AtlasTræk
Lower limb pain
An unpleasant sensation characterized by physical discomfort (such as pricking, throbbing, or aching) localized to the leg.
Resumé
- Også kaldet
- Leg pain
AtlasDenne 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/lower-limb-pain.json"
page <- fromJSON(url)
page$trait$nameLæs de gener, der er knyttet til Lower limb pain, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test21 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.
- Cerebral Arteriopathy with Subcortical Infarcts and LeukoencephalopathyReads 1 of these genesHTRA1About this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 4 of these genesKRT16KRT17KRT6AKRT6BAbout this report →
- Familial Periodic ParalysisReads 1 of these genesSCN4AAbout this report →
- Hereditary Vascular MalformationsReads 1 of these genesRASA1About this report →
Show 17 more reports
- Mucopolysaccharidosis Type III (Sanfilippo Syndrome)Reads 1 of these genesNAGLUAbout this report →
- Sclerosing Bone Dysplasias (High Bone Mass)Reads 1 of these genesTGFB1About this report →
- Hereditary Periodic Fever SyndromesReads 1 of these genesNLRP12About this report →
- Inflammatory Bowel Diseases (IBD)Reads 1 of these genesTGFB1About this report →
- Loeys-Dietz SyndromeReads 1 of these genesTGFB2About this report →
- Hereditary Spastic ParaplegiaReads 3 of these genesALDH18A1ERLIN1SPG7About this report →
- Leigh SyndromeReads 3 of these genesSCO2MT-ATP6MT-TKAbout this report →
- Charcot-Marie-Tooth DiseaseReads 3 of these genesNAGLUSCO2MMEAbout this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 2 of these genesSCN4APRKRAAbout this report →
- Marfan Like SyndromesReads 1 of these genesTGFB2About this report →
- Type I InterferonopathiesReads 1 of these genesACP5About this report →
- Aortic AneurysmReads 1 of these genesTGFB2About this report →
- Cutis LaxaReads 1 of these genesALDH18A1About this report →
- Congenital Myasthenic SyndromeReads 1 of these genesSCN4AAbout this report →
- Rare Monogenic Autoinflammatory DiseasesReads 1 of these genesACP5About this report →
- Lysosomal Storage DiseaseReads 1 of these genesNAGLUAbout this report →
- Primary Mitochondrial DiseaseReads 1 of these genesSCO2About this report →
Læs de gener, der er knyttet til Lower limb pain, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test22 gener knyttet til Lower limb pain
Ændringer i disse gener forårsager sjældne tilstande, hvor Lower limb pain 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 |
|---|---|---|
| FDXRferredoxin reductase | Altid | I 1 tilstand |
| HEPHL1hephaestin like 1 | Altid | I 1 tilstand |
| NAGLUN-acetyl-alpha-glucosaminidase | Altid | I 1 tilstand |
| SCN4Asodium voltage-gated channel alpha subunit 4 | Altid | I 1 tilstand |
| SCO2synthesis of cytochrome C oxidase 2 | Altid | I 1 tilstand |
| TGFB1transforming growth factor beta 1 | Altid | I 1 tilstand |
| KRT16keratin 16 | Meget ofte (80–99 %) | I 1 tilstand |
| KRT17keratin 17 | Meget ofte (80–99 %) | I 1 tilstand |
| KRT6Akeratin 6A | Meget ofte (80–99 %) | I 1 tilstand |
| KRT6Bkeratin 6B | Meget ofte (80–99 %) | I 1 tilstand |
| MT-ATP6mitochondrially encoded ATP synthase membrane subunit 6 | Meget ofte (80–99 %) | I 1 tilstand |
| HTRA1HtrA serine peptidase 1 | Ofte (30–79 %) | I 1 tilstand |
| MT-TKmitochondrially encoded tRNA-Lys (AAA/G) | Ofte (30–79 %) | I 1 tilstand |
| NLRP12NLR family pyrin domain containing 12 | Ofte (30–79 %) | I 1 tilstand |
| PRKRAprotein activator of interferon induced protein kinase EIF2AK2 | Ofte (30–79 %) | I 2 tilstande |
| ACP5acid phosphatase 5, tartrate resistant | Nogle gange (5–29 %) | I 1 tilstand |
| ALDH18A1aldehyde dehydrogenase 18 family member A1 | Nogle gange (5–29 %) | I 1 tilstand |
| ERLIN1ER lipid raft associated 1 | Nogle gange (5–29 %) | I 1 tilstand |
| MMEmembrane metalloendopeptidase | Nogle gange (5–29 %) | I 1 tilstand |
| RASA1RAS p21 protein activator 1 | Nogle gange (5–29 %) | I 1 tilstand |
| SPG7SPG7 matrix AAA peptidase subunit, paraplegin | Sjældent (1–4%) | I 1 tilstand |
| TGFB2transforming growth factor beta 2 | 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.
Snævrere træk
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 2026.10.17-8666dff2.
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Gratis forsendelse · Resultater på 6–8 uger
