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형질
Fluid accumulation in lower limbs
임상 명칭: 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.
요약
- 다른 명칭
- 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
Atlas우리가 돕는 분들과학적 근거제품연구 성과
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library(jsonlite)
url <- "https://dantelabs.com/traits/pedal-edema.json"
page <- fromJSON(url)
page$trait$nameFluid accumulation in lower limbsHP:0010741
Atlas우리가 돕는 분들과학적 근거제품연구 성과
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Fluid accumulation in lower limbs과(와) 연결된 유전자와 나머지 게놈을 한 번의 검사로 확인하세요.
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내 Genome Test 받기61 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 →
Fluid accumulation in lower limbs과(와) 연결된 유전자와 나머지 게놈을 한 번의 검사로 확인하세요.
$449부터배송비 무료 · 결과는 6~8주 내 제공
내 Genome Test 받기연관 유전자 53개: Fluid accumulation in lower limbs
이 유전자들의 변화는 Fluid accumulation in lower limbs 증상이 나타나는 희귀 질환을 일으킵니다. 이 형질을 가진 대부분의 사람에게는 이러한 질환이 없으며, 이 목록에 있는 유전자가 누구의 개인 유전체에 대해서도 말해 주는 것은 없습니다.
| 유전자 | 나타나는 빈도 | 질환 |
|---|---|---|
| ATP7BATPase copper transporting beta | 항상 | 질환 1개에서 나타남 |
| FIBPFGF1 intracellular binding protein | 항상 | 질환 1개에서 나타남 |
| PLD4phospholipase D family member 4 | 항상 | 질환 1개에서 나타남 |
| TIE1tyrosine kinase with immunoglobulin like and EGF like domains 1 | 항상 | 질환 1개에서 나타남 |
| FN1fibronectin 1 | 매우 자주 (80–99%) | 질환 1개에서 나타남 |
| ALBalbumin | 자주 (30–79%) | 질환 1개에서 나타남 |
| EIF2AK4eukaryotic translation initiation factor 2 alpha kinase 4 | 자주 (30–79%) | 질환 1개에서 나타남 |
| EPHB4EPH receptor B4 | 자주 (30–79%) | 질환 1개에서 나타남 |
| FLT4fms related receptor tyrosine kinase 4 | 자주 (30–79%) | 질환 1개에서 나타남 |
| GJC2gap junction protein gamma 2 | 자주 (30–79%) | 질환 1개에서 나타남 |
| VEGFCvascular endothelial growth factor C | 자주 (30–79%) | 질환 1개에서 나타남 |
| ZNHIT3zinc finger HIT-type containing 3 | 자주 (30–79%) | 질환 1개에서 나타남 |
| ACTC1actin alpha cardiac muscle 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| ALG8ALG8 alpha-1,3-glucosyltransferase | 가끔 (5–29%) | 질환 1개에서 나타남 |
| AP1S3adaptor related protein complex 1 subunit sigma 3 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| APC2APC regulator of Wnt signaling pathway 2 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| CD4CD4 molecule | 가끔 (5–29%) | 질환 1개에서 나타남 |
| CITED2Cbp/p300 interacting transactivator with ED-rich tail 2 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| GATA4GATA binding protein 4 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| GATA6GATA binding protein 6 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| IKBKGinhibitor of nuclear factor kappa B kinase regulatory subunit gamma | 가끔 (5–29%) | 질환 1개에서 나타남 |
| IL36RNinterleukin 36 receptor antagonist | 가끔 (5–29%) | 질환 1개에서 나타남 |
| IRF4interferon regulatory factor 4 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| LRP5LDL receptor related protein 5 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| MAGEL2MAGE family member L2 | 가끔 (5–29%) | 질환 3개에서 나타남 |
| MEFVMEFV innate immunity regulator, pyrin | 가끔 (5–29%) | 질환 1개에서 나타남 |
| MYD88MYD88 innate immune signal transduction adaptor | 가끔 (5–29%) | 질환 1개에서 나타남 |
| MYH6myosin heavy chain 6 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| MYH7myosin heavy chain 7 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| NDNnecdin, MAGE family member | 가끔 (5–29%) | 질환 3개에서 나타남 |
| NFKBIANFKB inhibitor alpha | 가끔 (5–29%) | 질환 1개에서 나타남 |
| NKX2-5NK2 homeobox 5 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| NSD1nuclear receptor binding SET domain protein 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| OCA2OCA2 melanosomal transmembrane protein | 가끔 (5–29%) | 질환 3개에서 나타남 |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | 가끔 (5–29%) | 질환 1개에서 나타남 |
| PRKCSHPRKCSH beta subunit of glucosidase II | 가끔 (5–29%) | 질환 1개에서 나타남 |
| SCN10Asodium voltage-gated channel alpha subunit 10 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| SCN11Asodium voltage-gated channel alpha subunit 11 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| SCN9Asodium voltage-gated channel alpha subunit 9 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| SEC63SEC63 protein translocation regulator | 가끔 (5–29%) | 질환 1개에서 나타남 |
유전자 13개 더 보기
| 유전자 | 나타나는 빈도 | 질환 |
|---|---|---|
| SNRPNsmall nuclear ribonucleoprotein polypeptide N | 가끔 (5–29%) | 질환 3개에서 나타남 |
| TBX20T-box transcription factor 20 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| TLL1tolloid like 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| TNXBtenascin XB | 가끔 (5–29%) | 질환 1개에서 나타남 |
| TRAF7TNF receptor associated factor 7 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| ATRXATRX chromatin remodeler | 드물게 (1–4%) | 질환 1개에서 나타남 |
| BRAFB-Raf proto-oncogene, serine/threonine kinase | 드물게 (1–4%) | 질환 1개에서 나타남 |
| CDH23cadherin related 23 | 드물게 (1–4%) | 질환 1개에서 나타남 |
| NR3C1nuclear receptor subfamily 3 group C member 1 | 드물게 (1–4%) | 질환 1개에서 나타남 |
| TP53tumor protein p53 | 드물게 (1–4%) | 질환 1개에서 나타남 |
| USP48ubiquitin specific peptidase 48 | 드물게 (1–4%) | 질환 1개에서 나타남 |
| USP8ubiquitin specific peptidase 8 | 드물게 (1–4%) | 질환 1개에서 나타남 |
| MKKSMKKS centrosomal shuttling protein | 기록되지 않음 | 질환 1개에서 나타남 |
Human Phenotype Ontology가 기록한, 해당 유전자와 관련된 질환을 가진 사람들 가운데 이 특징이 나타나는 빈도입니다. 이 페이지는 특징과 그 바탕이 되는 연구를 설명하며, 진단이 아닙니다. 증상에 대해서는 의사나 유전 상담사에게 문의하시기 바랍니다.
하위 형질
상위 형질
출처
- Human Phenotype Ontology, 버전 2026-09-01: 특징, 명칭, 정의 및 이와 연결된 유전자입니다. 자세한 내용은 hpo.jax.org에서 확인하실 수 있습니다.
- 데이터 버전 2026.10.19-9814e911.
Atlas우리가 돕는 분들과학적 근거제품연구 성과
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