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Cecha
Fluid accumulation in lower limbs
Nazwa kliniczna: Pedal edema
An abnormal accumulation of excess fluid in the lower extremity resulting in swelling of the feet and extending upward to the lower leg.
Podsumowanie
- Znana także jako
- Lower leg swelling, Edema of the lower limbs, Leg edema, Leg oedema, Oedema of the lower limbs, Pedal oedema, Peripheral edema of lower extremity, Peripheral oedema of lower extremity
- Układ organizmu
- Abnormality of limbsLaboratory abnormality
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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/pedal-edema.json"
page <- fromJSON(url)
page$trait$nameFluid accumulation in lower limbsHP:0010741
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Odczytaj geny powiązane z Fluid accumulation in lower limbs oraz resztę swojego genomu za pomocą jednego badania.
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Zamawiam Genome Test61 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.
- Polycystic Liver Disease (1 and 2)Reads 4 of these genesALG8LRP5PRKCSHSEC63About this report →
- Inherited Congenital Heart DefectsReads 7 of these genesACTC1GATA4GATA6MYH6NKX2-5TBX20About this report →
- Primary Lymphoedema & Lymphatic MalformationsReads 5 of these genesTIE1EPHB4FLT4GJC2VEGFCAbout this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 3 of these genesMAGEL2NSD1SNRPNAbout this report →
Show 57 more reports
- Congenital AnalbuminaemiaReads 1 of these genesALBAbout this report →
- Familial Mediterranean FeverReads 1 of these genesMEFVAbout this report →
- FLT4-Related Congenital Heart DiseaseReads 1 of these genesFLT4About this report →
- Li-Fraumeni SyndromeReads 1 of these genesTP53About this report →
- Wilson DiseaseReads 1 of these genesATP7BAbout this report →
- X-linked Autoinflammatory DiseaseReads 1 of these genesIKBKGAbout this report →
- Left Ventricular NoncompactionReads 2 of these genesACTC1MYH7About this report →
- Hypertrophic CardiomyopathyReads 5 of these genesACTC1MYH6MYH7NSD1BRAFAbout this report →
- Disorder of Copper MetabolismReads 1 of these genesATP7BAbout this report →
- HyperthyroidismReads 1 of these genesALBAbout this report →
- Tetralogy of FallotReads 1 of these genesNKX2-5About this report →
- Carney Complex & Hereditary Adrenal Cushing SyndromeReads 1 of these genesPRKAR1AAbout this report →
- Hereditary Vascular MalformationsReads 1 of these genesEPHB4About this report →
- Overgrowth Syndromes (Sotos, Weaver, Tatton-Brown-Rahman, Malan)Reads 1 of these genesNSD1About this report →
- Pseudohypoparathyroidism & GNAS-Inactivation DisordersReads 1 of these genesPRKAR1AAbout this report →
- Ectodermal DysplasiasReads 2 of these genesIKBKGNFKBIAAbout this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 2 of these genesGATA4ATRXAbout this report →
- Neonatal Diabetes MellitusReads 2 of these genesGATA4GATA6About this report →
- Sclerosing Bone Dysplasias (High Bone Mass)Reads 1 of these genesLRP5About this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 2 of these genesSCN11ASCN9AAbout this report →
- Dilated CardiomyopathyReads 3 of these genesACTC1MYH7TBX20About this report →
- Heritable Pulmonary Arterial Hypertension (HPAH)Reads 1 of these genesEIF2AK4About this report →
- Syndromic and Metabolic CardiomyopathiesReads 1 of these genesNKX2-5About this report →
- VitreoretinopathyReads 2 of these genesIKBKGLRP5About this report →
- Diabetes MellitusReads 2 of these genesGATA4GATA6About this report →
- Thyroid CancerReads 2 of these genesALBNKX2-5About this report →
- Familial Glucocorticoid DeficiencyReads 1 of these genesNR3C1About this report →
- Malignant Endocrine NeoplasmReads 1 of these genesTP53About this report →
- Oculocutaneous AlbinismReads 1 of these genesOCA2About this report →
- Epiphyseal and Spondyloepiphyseal DysplasiasReads 1 of these genesFN1About this report →
- Kidney CancerReads 1 of these genesTP53About this report →
- Polycystic Kidney DiseaseReads 1 of these genesALG8About this report →
- Usher SyndromeReads 1 of these genesCDH23About this report →
- Urinary and Renal System TumourReads 1 of these genesTP53About this report →
- Hypogonadotropic HypogonadismReads 2 of these genesMAGEL2SNRPNAbout this report →
- Other Inborn Errors of ImmunityReads 4 of these genesIKBKGIRF4MYD88NFKBIAAbout this report →
- OsteopetrosisReads 1 of these genesLRP5About this report →
- Complex Cortical Dysplasia and Frontoparietal PolymicrogyriaReads 1 of these genesAPC2About this report →
- Distal MyopathiesReads 1 of these genesMYH7About this report →
- Congenital HypothyroidismReads 1 of these genesNKX2-5About this report →
- Congenital MyopathiesReads 1 of these genesMYH7About this report →
- Ehlers-Danlos SyndromeReads 1 of these genesTNXBAbout this report →
- Noonan SyndromeReads 1 of these genesBRAFAbout this report →
- Bardet-Biedl and Alström SyndromesReads 1 of these genesMKKSAbout this report →
- Lissencephaly Spectrum DisordersReads 1 of these genesAPC2About this report →
- Syndromic Complex Neurodevelopmental DisorderReads 1 of these genesTRAF7About this report →
- Hearing Loss and DeafnessReads 2 of these genesCDH23USP48About this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 1 of these genesGJC2About this report →
- Rare Hereditary Peripheral NeuropathiesReads 3 of these genesSCN10ASCN11ASCN9AAbout this report →
- Osteogenesis ImperfectaReads 1 of these genesLRP5About this report →
- Rare Monogenic Autoinflammatory DiseasesReads 1 of these genesIL36RNAbout this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesGJC2About this report →
- Other Inherited LeukodystrophiesReads 1 of these genesGJC2About this report →
- Inherited Neurodegenerative DisordersReads 2 of these genesGJC2ZNHIT3About this report →
- Congenital Disorders of GlycosylationReads 1 of these genesALG8About this report →
- Epilepsy (Full Panel)Reads 1 of these genesSCN9AAbout this report →
- Intellectual DisabilityReads 1 of these genesATRXAbout this report →
Odczytaj geny powiązane z Fluid accumulation in lower limbs oraz resztę swojego genomu za pomocą jednego badania.
Od 449 $Bezpłatna wysyłka · Wyniki w ciągu 6–8 tygodni
Zamawiam Genome Test53 genów powiązanych z Fluid accumulation in lower limbs
Zmiany w tych genach powodują rzadkie choroby, w których występuje Fluid accumulation in lower limbs. 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 |
|---|---|---|
| ATP7BATPase copper transporting beta | Zawsze | W 1 chorobie |
| FIBPFGF1 intracellular binding protein | Zawsze | W 1 chorobie |
| PLD4phospholipase D family member 4 | Zawsze | W 1 chorobie |
| TIE1tyrosine kinase with immunoglobulin like and EGF like domains 1 | Zawsze | W 1 chorobie |
| FN1fibronectin 1 | Bardzo często (80–99%) | W 1 chorobie |
| ALBalbumin | Często (30–79%) | W 1 chorobie |
| EIF2AK4eukaryotic translation initiation factor 2 alpha kinase 4 | Często (30–79%) | W 1 chorobie |
| EPHB4EPH receptor B4 | Często (30–79%) | W 1 chorobie |
| FLT4fms related receptor tyrosine kinase 4 | Często (30–79%) | W 1 chorobie |
| GJC2gap junction protein gamma 2 | Często (30–79%) | W 1 chorobie |
| VEGFCvascular endothelial growth factor C | Często (30–79%) | W 1 chorobie |
| ZNHIT3zinc finger HIT-type containing 3 | Często (30–79%) | W 1 chorobie |
| ACTC1actin alpha cardiac muscle 1 | Czasami (5–29%) | W 1 chorobie |
| ALG8ALG8 alpha-1,3-glucosyltransferase | Czasami (5–29%) | W 1 chorobie |
| AP1S3adaptor related protein complex 1 subunit sigma 3 | Czasami (5–29%) | W 1 chorobie |
| APC2APC regulator of Wnt signaling pathway 2 | Czasami (5–29%) | W 1 chorobie |
| CD4CD4 molecule | Czasami (5–29%) | W 1 chorobie |
| CITED2Cbp/p300 interacting transactivator with ED-rich tail 2 | Czasami (5–29%) | W 1 chorobie |
| GATA4GATA binding protein 4 | Czasami (5–29%) | W 1 chorobie |
| GATA6GATA binding protein 6 | Czasami (5–29%) | W 1 chorobie |
| IKBKGinhibitor of nuclear factor kappa B kinase regulatory subunit gamma | Czasami (5–29%) | W 1 chorobie |
| IL36RNinterleukin 36 receptor antagonist | Czasami (5–29%) | W 1 chorobie |
| IRF4interferon regulatory factor 4 | Czasami (5–29%) | W 1 chorobie |
| LRP5LDL receptor related protein 5 | Czasami (5–29%) | W 1 chorobie |
| MAGEL2MAGE family member L2 | Czasami (5–29%) | W 3 chorobach |
| MEFVMEFV innate immunity regulator, pyrin | Czasami (5–29%) | W 1 chorobie |
| MYD88MYD88 innate immune signal transduction adaptor | Czasami (5–29%) | W 1 chorobie |
| MYH6myosin heavy chain 6 | Czasami (5–29%) | W 1 chorobie |
| MYH7myosin heavy chain 7 | Czasami (5–29%) | W 1 chorobie |
| NDNnecdin, MAGE family member | Czasami (5–29%) | W 3 chorobach |
| NFKBIANFKB inhibitor alpha | Czasami (5–29%) | W 1 chorobie |
| NKX2-5NK2 homeobox 5 | Czasami (5–29%) | W 1 chorobie |
| NSD1nuclear receptor binding SET domain protein 1 | Czasami (5–29%) | W 1 chorobie |
| OCA2OCA2 melanosomal transmembrane protein | Czasami (5–29%) | W 3 chorobach |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Czasami (5–29%) | W 1 chorobie |
| PRKCSHPRKCSH beta subunit of glucosidase II | Czasami (5–29%) | W 1 chorobie |
| SCN10Asodium voltage-gated channel alpha subunit 10 | Czasami (5–29%) | W 1 chorobie |
| SCN11Asodium voltage-gated channel alpha subunit 11 | Czasami (5–29%) | W 1 chorobie |
| SCN9Asodium voltage-gated channel alpha subunit 9 | Czasami (5–29%) | W 1 chorobie |
| SEC63SEC63 protein translocation regulator | Czasami (5–29%) | W 1 chorobie |
Pokaż jeszcze 13 genów
| Gen | Jak często występuje | Choroby |
|---|---|---|
| SNRPNsmall nuclear ribonucleoprotein polypeptide N | Czasami (5–29%) | W 3 chorobach |
| TBX20T-box transcription factor 20 | Czasami (5–29%) | W 1 chorobie |
| TLL1tolloid like 1 | Czasami (5–29%) | W 1 chorobie |
| TNXBtenascin XB | Czasami (5–29%) | W 1 chorobie |
| TRAF7TNF receptor associated factor 7 | Czasami (5–29%) | W 1 chorobie |
| ATRXATRX chromatin remodeler | Rzadko (1–4%) | W 1 chorobie |
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Rzadko (1–4%) | W 1 chorobie |
| CDH23cadherin related 23 | Rzadko (1–4%) | W 1 chorobie |
| NR3C1nuclear receptor subfamily 3 group C member 1 | Rzadko (1–4%) | W 1 chorobie |
| TP53tumor protein p53 | Rzadko (1–4%) | W 1 chorobie |
| USP48ubiquitin specific peptidase 48 | Rzadko (1–4%) | W 1 chorobie |
| USP8ubiquitin specific peptidase 8 | Rzadko (1–4%) | W 1 chorobie |
| MKKSMKKS centrosomal shuttling protein | 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 podrzędne
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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