Cecha
Right ventricular hypertrophy
In this case the right ventricle is more muscular than normal, causing a characteristic boot-shaped (coeur-en-sabot) appearance as seen on anterior- posterior chest x-rays. Right ventricular hypertrophy is commonly associated with any form of right ventricular outflow obstruction or pulmonary hypertension, which may in turn owe its origin to left-sided disease. The echocardiographic signs are thickening of the anterior right ventricular wall and the septum. Cavity size is usually normal, or slightly enlarged. In many cases there is associated volume overload present due to tricuspid regurgitation, in the absence of this, septal motion is normal.
Podsumowanie
- Znana także jako
- Heart right ventricle hypertrophy
- Układ organizmu
- Abnormality of the cardiovascular system
Ta strona jako dane
Aby odczytać ją jako JSON, dodaj .json na końcu adresu strony lub zażądaj application/json.
library(jsonlite)
url <- "https://dantelabs.com/traits/right-ventricular-hypertrophy.json"
page <- fromJSON(url)
page$trait$nameOdczytaj geny powiązane z Right ventricular hypertrophy oraz resztę swojego genomu za pomocą jednego badania.
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Zamawiam Genome Test33 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.
- Kabuki SyndromeReads 2 of these genesKMT2DKDM6AAbout this report →
- Alveolar Capillary Dysplasia with Misalignment of Pulmonary VeinsReads 1 of these genesFOXF1About this report →
- ARC Syndrome 1 (VPS33B)Reads 1 of these genesVPS33BAbout this report →
- ARC Syndrome 2 (VIPAS39)Reads 1 of these genesVIPAS39About this report →
Show 29 more reports
- Simpson-Golabi-Behmel SyndromeReads 1 of these genesGPC3About this report →
- Distal MyopathiesReads 3 of these genesDYSFMYH7TTNAbout this report →
- Congenital MyopathiesReads 3 of these genesMYH7SELENONTTNAbout this report →
- Mucolipidoses (ML II, ML III and ML IV)Reads 1 of these genesGNPTABAbout this report →
- Limb-Girdle Muscular DystrophyReads 3 of these genesSGCGDYSFTTNAbout this report →
- GPI Anchor Biosynthesis DefectsReads 2 of these genesPIGAPIGNAbout this report →
- Dilated CardiomyopathyReads 3 of these genesSGCGMYH7TTNAbout this report →
- Adams-Oliver SyndromeReads 1 of these genesNOTCH1About this report →
- Heritable Pulmonary Arterial Hypertension (HPAH)Reads 1 of these genesBMPR2About this report →
- Surfactant Metabolism DysfunctionReads 1 of these genesSFTPBAbout this report →
- Congenital Myasthenic SyndromeReads 2 of these genesCOL13A1COLQAbout this report →
- Left Ventricular NoncompactionReads 1 of these genesMYH7About this report →
- Leigh SyndromeReads 3 of these genesSCO2FBXL4GTPBP3About this report →
- Congenital Anomalies of the Kidney and Urinary TractReads 1 of these genesSOX17About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesNOTCH1About this report →
- Myofibrillar MyopathiesReads 1 of these genesTTNAbout this report →
- Primary Mitochondrial DiseaseReads 3 of these genesSCO2FBXL4GTPBP3About this report →
- Hypertrophic CardiomyopathyReads 2 of these genesALPK3MYH7About this report →
- Cutis LaxaReads 1 of these genesLTBP4About this report →
- Nephronophthisis and Senior-Løken SyndromeReads 1 of these genesNPHP3About this report →
- Congenital Disorders of GlycosylationReads 2 of these genesPIGAPIGNAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 3 of these genesSCO2FBXL4GTPBP3About this report →
- Congenital Muscular DystrophiesReads 1 of these genesSELENONAbout this report →
- Nephrotic SyndromeReads 1 of these genesLAMB2About this report →
- Epilepsy (Full Panel)Reads 2 of these genesPIGASLC25A12About this report →
- Hypogonadotropic HypogonadismReads 1 of these genesPLXND1About this report →
- Lysosomal Storage DiseaseReads 1 of these genesGNPTABAbout this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesSCO2About this report →
- Intellectual DisabilityReads 1 of these genesNONOAbout this report →
Odczytaj geny powiązane z Right ventricular hypertrophy oraz resztę swojego genomu za pomocą jednego badania.
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Zamawiam Genome Test33 genów powiązanych z Right ventricular hypertrophy
Zmiany w tych genach powodują rzadkie choroby, w których występuje Right ventricular hypertrophy. Większość osób z tą cechą nie ma żadnej z tych chorób, a gen z tej listy nic nie mówi o czyimkolwiek własnym genomie.
| Gen | Jak często występuje | Choroby |
|---|---|---|
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Zawsze | W 1 chorobie |
| SOX17SRY-box transcription factor 17 | Zawsze | W 1 chorobie |
| ALPK3alpha kinase 3 | Bardzo często (80–99%) | W 1 chorobie |
| BMPR2bone morphogenetic protein receptor type 2 | Bardzo często (80–99%) | W 1 chorobie |
| CAPNS1calpain small subunit 1 | Często (30–79%) | W 1 chorobie |
| NONOnon-POU domain containing octamer binding | Często (30–79%) | W 2 chorobach |
| PLXND1plexin D1 | Często (30–79%) | W 1 chorobie |
| SCO2synthesis of cytochrome C oxidase 2 | Często (30–79%) | W 1 chorobie |
| SGCGsarcoglycan gamma | Często (30–79%) | W 1 chorobie |
| SLC25A12solute carrier family 25 member 12 | Często (30–79%) | W 1 chorobie |
| DYSFdysferlin | Czasami (5–29%) | W 1 chorobie |
| FBXL4F-box and leucine rich repeat protein 4 | Czasami (5–29%) | W 1 chorobie |
| FOXF1forkhead box F1 | Czasami (5–29%) | W 1 chorobie |
| GNPTABN-acetylglucosamine-1-phosphate transferase subunits alpha and beta | Czasami (5–29%) | W 1 chorobie |
| GPC3glypican 3 | Czasami (5–29%) | W 1 chorobie |
| GTPBP3GTP binding protein 3, mitochondrial | Czasami (5–29%) | W 1 chorobie |
| IPO8importin 8 | Czasami (5–29%) | W 1 chorobie |
| KMT2Dlysine methyltransferase 2D | Czasami (5–29%) | W 2 chorobach |
| LTBP4latent transforming growth factor beta binding protein 4 | Czasami (5–29%) | W 1 chorobie |
| MYH7myosin heavy chain 7 | Czasami (5–29%) | W 1 chorobie |
| NPHP3nephrocystin 3 | Czasami (5–29%) | W 1 chorobie |
| PIGNphosphatidylinositol glycan anchor biosynthesis class N | Czasami (5–29%) | W 1 chorobie |
| SELENONselenoprotein N | Czasami (5–29%) | W 1 chorobie |
| SFTPBsurfactant protein B | Czasami (5–29%) | W 1 chorobie |
| TTNtitin | Czasami (5–29%) | W 1 chorobie |
| COL13A1collagen type XIII alpha 1 chain | Rzadko (1–4%) | W 1 chorobie |
| COLQcollagen like tail subunit of asymmetric acetylcholinesterase | Rzadko (1–4%) | W 1 chorobie |
| KDM6Alysine demethylase 6A | Rzadko (1–4%) | W 1 chorobie |
| LAMB2laminin subunit beta 2 | Rzadko (1–4%) | W 1 chorobie |
| NOTCH1notch receptor 1 | Nie odnotowano | W 1 chorobie |
| STAMBPSTAM binding protein | Nie odnotowano | W 1 chorobie |
| VIPAS39VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog | Nie odnotowano | W 1 chorobie |
| VPS33BVPS33B late endosome and lysosome associated | Nie odnotowano | W 1 chorobie |
Jak często występuje wśród osób z jedną z chorób związanych z tym genem, najczęściej spośród wszystkich, według danych Human Phenotype Ontology. Te strony opisują cechy i badania, na których się opierają; nie są diagnozą, a w sprawie objawów należy zwrócić się do lekarza lub doradcy genetycznego.
Cechy nadrzędne
Skąd pochodzą te dane
- Human Phenotype Ontology, wydanie 2026-09-01: cecha, jej nazwy, definicja oraz geny z nią powiązane. Więcej informacji znajdą Państwo na stronie hpo.jax.org.
- Wydanie danych 2026.10.19-9814e911.
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