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Tunnus
Angina pectoris
Paroxysmal chest pain that occurs with exertion or stress and is related to myocardial ischemia.
Kokkuvõte
- 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/angina-pectoris.json"
page <- fromJSON(url)
page$trait$nameAngina pectorisHP:0001681
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Lugege välja geenid, mis on seotud Angina pectoris-ga, ja kogu ülejäänud genoom ühe testiga.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test38 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.
- HyperlipidemiaReads 8 of these genesABCG5ABCG8APOBLDLRLDLRAP1LIPCAbout this report →
- Familial HypercholesterolemiaReads 4 of these genesAPOBLDLRLDLRAP1PCSK9About this report →
- Hereditary HypolipoproteinemiasReads 4 of these genesABCA1APOA1APOBLCATAbout this report →
- Hereditary Arterial CalcificationReads 2 of these genesABCC6ENPP1About this report →
Show 34 more reports
- Cerebrotendinous XanthomatosisReads 1 of these genesCYP27A1About this report →
- Fabry DiseaseReads 1 of these genesGLAAbout this report →
- Hereditary Thrombocythaemia (JAK2)Reads 1 of these genesJAK2About this report →
- Mucopolysaccharidosis Type I (Hurler and Scheie Syndromes)Reads 1 of these genesIDUAAbout this report →
- Restrictive Dermopathy (ZMPSTE24)Reads 1 of these genesZMPSTE24About this report →
- Left Ventricular NoncompactionReads 2 of these genesTNNT2ACTC1About this report →
- Dilated CardiomyopathyReads 5 of these genesJPH2TNNC1TNNT2ACTC1LMNAAbout this report →
- Cowden Syndrome (PTEN hamartoma tumour syndrome)Reads 1 of these genesPTENAbout this report →
- Pseudoxanthoma ElasticumReads 1 of these genesABCC6About this report →
- Restrictive CardiomyopathyReads 1 of these genesTNNT2About this report →
- Hypertrophic CardiomyopathyReads 5 of these genesJPH2TNNC1TNNT2ACTC1TRIM63About this report →
- Hereditary AmyloidosisReads 2 of these genesAPOA1TTRAbout this report →
- LipodystrophyReads 2 of these genesLMNAZMPSTE24About this report →
- Inherited Congenital Heart DefectsReads 2 of these genesELNACTC1About this report →
- Lysosomal Storage DiseaseReads 4 of these genesPNPLA2GLAIDUACYP27A1About this report →
- Alzheimer diseaseReads 1 of these genesAPOEAbout this report →
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 1 of these genesCTLA4About this report →
- IPEX Syndrome and Other TregopathiesReads 1 of these genesCTLA4About this report →
- Hereditary Rickets (Hypophosphatemic and Vitamin D-Dependent)Reads 1 of these genesENPP1About this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesLMNAAbout this report →
- Epiphyseal and Spondyloepiphyseal DysplasiasReads 1 of these genesXYLT1About this report →
- HyperinsulinismReads 1 of these genesPMM2About this report →
- Rare Hereditary Peripheral NeuropathiesReads 4 of these genesAPOA1TTRLMNACYP27A1About this report →
- Cutis LaxaReads 1 of these genesELNAbout this report →
- Autoimmune DiseaseReads 1 of these genesCTLA4About this report →
- VitreoretinopathyReads 1 of these genesXYLT2About this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesLMNAAbout this report →
- Osteogenesis ImperfectaReads 1 of these genesXYLT2About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesCYP27A1About this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesLMNAAbout this report →
- Other Inherited LeukodystrophiesReads 1 of these genesCYP27A1About this report →
- Inherited Neurodegenerative DisordersReads 2 of these genesAPOECYP27A1About this report →
- Congenital Disorders of GlycosylationReads 1 of these genesPMM2About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesCTLA4About this report →
Lugege välja geenid, mis on seotud Angina pectoris-ga, ja kogu ülejäänud genoom ühe testiga.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test36 geeni on seotud tunnusega Angina pectoris
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Angina pectoris. 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 |
|---|---|---|
| JAK2Janus kinase 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| ABCA1ATP binding cassette subfamily A member 1 | Sageli (30–79%) | Esineb 1 haiguses |
| ABCG5ATP binding cassette subfamily G member 5 | Sageli (30–79%) | Esineb 1 haiguses |
| ABCG8ATP binding cassette subfamily G member 8 | Sageli (30–79%) | Esineb 1 haiguses |
| APOA1apolipoprotein A1 | Sageli (30–79%) | Esineb 1 haiguses |
| APOBapolipoprotein B | Sageli (30–79%) | Esineb 1 haiguses |
| ELNelastin | Sageli (30–79%) | Esineb 1 haiguses |
| JPH2junctophilin 2 | Sageli (30–79%) | Esineb 1 haiguses |
| LDLRlow density lipoprotein receptor | Sageli (30–79%) | Esineb 1 haiguses |
| LDLRAP1low density lipoprotein receptor adaptor protein 1 | Sageli (30–79%) | Esineb 1 haiguses |
| LIPClipase C, hepatic type | Sageli (30–79%) | Esineb 2 haiguses |
| PCSK9proprotein convertase subtilisin/kexin type 9 | Sageli (30–79%) | Esineb 1 haiguses |
| PNPLA2patatin like domain 2, triacylglycerol lipase | Sageli (30–79%) | Esineb 1 haiguses |
| TNNC1troponin C1, slow skeletal and cardiac type | Sageli (30–79%) | Esineb 1 haiguses |
| TNNT2troponin T2, cardiac type | Sageli (30–79%) | Esineb 1 haiguses |
| ABCC6ATP binding cassette subfamily C member 6 | Mõnikord (5–29%) | Esineb 3 haiguses |
| ACTC1actin alpha cardiac muscle 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| APOEapolipoprotein E | Mõnikord (5–29%) | Esineb 1 haiguses |
| CTLA4cytotoxic T-lymphocyte associated protein 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ENPP1ectonucleotide pyrophosphatase/phosphodiesterase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GLAgalactosidase alpha | Mõnikord (5–29%) | Esineb 2 haiguses |
| HLA-DPA1major histocompatibility complex, class II, DP alpha 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HLA-DPB1major histocompatibility complex, class II, DP beta 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| IDUAalpha-L-iduronidase | Mõnikord (5–29%) | Esineb 1 haiguses |
| LCATlecithin-cholesterol acyltransferase | Mõnikord (5–29%) | Esineb 1 haiguses |
| PRTN3proteinase 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PTENphosphatase and tensin homolog | Mõnikord (5–29%) | Esineb 1 haiguses |
| PTPN22protein tyrosine phosphatase non-receptor type 22 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TRIM63tripartite motif containing 63 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TTRtransthyretin | Mõnikord (5–29%) | Esineb 1 haiguses |
| LMNAlamin A/C | Harva (1–4%) | Esineb 2 haiguses |
| PMM2phosphomannomutase 2 | Harva (1–4%) | Esineb 1 haiguses |
| ZMPSTE24zinc metallopeptidase STE24 | Harva (1–4%) | Esineb 1 haiguses |
| CYP27A1cytochrome P450 family 27 subfamily A member 1 | Pole registreeritud | Esineb 1 haiguses |
| XYLT1xylosyltransferase 1 | Pole registreeritud | Esineb 1 haiguses |
| XYLT2xylosyltransferase 2 | 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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Logi sisseKüsiSekveneeri oma genoom↗
From traits to your genome
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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Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
