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Raynaud phenomenon
Resumé
- Også kaldet
- Raynaud's phenomenon
- Kropssystem
- Abnormality of the cardiovascular system
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Denne side som data
Tilføj .json til sidens adresse, eller bed om application/json, for at læse den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/raynaud-phenomenon.json"
page <- fromJSON(url)
page$trait$nameRaynaud phenomenonHP:0030880
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Læs de gener, der er knyttet til Raynaud phenomenon, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test39 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.
- Aicardi-Goutieres SyndromeReads 8 of these genesTREX1ADARIFIH1RNASEH2ARNASEH2BRNASEH2CAbout this report →
- Rare Monogenic Autoinflammatory DiseasesReads 12 of these genesSTING1TREX1ADA2TNFAIP3ACP5ADARAbout this report →
- Type I InterferonopathiesReads 4 of these genesSTING1TREX1ACP5IFIH1About this report →
- Moyamoya DiseaseReads 2 of these genesGUCY1A1SAMHD1About this report →
Show 35 more reports
- COL4A1-Related DisorderReads 1 of these genesCOL4A1About this report →
- Deficiency of Adenosine Deaminase 2 (DADA2)Reads 1 of these genesADA2About this report →
- Dyschromatosis Symmetrica HereditariaReads 1 of these genesADARAbout this report →
- Gitelman SyndromeReads 1 of these genesSLC12A3About this report →
- Restrictive Dermopathy (ZMPSTE24)Reads 1 of these genesZMPSTE24About this report →
- Rett Syndrome and MECP2-Related DisordersReads 1 of these genesMECP2About this report →
- Other Inborn Errors of ImmunityReads 14 of these genesTREX1C4AC4BCR2CTLA4IL10About this report →
- Other Inherited LeukodystrophiesReads 8 of these genesTREX1ADARIFIH1RNASEH2ARNASEH2BRNASEH2CAbout this report →
- Systemic Lupus ErythematosusReads 2 of these genesTREX1SAT1About this report →
- Cerebral Arteriopathy with Subcortical Infarcts and LeukoencephalopathyReads 1 of these genesNOTCH3About this report →
- Autoimmune DiseaseReads 3 of these genesTREX1CTLA4SAT1About this report →
- Common Variable Immunodeficiency (Monogenic CVID)Reads 2 of these genesCR2SEC61A1About this report →
- LipodystrophyReads 2 of these genesLMNAZMPSTE24About this report →
- Primary HyperoxaluriaReads 1 of these genesAGXTAbout this report →
- Inherited Complement and Properdin DeficienciesReads 2 of these genesC4AC4BAbout this report →
- Autosomal Dominant Tubulointerstitial Kidney DiseaseReads 1 of these genesSEC61A1About this report →
- Bartter DiseaseReads 1 of these genesCLCNKBAbout this report →
- Periventricular Nodular HeterotopiaReads 1 of these genesFLNAAbout this report →
- Inherited Neurodegenerative DisordersReads 8 of these genesTREX1ADARIFIH1RNASEH2ARNASEH2BRNASEH2CAbout this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 1 of these genesFLNAAbout this report →
- Inflammatory Bowel Diseases (IBD)Reads 1 of these genesIL10About this report →
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 1 of these genesCTLA4About this report →
- IPEX Syndrome and Other TregopathiesReads 1 of these genesCTLA4About this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesLMNAAbout this report →
- Inherited Congenital Heart DefectsReads 1 of these genesFLNAAbout this report →
- Noonan SyndromeReads 1 of these genesHRASAbout this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesLMNAAbout this report →
- Osteogenesis ImperfectaReads 1 of these genesIFIH1About this report →
- Epilepsy (Full Panel)Reads 2 of these genesFLNAMECP2About this report →
- Dilated CardiomyopathyReads 1 of these genesLMNAAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 2 of these genesCOQ2LMNAAbout this report →
- Hypertrophic CardiomyopathyReads 1 of these genesHRASAbout this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesLMNAAbout this report →
- Primary Mitochondrial DiseaseReads 1 of these genesCOQ2About this report →
- Intellectual DisabilityReads 1 of these genesMECP2About this report →
Læs de gener, der er knyttet til Raynaud phenomenon, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test60 gener knyttet til Raynaud phenomenon
Ændringer i disse gener forårsager sjældne tilstande, hvor Raynaud phenomenon ses. De fleste med dette træk har ingen af disse tilstande, og et gen på denne liste siger intet om nogens eget genom.
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| FEM1Bfem-1 homolog B | Altid | I 1 tilstand |
| FLNAfilamin A | Altid | I 1 tilstand |
| LBRlamin B receptor | Altid | I 1 tilstand |
| STING1stimulator of interferon response cGAMP interactor 1 | Altid | I 1 tilstand |
| TREX1three prime repair exonuclease 1 | Meget ofte (80–99 %) | I 5 tilstande |
| ADA2adenosine deaminase 2 | Ofte (30–79 %) | I 2 tilstande |
| APOLD1apolipoprotein L domain containing 1 | Ofte (30–79 %) | I 1 tilstand |
| BANK1B cell scaffold protein with ankyrin repeats 1 | Ofte (30–79 %) | I 1 tilstand |
| BLKBLK proto-oncogene, Src family tyrosine kinase | Ofte (30–79 %) | I 1 tilstand |
| C4Acomplement C4A (Chido/Rodgers blood group) | Ofte (30–79 %) | I 1 tilstand |
| C4Bcomplement C4B (Chido/Rodgers blood group) | Ofte (30–79 %) | I 1 tilstand |
| COL4A1collagen type IV alpha 1 chain | Ofte (30–79 %) | I 2 tilstande |
| COQ2coenzyme Q2, polyprenyltransferase | Ofte (30–79 %) | I 2 tilstande |
| CR2complement C3d receptor 2 | Ofte (30–79 %) | I 1 tilstand |
| CTLA4cytotoxic T-lymphocyte associated protein 4 | Ofte (30–79 %) | I 1 tilstand |
| DNASE1deoxyribonuclease 1 | Ofte (30–79 %) | I 2 tilstande |
| ETS1ETS proto-oncogene 1, transcription factor | Ofte (30–79 %) | I 1 tilstand |
| FCGR2BFc gamma receptor IIb | Ofte (30–79 %) | I 2 tilstande |
| FCGR3BFc gamma receptor IIIb | Ofte (30–79 %) | I 1 tilstand |
| FLT3LGfms related receptor tyrosine kinase 3 ligand | Ofte (30–79 %) | I 1 tilstand |
| GUCY1A1guanylate cyclase 1 soluble subunit alpha 1 | Ofte (30–79 %) | I 2 tilstande |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Ofte (30–79 %) | I 1 tilstand |
| IGHG1immunoglobulin heavy constant gamma 1 (G1m marker) | Ofte (30–79 %) | I 1 tilstand |
| IL10interleukin 10 | Ofte (30–79 %) | I 1 tilstand |
| IRAK1interleukin 1 receptor associated kinase 1 | Ofte (30–79 %) | I 2 tilstande |
| IRF5interferon regulatory factor 5 | Ofte (30–79 %) | I 1 tilstand |
| ITGAMintegrin subunit alpha M | Ofte (30–79 %) | I 1 tilstand |
| JAZF1JAZF zinc finger 1 | Ofte (30–79 %) | I 1 tilstand |
| KIAA0319LKIAA0319 like | Ofte (30–79 %) | I 1 tilstand |
| MECP2methyl-CpG binding protein 2 | Ofte (30–79 %) | I 1 tilstand |
| PDCD1programmed cell death 1 | Ofte (30–79 %) | I 1 tilstand |
| PTPN22protein tyrosine phosphatase non-receptor type 22 | Ofte (30–79 %) | I 1 tilstand |
| PXKPX domain containing serine/threonine kinase like | Ofte (30–79 %) | I 1 tilstand |
| RNF125ring finger protein 125 | Ofte (30–79 %) | I 1 tilstand |
| SPP1secreted phosphoprotein 1 | Ofte (30–79 %) | I 2 tilstande |
| STAT4signal transducer and activator of transcription 4 | Ofte (30–79 %) | I 2 tilstande |
| TLR7toll like receptor 7 | Ofte (30–79 %) | I 2 tilstande |
| TNFAIP3TNF alpha induced protein 3 | Ofte (30–79 %) | I 1 tilstand |
| TNFSF4TNF superfamily member 4 | Ofte (30–79 %) | I 1 tilstand |
| TNIP1TNFAIP3 interacting protein 1 | Ofte (30–79 %) | I 1 tilstand |
Vis 20 gener mere
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| UBE2L3ubiquitin conjugating enzyme E2 L3 | Ofte (30–79 %) | I 1 tilstand |
| ACP5acid phosphatase 5, tartrate resistant | Nogle gange (5–29 %) | I 2 tilstande |
| ADARadenosine deaminase RNA specific | Nogle gange (5–29 %) | I 1 tilstand |
| FCGR2AFc gamma receptor IIa | Nogle gange (5–29 %) | I 1 tilstand |
| IFIH1interferon induced with helicase C domain 1 | Nogle gange (5–29 %) | I 1 tilstand |
| LMNAlamin A/C | Nogle gange (5–29 %) | I 1 tilstand |
| LSM11LSM11, U7 small nuclear RNA associated | Nogle gange (5–29 %) | I 1 tilstand |
| NOTCH3notch receptor 3 | Nogle gange (5–29 %) | I 1 tilstand |
| RNASEH2Aribonuclease H2 subunit A | Nogle gange (5–29 %) | I 1 tilstand |
| RNASEH2Bribonuclease H2 subunit B | Nogle gange (5–29 %) | I 1 tilstand |
| RNASEH2Cribonuclease H2 subunit C | Nogle gange (5–29 %) | I 1 tilstand |
| RNU7-1RNA, U7 small nuclear 1 | Nogle gange (5–29 %) | I 1 tilstand |
| SAMHD1SAM and HD domain containing deoxynucleoside triphosphate triphosphohydrolase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| SEC61A1SEC61 translocon subunit alpha 1 | Nogle gange (5–29 %) | I 1 tilstand |
| ZMPSTE24zinc metallopeptidase STE24 | Nogle gange (5–29 %) | I 1 tilstand |
| CLCNKBchloride voltage-gated channel Kb | Sjældent (1–4%) | I 1 tilstand |
| HRASHRas proto-oncogene, GTPase | Sjældent (1–4%) | I 1 tilstand |
| SAT1spermidine/spermine N1-acetyltransferase 1 | Sjældent (1–4%) | I 1 tilstand |
| SLC12A3solute carrier family 12 member 3 | Sjældent (1–4%) | I 1 tilstand |
| AGXTalanine--glyoxylate aminotransferase | Ikke registreret | I 1 tilstand |
Hvor hyppigt det ses hos personer med en af genets tilstande, den hyppigste værdi på tværs af dem, sådan som Human Phenotype Ontology registrerer det. Disse sider beskriver egenskaber og den forskning, der ligger bag dem. De er ikke en diagnose, og hvis du har spørgsmål om symptomer, bør du spørge en læge eller genetisk rådgiver.
Bredere træk
Hvor oplysningerne kommer fra
- Human Phenotype Ontology, udgivelse 2026-09-01: egenskaben, dens navne, definition og de gener, der er knyttet til den. Læs mere på hpo.jax.org.
- Dataudgivelse 2026.10.21-777c9289.
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