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Požymis
Aneurysm
Klinikinis pavadinimas: Vascular dilatation
An abnormal increase in the diameter of an artery or vein, either as a diffuse dilatation or as a localized, sac-like outpouching of the vessel wall (aneurysm).
Santrauka
- Taip pat vadinama
- Aneurysmal disease, Aneurysms, Wider than typical opening or gap, Aneurysmal dilatation
- Kūno sistema
- Abnormality of the cardiovascular system
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Ši puslapis kaip duomenys
Norėdami perskaityti jį kaip JSON, pridėkite .json prie puslapio adreso arba nurodykite application/json.
library(jsonlite)
url <- "https://dantelabs.com/traits/vascular-dilatation.json"
page <- fromJSON(url)
page$trait$nameAneurysmHP:0002617
AtlasKam mes padedameMūsų mokslasProduktaiRezultatai
PrisijungtiKlaustiSekvenuokite savo genomą↗
Vienu tyrimu sužinokite genus, susijusius su Aneurysm, ir kitą jūsų genomo dalį.
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Įsigyti savo Genome Test52 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.
- Loeys-Dietz SyndromeReads 6 of these genesSMAD2SMAD3TGFB2TGFB3TGFBR1TGFBR2About this report →
- Polycystic Liver Disease (1 and 2)Reads 4 of these genesALG8LRP5PRKCSHSEC63About this report →
- Marfan Like SyndromesReads 6 of these genesSMAD2SMAD3TGFB2TGFB3TGFBR1TGFBR2About this report →
- Cutis LaxaReads 6 of these genesATP7ASLC2A10EFEMP2FBLN5LTBP1LTBP4About this report →
Show 48 more reports
- Aortic AneurysmReads 4 of these genesTGFB2TGFBR1TGFBR2ACTA2About this report →
- Hereditary Vascular MalformationsReads 2 of these genesEPHB4RASA1About this report →
- Ferguson-Smith Disease (Multiple Self-Healing Squamous Epithelioma)Reads 1 of these genesTGFBR1About this report →
- Johanson-Blizzard SyndromeReads 1 of these genesUBR1About this report →
- Microcephalic Osteodysplastic Primordial Dwarfism Type IIReads 1 of these genesPCNTAbout this report →
- OFD1-Related CiliopathyReads 1 of these genesOFD1About this report →
- PBX1-Related Kidney and Urinary Tract AnomaliesReads 1 of these genesPBX1About this report →
- Cerebral Arteriopathy with Subcortical Infarcts and LeukoencephalopathyReads 1 of these genesNOTCH3About this report →
- STAT1 and STAT3 Gain-of-Function DiseaseReads 1 of these genesSTAT3About this report →
- Noonan SyndromeReads 3 of these genesBRAFPTPN11RAF1About this report →
- Meckel SyndromeReads 2 of these genesMKS1TMEM67About this report →
- Disorder of Copper MetabolismReads 1 of these genesATP7AAbout this report →
- Carney Complex & Hereditary Adrenal Cushing SyndromeReads 1 of these genesPRKAR1AAbout this report →
- Moyamoya DiseaseReads 1 of these genesACTA2About this report →
- Pseudohypoparathyroidism & GNAS-Inactivation DisordersReads 1 of these genesPRKAR1AAbout this report →
- Joubert Syndrome And Related DisordersReads 3 of these genesOFD1MKS1TMEM67About this report →
- Nephronophthisis and Senior-Løken SyndromeReads 2 of these genesTMEM67WDR19About this report →
- Sclerosing Bone Dysplasias (High Bone Mass)Reads 1 of these genesLRP5About this report →
- Ehlers-Danlos SyndromeReads 2 of these genesPLOD1COL3A1About this report →
- Hypertrophic CardiomyopathyReads 3 of these genesBRAFPTPN11RAF1About this report →
- Ellis-van Creveld Syndrome and Cranioectodermal DysplasiaReads 1 of these genesWDR19About this report →
- Hyper-IgE SyndromeReads 1 of these genesSTAT3About this report →
- Waardenburg SyndromeReads 1 of these genesSOX10About this report →
- GlomerulosclerosisReads 1 of these genesCRB2About this report →
- Focal Segmental GlomerulosclerosisReads 1 of these genesCRB2About this report →
- Mendelian Susceptibility to Mycobacterial Disease (MSMD)Reads 1 of these genesIL12BAbout this report →
- Polycystic Kidney DiseaseReads 1 of these genesALG8About this report →
- LipodystrophyReads 1 of these genesCAVIN1About this report →
- OsteopetrosisReads 1 of these genesLRP5About this report →
- Zellweger Spectrum & Peroxisome Biogenesis DisordersReads 1 of these genesPEX12About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 2 of these genesMKS1TMEM67About this report →
- Primary Lymphoedema & Lymphatic MalformationsReads 1 of these genesEPHB4About this report →
- Charcot-Marie-Tooth DiseaseReads 2 of these genesATP7AFBLN5About this report →
- Neonatal Diabetes MellitusReads 1 of these genesMNX1About this report →
- Autoimmune DiseaseReads 1 of these genesSTAT3About this report →
- Bardet-Biedl and Alström SyndromesReads 1 of these genesMKS1About this report →
- Syndromic CraniosynostosisReads 1 of these genesWDR19About this report →
- Inherited Neurodegenerative DisordersReads 4 of these genesATP7AMKS1PEX12TMEM67About this report →
- Rare Hereditary Peripheral NeuropathiesReads 3 of these genesATP7AFBLN5PEX12About this report →
- VitreoretinopathyReads 1 of these genesLRP5About this report →
- Spinal Muscular AtrophyReads 1 of these genesATP7AAbout this report →
- Diabetes MellitusReads 1 of these genesMNX1About this report →
- Osteogenesis ImperfectaReads 1 of these genesLRP5About this report →
- Dilated CardiomyopathyReads 1 of these genesRAF1About this report →
- Other Inherited LeukodystrophiesReads 1 of these genesPEX12About this report →
- Retinitis PigmentosaReads 1 of these genesOFD1About this report →
- Congenital Disorders of GlycosylationReads 1 of these genesALG8About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesSTAT3About this report →
Vienu tyrimu sužinokite genus, susijusius su Aneurysm, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test46 genų susiję su Aneurysm
Šių genų pakitimai sukelia retas ligas, kuriose pasireiškia Aneurysm. 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 |
|---|---|---|
| NOTCH3notch receptor 3 | Visada | 1 ligoje |
| ATP7AATPase copper transporting alpha | Labai dažnai (80–99%) | 2 ligose |
| HLA-Bmajor histocompatibility complex, class I, B | Labai dažnai (80–99%) | 1 ligoje |
| IL12Binterleukin 12B | Labai dažnai (80–99%) | 1 ligoje |
| IPO8importin 8 | Labai dažnai (80–99%) | 1 ligoje |
| MLXMAX dimerization protein MLX | Labai dažnai (80–99%) | 1 ligoje |
| SLC2A10solute carrier family 2 member 10 | Labai dažnai (80–99%) | 1 ligoje |
| SMAD2SMAD family member 2 | Labai dažnai (80–99%) | 1 ligoje |
| SMAD3SMAD family member 3 | Labai dažnai (80–99%) | 2 ligose |
| TGFB2transforming growth factor beta 2 | Labai dažnai (80–99%) | 1 ligoje |
| TGFB3transforming growth factor beta 3 | Labai dažnai (80–99%) | 1 ligoje |
| TGFBR1transforming growth factor beta receptor 1 | Labai dažnai (80–99%) | 1 ligoje |
| TGFBR2transforming growth factor beta receptor 2 | Labai dažnai (80–99%) | 1 ligoje |
| EPHB4EPH receptor B4 | Dažnai (30–79%) | 1 ligoje |
| RASA1RAS p21 protein activator 1 | Dažnai (30–79%) | 1 ligoje |
| ALG8ALG8 alpha-1,3-glucosyltransferase | Kartais (5–29%) | 1 ligoje |
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Kartais (5–29%) | 1 ligoje |
| EFEMP2EGF-like fibulin extracellular matrix protein 2 | Kartais (5–29%) | 1 ligoje |
| FBLN5fibulin 5 | Kartais (5–29%) | 1 ligoje |
| LRP5LDL receptor related protein 5 | Kartais (5–29%) | 1 ligoje |
| LTBP1latent transforming growth factor beta binding protein 1 | Kartais (5–29%) | 1 ligoje |
| OFD1OFD1 centriole and centriolar satellite protein | Kartais (5–29%) | 2 ligose |
| PCNTpericentrin | Kartais (5–29%) | 1 ligoje |
| PLOD1procollagen-lysine,2-oxoglutarate 5-dioxygenase 1 | Kartais (5–29%) | 1 ligoje |
| PRKCSHPRKCSH beta subunit of glucosidase II | Kartais (5–29%) | 1 ligoje |
| PTPN11protein tyrosine phosphatase non-receptor type 11 | Kartais (5–29%) | 1 ligoje |
| RAF1Raf-1 proto-oncogene, serine/threonine kinase | Kartais (5–29%) | 1 ligoje |
| SEC63SEC63 protein translocation regulator | Kartais (5–29%) | 1 ligoje |
| STAT3signal transducer and activator of transcription 3 | Kartais (5–29%) | 1 ligoje |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Retai (1–4 %) | 1 ligoje |
| ACTA2actin alpha 2, smooth muscle | Neužfiksuota | 1 ligoje |
| CAVIN1caveolae associated protein 1 | Neužfiksuota | 1 ligoje |
| COL3A1collagen type III alpha 1 chain | Neužfiksuota | 1 ligoje |
| CRB2crumbs cell polarity complex component 2 | Neužfiksuota | 1 ligoje |
| LTBP4latent transforming growth factor beta binding protein 4 | Neužfiksuota | 1 ligoje |
| MKS1MKS transition zone complex subunit 1 | Neužfiksuota | 1 ligoje |
| MNX1motor neuron and pancreas homeobox 1 | Neužfiksuota | 1 ligoje |
| NPPAnatriuretic peptide A | Neužfiksuota | 1 ligoje |
| PAM16presequence translocase associated motor 16 | Neužfiksuota | 1 ligoje |
| PBX1PBX homeobox 1 | Neužfiksuota | 1 ligoje |
Rodyti dar 6 genų
| Genas | Kaip dažnai pasireiškia | Ligos |
|---|---|---|
| PEX12peroxisomal biogenesis factor 12 | Neužfiksuota | 1 ligoje |
| SALL4spalt like transcription factor 4 | Neužfiksuota | 1 ligoje |
| SOX10SRY-box transcription factor 10 | Neužfiksuota | 1 ligoje |
| TMEM67transmembrane protein 67 | Neužfiksuota | 1 ligoje |
| UBR1ubiquitin protein ligase E3 component n-recognin 1 | Neužfiksuota | 1 ligoje |
| WDR19WD repeat domain 19 | Neužfiksuota | 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 2026.10.19-9814e911.
AtlasKam mes padedameMūsų mokslasProduktaiRezultatai
PrisijungtiKlaustiSekvenuokite savo genomą↗
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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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