilstand |
Vis 83 gener til
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| SVILsupervillin | Ofte (30–79 %) | I 1 tilstand |
| TLL1tolloid like 1 | Ofte (30–79 %) | I 1 tilstand |
| TNNI3troponin I3, cardiac type | Ofte (30–79 %) | I 1 tilstand |
| TRMT10CtRNA methyltransferase 10C, mitochondrial RNase P subunit | Ofte (30–79 %) | I 1 tilstand |
| ABCA1ATP binding cassette subfamily A member 1 | Noen ganger (5–29 %) | I 2 tilstander |
| ACTC1actin alpha cardiac muscle 1 | Noen ganger (5–29 %) | I 2 tilstander |
| ACTN2actinin alpha 2 | Noen ganger (5–29 %) | I 1 tilstand |
| ADAM17ADAM metallopeptidase domain 17 | Noen ganger (5–29 %) | I 1 tilstand |
| ARSKarylsulfatase family member K | Noen ganger (5–29 %) | I 1 tilstand |
| ATP6AP2ATPase H+ transporting accessory protein 2 | Noen ganger (5–29 %) | I 1 tilstand |
| BIN1bridging integrator 1 | Noen ganger (5–29 %) | I 1 tilstand |
| COL1A2collagen type I alpha 2 chain | Noen ganger (5–29 %) | I 1 tilstand |
| CYP11B1cytochrome P450 family 11 subfamily B member 1 | Noen ganger (5–29 %) | I 1 tilstand |
| CYP11B2cytochrome P450 family 11 subfamily B member 2 | Noen ganger (5–29 %) | I 1 tilstand |
| DBR1debranching RNA lariats 1 | Noen ganger (5–29 %) | I 1 tilstand |
| DMDdystrophin | Noen ganger (5–29 %) | I 1 tilstand |
| FBXL4F-box and leucine rich repeat protein 4 | Noen ganger (5–29 %) | I 1 tilstand |
| FLNCfilamin C | Noen ganger (5–29 %) | I 1 tilstand |
| GLAgalactosidase alpha | Noen ganger (5–29 %) | I 2 tilstander |
| GNPTABN-acetylglucosamine-1-phosphate transferase subunits alpha and beta | Noen ganger (5–29 %) | I 1 tilstand |
| GTPBP3GTP binding protein 3, mitochondrial | Noen ganger (5–29 %) | I 1 tilstand |
| GYS1glycogen synthase 1 | Noen ganger (5–29 %) | I 2 tilstander |
| HCN4hyperpolarization activated cyclic nucleotide gated potassium channel 4 | Noen ganger (5–29 %) | I 1 tilstand |
| HSD11B2hydroxysteroid 11-beta dehydrogenase 2 | Noen ganger (5–29 %) | I 1 tilstand |
| KCNJ5potassium inwardly rectifying channel subfamily J member 5 | Noen ganger (5–29 %) | I 1 tilstand |
| LOXlysyl oxidase | Noen ganger (5–29 %) | I 1 tilstand |
| LRPPRCleucine rich pentatricopeptide repeat containing | Noen ganger (5–29 %) | I 1 tilstand |
| LZTR1leucine zipper like post translational regulator 1 | Noen ganger (5–29 %) | I 1 tilstand |
| MOGSmannosyl-oligosaccharide glucosidase | Noen ganger (5–29 %) | I 1 tilstand |
| MYPNmyopalladin | Noen ganger (5–29 %) | I 1 tilstand |
| NAXDNAD(P)HX dehydratase | Noen ganger (5–29 %) | I 1 tilstand |
| NDUFS2NADH:ubiquinone oxidoreductase core subunit S2 | Noen ganger (5–29 %) | I 1 tilstand |
| NKX2-5NK2 homeobox 5 | Noen ganger (5–29 %) | I 1 tilstand |
| NONOnon-POU domain containing octamer binding | Noen ganger (5–29 %) | I 1 tilstand |
| POLGDNA polymerase gamma, catalytic subunit | Noen ganger (5–29 %) | I 1 tilstand |
| POLG2DNA polymerase gamma 2, accessory subunit | Noen ganger (5–29 %) | I 1 tilstand |
| POMT1protein O-mannosyltransferase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| POMT2protein O-mannosyltransferase 2 | Noen ganger (5–29 %) | I 1 tilstand |
| PSEN2presenilin 2 | Noen ganger (5–29 %) | I 1 tilstand |
| RNU7-1RNA, U7 small nuclear 1 | Noen ganger (5–29 %) | I 1 tilstand |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Noen ganger (5–29 %) | I 1 tilstand |
| RYR1ryanodine receptor 1 | Noen ganger (5–29 %) | I 1 tilstand |
| SCN5Asodium voltage-gated channel alpha subunit 5 | Noen ganger (5–29 %) | I 1 tilstand |
| SMAD3SMAD family member 3 | Noen ganger (5–29 %) | I 2 tilstander |
| SPEGstriated muscle enriched protein kinase | Noen ganger (5–29 %) | I 1 tilstand |
| TNNT2troponin T2, cardiac type | Noen ganger (5–29 %) | I 1 tilstand |
| TPK1thiamin pyrophosphokinase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| TTNtitin | Noen ganger (5–29 %) | I 1 tilstand |
| TTRtransthyretin | Noen ganger (5–29 %) | I 1 tilstand |
| TWNKtwinkle mtDNA helicase | Noen ganger (5–29 %) | I 1 tilstand |
| ZNF687zinc finger protein 687 | Noen ganger (5–29 %) | I 1 tilstand |
| GLRX5glutaredoxin 5 | Sjelden (1–4%) | I 1 tilstand |
| ZNF462zinc finger protein 462 | Sjelden (1–4%) | I 1 tilstand |
| ARL6ARF like GTPase 6 | Ikke registrert | I 1 tilstand |
| B3GAT3beta-1,3-glucuronyltransferase 3 | Ikke registrert | I 1 tilstand |
| BBS1Bardet-Biedl syndrome 1 | Ikke registrert | I 1 tilstand |
| CCDC28Bcoiled-coil domain containing 28B | Ikke registrert | I 1 tilstand |
| CHST3carbohydrate sulfotransferase 3 | Ikke registrert | I 1 tilstand |
| COQ7coenzyme Q7, hydroxylase | Ikke registrert | I 1 tilstand |
| DTNAdystrobrevin alpha | Ikke registrert | I 1 tilstand |
| EPG5ectopic P-granules 5 autophagy tethering factor | Ikke registrert | I 1 tilstand |
| FKRPfukutin related protein | Ikke registrert | I 1 tilstand |
| MT-CO1mitochondrially encoded cytochrome c oxidase I | Ikke registrert | I 1 tilstand |
| MT-CO2mitochondrially encoded cytochrome c oxidase II | Ikke registrert | I 1 tilstand |
| MT-CO3mitochondrially encoded cytochrome c oxidase III | Ikke registrert | I 1 tilstand |
| MT-CYBmitochondrially encoded cytochrome b | Ikke registrert | I 1 tilstand |
| MT-ND1mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 | Ikke registrert | I 1 tilstand |
| MT-ND5mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 | Ikke registrert | I 1 tilstand |
| MT-ND6mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 | Ikke registrert | I 1 tilstand |
| MT-TCmitochondrially encoded tRNA-Cys (UGU/C) | Ikke registrert | I 1 tilstand |
| MT-TFmitochondrially encoded tRNA-Phe (UUU/C) | Ikke registrert | I 1 tilstand |
| MT-THmitochondrially encoded tRNA-His (CAU/C) | Ikke registrert | I 1 tilstand |
| MT-TKmitochondrially encoded tRNA-Lys (AAA/G) | Ikke registrert | I 1 tilstand |
| MT-TL1mitochondrially encoded tRNA-Leu (UUA/G) 1 | Ikke registrert | I 1 tilstand |
| MT-TL2mitochondrially encoded tRNA-Leu (CUN) 2 | Ikke registrert | I 1 tilstand |
| MT-TQmitochondrially encoded tRNA-Gln (CAA/G) | Ikke registrert | I 1 tilstand |
| MT-TS1mitochondrially encoded tRNA-Ser (UCN) 1 | Ikke registrert | I 1 tilstand |
| MT-TS2mitochondrially encoded tRNA-Ser (AGU/C) 2 | Ikke registrert | I 1 tilstand |
| MT-TVmitochondrially encoded tRNA-Val (GUN) | Ikke registrert | I 1 tilstand |
| MT-TWmitochondrially encoded tRNA-Trp (UGA/G) | Ikke registrert | I 1 tilstand |
| MYOZ2myozenin 2 | Ikke registrert | I 1 tilstand |
| SLC25A24solute carrier family 25 member 24 | Ikke registrert | I 1 tilstand |
| WDR35WD repeat domain 35 | Ikke registrert | 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.
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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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