Træk
Knee pain
An unpleasant sensation characterized by physical discomfort (such as pricking, throbbing, or aching) localized to the knee.
Resumé
- Også kaldet
- Pain under knee cap
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/knee-pain.json"
page <- fromJSON(url)
page$trait$nameLæs de gener, der er knyttet til Knee 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.
- Epiphyseal and Spondyloepiphyseal DysplasiasReads 6 of these genesCOL9A1COL9A2COL9A3COMPMATN3COL2A1About this report →
- Ghosal Haematodiaphyseal DysplasiaReads 1 of these genesTBXAS1About this report →
- Nail-Patella SyndromeReads 1 of these genesLMX1BAbout this report →
- VitreoretinopathyReads 5 of these genesCOL11A1COL9A1COL9A2COL9A3COL2A1About this report →
Show 17 more reports
- Otospondylomegaepiphyseal Dysplasia (OSMED)Reads 1 of these genesCOL2A1About this report →
- Achondrogenesis panelReads 1 of these genesCOL2A1About this report →
- Hypodontia and AnodontiaReads 1 of these genesLRP6About this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 2 of these genesGJB2GJB6About this report →
- Hearing Loss and DeafnessReads 3 of these genesCOL11A1GJB2GJB6About this report →
- Hereditary AmyloidosisReads 1 of these genesB2MAbout this report →
- LipodystrophyReads 1 of these genesBSCL2About this report →
- Ectodermal DysplasiasReads 1 of these genesGJB6About this report →
- Neonatal Diabetes MellitusReads 1 of these genesBSCL2About this report →
- Spinal Muscular AtrophyReads 1 of these genesBSCL2About this report →
- Diabetes MellitusReads 1 of these genesBSCL2About this report →
- Lysosomal Storage DiseaseReads 1 of these genesHYAL1About this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesBSCL2About this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesBSCL2About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesB2MAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 1 of these genesBSCL2About this report →
- Inherited Neurodegenerative DisordersReads 1 of these genesBSCL2About this report →
Læs de gener, der er knyttet til Knee pain, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test20 gener knyttet til Knee pain
Ændringer i disse gener forårsager sjældne tilstande, hvor Knee 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 |
|---|---|---|
| COL11A1collagen type XI alpha 1 chain | Altid | I 1 tilstand |
| COL9A1collagen type IX alpha 1 chain | Altid | I 2 tilstande |
| HYAL1hyaluronidase 1 | Altid | I 1 tilstand |
| LRP6LDL receptor related protein 6 | Altid | I 1 tilstand |
| PLD4phospholipase D family member 4 | Altid | I 1 tilstand |
| SLCO2A1solute carrier organic anion transporter family member 2A1 | Altid | I 2 tilstande |
| TBXAS1thromboxane A synthase 1 | Altid | I 1 tilstand |
| COL9A2collagen type IX alpha 2 chain | Ofte (30–79 %) | I 2 tilstande |
| COL9A3collagen type IX alpha 3 chain | Ofte (30–79 %) | I 2 tilstande |
| COMPcartilage oligomeric matrix protein | Ofte (30–79 %) | I 1 tilstand |
| MATN3matrilin 3 | Ofte (30–79 %) | I 1 tilstand |
| MMP13matrix metallopeptidase 13 | Ofte (30–79 %) | I 1 tilstand |
| TRAPPC2trafficking protein particle complex subunit 2 | Ofte (30–79 %) | I 1 tilstand |
| B2Mbeta-2-microglobulin | Nogle gange (5–29 %) | I 1 tilstand |
| BSCL2BSCL2 lipid droplet biogenesis associated, seipin | Nogle gange (5–29 %) | I 1 tilstand |
| COL2A1collagen type II alpha 1 chain | Nogle gange (5–29 %) | I 1 tilstand |
| LMX1BLIM homeobox transcription factor 1 beta | Nogle gange (5–29 %) | I 1 tilstand |
| TONSLtonsoku like, DNA repair protein | Nogle gange (5–29 %) | I 1 tilstand |
| GJB2gap junction protein beta 2 | Sjældent (1–4%) | I 1 tilstand |
| GJB6gap junction protein beta 6 | Sjældent (1–4%) | 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 2026.10.18-e609d43e.
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Gratis forsendelse · Resultater på 6–8 uger
