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Tunnus
Left ventricular hypertrophy
Enlargement or increased size of the heart left ventricle.
Kokkuvõte
- Teised nimetused
- Heart left ventricle hypertrophy, Left ventricular wall hypertrophy
- Kehasüsteem
- Abnormality of the cardiovascular system
Left ventricular hypertrophyHP:0001712
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Read the genes linked to Left ventricular hypertrophy, and the rest of your genome, with one test.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test123 geeni on seotud tunnusega Left ventricular hypertrophy
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Left ventricular hypertrophy. 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 |
|---|---|---|
| ALPK3alpha kinase 3 | Alati | Esineb 1 haiguses |
| CILK1ciliogenesis associated kinase 1 | Alati | Esineb 1 haiguses |
| COG1component of oligomeric golgi complex 1 | Alati | Esineb 1 haiguses |
| COQ9coenzyme Q9 | Alati | Esineb 1 haiguses |
| COX16cytochrome c oxidase assembly factor COX16 | Alati | Esineb 1 haiguses |
| COX18cytochrome c oxidase assembly factor COX18 | Alati | Esineb 1 haiguses |
| FZR1fizzy and cell division cycle 20 related 1 | Alati | Esineb 1 haiguses |
| INSRinsulin receptor | Alati | Esineb 1 haiguses |
| JKAMPJNK1/MAPK8 associated membrane protein | Alati | Esineb 1 haiguses |
| JPH2junctophilin 2 | Alati | Esineb 1 haiguses |
| LDB3LIM domain binding 3 | Alati | Esineb 2 haiguses |
| MYH6myosin heavy chain 6 | Alati | Esineb 1 haiguses |
| MYL3myosin light chain 3 | Alati | Esineb 1 haiguses |
| NEK8NIMA related kinase 8 | Alati | Esineb 1 haiguses |
| NEXNnexilin F-actin binding protein | Alati | Esineb 1 haiguses |
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Alati | Esineb 1 haiguses |
| PLNphospholamban | Alati | Esineb 1 haiguses |
| SCO1synthesis of cytochrome C oxidase 1 | Alati | Esineb 1 haiguses |
| SDHDsuccinate dehydrogenase complex subunit D | Alati | Esineb 2 haiguses |
| SGSM3small G protein signaling modulator 3 | Alati | Esineb 1 haiguses |
| SLC25A4solute carrier family 25 member 4 | Alati | Esineb 2 haiguses |
| TCAPtitin-cap | Alati | Esineb 1 haiguses |
| TRIM63tripartite motif containing 63 | Alati | Esineb 1 haiguses |
| AIPAHR interacting HSP90 co-chaperone | Väga sageli (80–99%) | Esineb 2 haiguses |
| GAAalpha glucosidase | Väga sageli (80–99%) | Esineb 1 haiguses |
| MEN1menin 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| MYL2myosin light chain 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| BAG3BAG cochaperone 3 | Sageli (30–79%) | Esineb 1 haiguses |
| C1QBPcomplement C1q binding protein | Sageli (30–79%) | Esineb 1 haiguses |
| CACNA1Dcalcium voltage-gated channel subunit alpha1 D | Sageli (30–79%) | Esineb 1 haiguses |
| ESPNespin | Sageli (30–79%) | Esineb 1 haiguses |
| FHL1four and a half LIM domains 1 | Sageli (30–79%) | Esineb 1 haiguses |
| HADHAhydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha | Sageli (30–79%) | Esineb 1 haiguses |
| HADHBhydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta | Sageli (30–79%) | Esineb 1 haiguses |
| MTX2metaxin 2 | Sageli (30–79%) | Esineb 1 haiguses |
| PSEN1presenilin 1 | Sageli (30–79%) | Esineb 1 haiguses |
| RIT1Ras like without CAAX 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SDHAsuccinate dehydrogenase complex flavoprotein subunit A | Sageli (30–79%) | Esineb 1 haiguses |
| SDHAF1succinate dehydrogenase complex assembly factor 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SDHBsuccinate dehydrogenase complex iron sulfur subunit B | Sageli (30–79%) | Esineb 1 haiguses |
Näita veel 83 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| SVILsupervillin | Sageli (30–79%) | Esineb 1 haiguses |
| TLL1tolloid like 1 | Sageli (30–79%) | Esineb 1 haiguses |
| TNNI3troponin I3, cardiac type | Sageli (30–79%) | Esineb 1 haiguses |
| TRMT10CtRNA methyltransferase 10C, mitochondrial RNase P subunit | Sageli (30–79%) | Esineb 1 haiguses |
| ABCA1ATP binding cassette subfamily A member 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| ACTC1actin alpha cardiac muscle 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| ACTN2actinin alpha 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ADAM17ADAM metallopeptidase domain 17 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ARSKarylsulfatase family member K | Mõnikord (5–29%) | Esineb 1 haiguses |
| ATP6AP2ATPase H+ transporting accessory protein 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| BIN1bridging integrator 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| COL1A2collagen type I alpha 2 chain | Mõnikord (5–29%) | Esineb 1 haiguses |
| CYP11B1cytochrome P450 family 11 subfamily B member 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CYP11B2cytochrome P450 family 11 subfamily B member 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DBR1debranching RNA lariats 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DMDdystrophin | Mõnikord (5–29%) | Esineb 1 haiguses |
| FBXL4F-box and leucine rich repeat protein 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| FLNCfilamin C | Mõnikord (5–29%) | Esineb 1 haiguses |
| GLAgalactosidase alpha | Mõnikord (5–29%) | Esineb 2 haiguses |
| GNPTABN-acetylglucosamine-1-phosphate transferase subunits alpha and beta | Mõnikord (5–29%) | Esineb 1 haiguses |
| GTPBP3GTP binding protein 3, mitochondrial | Mõnikord (5–29%) | Esineb 1 haiguses |
| GYS1glycogen synthase 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| HCN4hyperpolarization activated cyclic nucleotide gated potassium channel 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HSD11B2hydroxysteroid 11-beta dehydrogenase 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| KCNJ5potassium inwardly rectifying channel subfamily J member 5 | Mõnikord (5–29%) | Esineb 1 haiguses |
| LOXlysyl oxidase | Mõnikord (5–29%) | Esineb 1 haiguses |
| LRPPRCleucine rich pentatricopeptide repeat containing | Mõnikord (5–29%) | Esineb 1 haiguses |
| LZTR1leucine zipper like post translational regulator 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MOGSmannosyl-oligosaccharide glucosidase | Mõnikord (5–29%) | Esineb 1 haiguses |
| MYPNmyopalladin | Mõnikord (5–29%) | Esineb 1 haiguses |
| NAXDNAD(P)HX dehydratase | Mõnikord (5–29%) | Esineb 1 haiguses |
| NDUFS2NADH:ubiquinone oxidoreductase core subunit S2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NKX2-5NK2 homeobox 5 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NONOnon-POU domain containing octamer binding | Mõnikord (5–29%) | Esineb 1 haiguses |
| POLGDNA polymerase gamma, catalytic subunit | Mõnikord (5–29%) | Esineb 1 haiguses |
| POLG2DNA polymerase gamma 2, accessory subunit | Mõnikord (5–29%) | Esineb 1 haiguses |
| POMT1protein O-mannosyltransferase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| POMT2protein O-mannosyltransferase 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PSEN2presenilin 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RNU7-1RNA, U7 small nuclear 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Mõnikord (5–29%) | Esineb 1 haiguses |
| RYR1ryanodine receptor 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SCN5Asodium voltage-gated channel alpha subunit 5 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SMAD3SMAD family member 3 | Mõnikord (5–29%) | Esineb 2 haiguses |
| SPEGstriated muscle enriched protein kinase | Mõnikord (5–29%) | Esineb 1 haiguses |
| TNNT2troponin T2, cardiac type | Mõnikord (5–29%) | Esineb 1 haiguses |
| TPK1thiamin pyrophosphokinase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TTNtitin | Mõnikord (5–29%) | Esineb 1 haiguses |
| TTRtransthyretin | Mõnikord (5–29%) | Esineb 1 haiguses |
| TWNKtwinkle mtDNA helicase | Mõnikord (5–29%) | Esineb 1 haiguses |
| ZNF687zinc finger protein 687 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GLRX5glutaredoxin 5 | Harva (1–4%) | Esineb 1 haiguses |
| ZNF462zinc finger protein 462 | Harva (1–4%) | Esineb 1 haiguses |
| ARL6ARF like GTPase 6 | Pole registreeritud | Esineb 1 haiguses |
| B3GAT3beta-1,3-glucuronyltransferase 3 | Pole registreeritud | Esineb 1 haiguses |
| BBS1Bardet-Biedl syndrome 1 | Pole registreeritud | Esineb 1 haiguses |
| CCDC28Bcoiled-coil domain containing 28B | Pole registreeritud | Esineb 1 haiguses |
| CHST3carbohydrate sulfotransferase 3 | Pole registreeritud | Esineb 1 haiguses |
| COQ7coenzyme Q7, hydroxylase | Pole registreeritud | Esineb 1 haiguses |
| DTNAdystrobrevin alpha | Pole registreeritud | Esineb 1 haiguses |
| EPG5ectopic P-granules 5 autophagy tethering factor | Pole registreeritud | Esineb 1 haiguses |
| FKRPfukutin related protein | Pole registreeritud | Esineb 1 haiguses |
| MT-CO1mitochondrially encoded cytochrome c oxidase I | Pole registreeritud | Esineb 1 haiguses |
| MT-CO2mitochondrially encoded cytochrome c oxidase II | Pole registreeritud | Esineb 1 haiguses |
| MT-CO3mitochondrially encoded cytochrome c oxidase III | Pole registreeritud | Esineb 1 haiguses |
| MT-CYBmitochondrially encoded cytochrome b | Pole registreeritud | Esineb 1 haiguses |
| MT-ND1mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 | Pole registreeritud | Esineb 1 haiguses |
| MT-ND5mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 | Pole registreeritud | Esineb 1 haiguses |
| MT-ND6mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 | Pole registreeritud | Esineb 1 haiguses |
| MT-TCmitochondrially encoded tRNA-Cys (UGU/C) | Pole registreeritud | Esineb 1 haiguses |
| MT-TFmitochondrially encoded tRNA-Phe (UUU/C) | Pole registreeritud | Esineb 1 haiguses |
| MT-THmitochondrially encoded tRNA-His (CAU/C) | Pole registreeritud | Esineb 1 haiguses |
| MT-TKmitochondrially encoded tRNA-Lys (AAA/G) | Pole registreeritud | Esineb 1 haiguses |
| MT-TL1mitochondrially encoded tRNA-Leu (UUA/G) 1 | Pole registreeritud | Esineb 1 haiguses |
| MT-TL2mitochondrially encoded tRNA-Leu (CUN) 2 | Pole registreeritud | Esineb 1 haiguses |
| MT-TQmitochondrially encoded tRNA-Gln (CAA/G) | Pole registreeritud | Esineb 1 haiguses |
| MT-TS1mitochondrially encoded tRNA-Ser (UCN) 1 | Pole registreeritud | Esineb 1 haiguses |
| MT-TS2mitochondrially encoded tRNA-Ser (AGU/C) 2 | Pole registreeritud | Esineb 1 haiguses |
| MT-TVmitochondrially encoded tRNA-Val (GUN) | Pole registreeritud | Esineb 1 haiguses |
| MT-TWmitochondrially encoded tRNA-Trp (UGA/G) | Pole registreeritud | Esineb 1 haiguses |
| MYOZ2myozenin 2 | Pole registreeritud | Esineb 1 haiguses |
| SLC25A24solute carrier family 25 member 24 | Pole registreeritud | Esineb 1 haiguses |
| WDR35WD repeat domain 35 | 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.
Kitsamad tunnused
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 2026.10.16-c6eea6bf.
Kellele me abiks olemeMeie teadusTootedTulemused
Logi sisseKüsiAlustaalates 449 $
Üks test. Vastused kogu eluks.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast