AtlasEgenskap
Limb pain
Chronic pain in the limbs with no clear focal etiology.
Sammendrag
- Også kalt
- Pain in extremities
AtlasDenne siden som data
Legg til .json etter adressen til siden, eller be om application/json, for å lese den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/limb-pain.json"
page <- fromJSON(url)
page$trait$nameLes genene knyttet til Limb pain, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test30 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.
- Caffey DiseaseReads 1 of these genesCOL1A1About this report →
- Von Hippel-Lindau DiseaseReads 1 of these genesVHLAbout this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 4 of these genesATL1ATL3SPTLC1SPTLC2About this report →
- Hepatic Porphyria DisordersReads 2 of these genesCPOXHMBSAbout this report →
Show 26 more reports
- Otospondylomegaepiphyseal Dysplasia (OSMED)Reads 1 of these genesCOL2A1About this report →
- Epiphyseal and Spondyloepiphyseal DysplasiasReads 2 of these genesCOL2A1FN1About this report →
- PorphyriaReads 2 of these genesCPOXHMBSAbout this report →
- Ehlers-Danlos SyndromeReads 3 of these genesCOL1A1COL5A1COL5A2About this report →
- Achondrogenesis panelReads 1 of these genesCOL2A1About this report →
- Sclerosing Bone Dysplasias (High Bone Mass)Reads 1 of these genesTGFB1About this report →
- Inflammatory Bowel Diseases (IBD)Reads 1 of these genesTGFB1About this report →
- Systemic Lupus ErythematosusReads 1 of these genesTREX1About this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 2 of these genesSPTLC1SPTLC2About this report →
- Aicardi-Goutieres SyndromeReads 1 of these genesTREX1About this report →
- PolycythemiaReads 1 of these genesVHLAbout this report →
- Kidney CancerReads 1 of these genesVHLAbout this report →
- Hereditary Pheochromocytoma and ParagangliomaReads 1 of these genesVHLAbout this report →
- Type I InterferonopathiesReads 1 of these genesTREX1About this report →
- Urinary and Renal System TumourReads 1 of these genesVHLAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 4 of these genesATL1ATL3SPTLC1SPTLC2About this report →
- Glycogen Storage DiseaseReads 1 of these genesGYS1About this report →
- Autoimmune DiseaseReads 1 of these genesTREX1About this report →
- VitreoretinopathyReads 1 of these genesCOL2A1About this report →
- Osteogenesis ImperfectaReads 1 of these genesCOL1A1About this report →
- Rare Monogenic Autoinflammatory DiseasesReads 1 of these genesTREX1About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesPRKRAAbout this report →
- Inherited Neurodegenerative DisordersReads 3 of these genesATL1SPTLC1TREX1About this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesATL1About this report →
- Other Inherited LeukodystrophiesReads 1 of these genesTREX1About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesTREX1About this report →
Les genene knyttet til Limb pain, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test18 gener knyttet til Limb pain
Endringer i disse genene forårsaker sjeldne tilstander der Limb pain forekommer. De fleste med denne egenskapen har ingen av disse tilstandene, og et gen på denne listen sier ingenting om noens eget genom.
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| GYS1glycogen synthase 1 | Alltid | I 1 tilstand |
| ATL1atlastin GTPase 1 | Ofte (30–79 %) | I 1 tilstand |
| ATL3atlastin GTPase 3 | Ofte (30–79 %) | I 1 tilstand |
| COL2A1collagen type II alpha 1 chain | Ofte (30–79 %) | I 1 tilstand |
| CPOXcoproporphyrinogen oxidase | Ofte (30–79 %) | I 1 tilstand |
| FN1fibronectin 1 | Ofte (30–79 %) | I 1 tilstand |
| HMBShydroxymethylbilane synthase | Ofte (30–79 %) | I 1 tilstand |
| SPTLC1serine palmitoyltransferase long chain base subunit 1 | Ofte (30–79 %) | I 1 tilstand |
| SPTLC2serine palmitoyltransferase long chain base subunit 2 | Ofte (30–79 %) | I 1 tilstand |
| TGFB1transforming growth factor beta 1 | Ofte (30–79 %) | I 1 tilstand |
| CCND1cyclin D1 | Noen ganger (5–29 %) | I 1 tilstand |
| COL1A1collagen type I alpha 1 chain | Noen ganger (5–29 %) | I 1 tilstand |
| COL5A1collagen type V alpha 1 chain | Noen ganger (5–29 %) | I 1 tilstand |
| COL5A2collagen type V alpha 2 chain | Noen ganger (5–29 %) | I 1 tilstand |
| TRAPPC2trafficking protein particle complex subunit 2 | Noen ganger (5–29 %) | I 1 tilstand |
| VHLvon Hippel-Lindau tumor suppressor | Noen ganger (5–29 %) | I 1 tilstand |
| PRKRAprotein activator of interferon induced protein kinase EIF2AK2 | Ikke registrert | I 1 tilstand |
| TREX1three prime repair exonuclease 1 | Ikke registrert | I 1 tilstand |
Hvor ofte dette forekommer hos personer med en av genets tilstander, oppgitt som den hyppigste forekomsten blant dem, slik Human Phenotype Ontology registrerer den. Disse sidene beskriver egenskaper og forskningen bak dem. De er ikke en diagnose, og om symptomer bør du spørre lege eller genetisk rådgiver.
Smalere egenskaper
Bredere egenskaper
Slik er informasjonen samlet
- Human Phenotype Ontology, versjon 2026-09-01: egenskapen, navnene på den, definisjonen og genene som er knyttet til den. Les mer på hpo.jax.org.
- Datautgave 2026.10.19-9814e911.
AtlasFrom traits to your genome
Read the genes behind these traits in your own DNA.
The Genome Test sequences nearly all of your DNA, not a preset panel, so every gene on these pages is in your data. Premium adds 810+ physician-ready reports.
Gratis frakt · Resultater på 6–8 uker
