Tunnus
Hip pain
An unpleasant sensation characterized by physical discomfort (such as pricking, throbbing, or aching) localized to the hip.
Kokkuvõte
- Kehasüsteem
- Constitutional symptom
Selle lehe andmed
Lehe aadressile saab lisada .json või päringusse application/json, et lugeda seda JSON-vormingus.
library(jsonlite)
url <- "https://dantelabs.com/traits/hip-pain.json"
page <- fromJSON(url)
page$trait$nameLugege välja geenid, mis on seotud Hip pain-ga, ja kogu ülejäänud genoom ühe testiga.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test22 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.
- Restrictive Dermopathy (ZMPSTE24)Reads 1 of these genesZMPSTE24About this report →
- TRPV4-Related Skeletal DysplasiasReads 1 of these genesTRPV4About this report →
- LipodystrophyReads 3 of these genesBSCL2LMNAZMPSTE24About this report →
- Frontotemporal DementiaReads 3 of these genesHNRNPA1HNRNPA2B1VCPAbout this report →
Show 18 more reports
- Fibrodysplasia Ossificans ProgressivaReads 1 of these genesACVR1About this report →
- Otospondylomegaepiphyseal Dysplasia (OSMED)Reads 1 of these genesCOL2A1About this report →
- Distal MyopathiesReads 3 of these genesHNRNPA1HNRNPA2B1VCPAbout this report →
- Epiphyseal and Spondyloepiphyseal DysplasiasReads 2 of these genesCOL2A1MATN3About this report →
- Achondrogenesis panelReads 1 of these genesCOL2A1About this report →
- Charcot-Marie-Tooth DiseaseReads 4 of these genesTRPV4VCPBSCL2LMNAAbout this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 2 of these genesHNRNPA1VCPAbout this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesLMNAAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 4 of these genesTRPV4VCPBSCL2LMNAAbout this report →
- Neonatal Diabetes MellitusReads 1 of these genesBSCL2About this report →
- Inherited Neurodegenerative DisordersReads 4 of these genesHNRNPA1HNRNPA2B1VCPBSCL2About this report →
- VitreoretinopathyReads 1 of these genesCOL2A1About this report →
- Spinal Muscular AtrophyReads 1 of these genesBSCL2About this report →
- Diabetes MellitusReads 1 of these genesBSCL2About this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesLMNAAbout this report →
- Dilated CardiomyopathyReads 1 of these genesLMNAAbout this report →
- Lysosomal Storage DiseaseReads 1 of these genesHYAL1About this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesBSCL2About this report →
Lugege välja geenid, mis on seotud Hip pain-ga, ja kogu ülejäänud genoom ühe testiga.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test13 geeni on seotud tunnusega Hip pain
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Hip pain. Enamikul selle tunnusega inimestest ei ole ühtegi neist haigustest. Selles loendis olev geen ei ütle midagi kellegi enda genoomi kohta.
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| COL2A1collagen type II alpha 1 chain | Alati | Esineb 3 haiguses |
| MATN3matrilin 3 | Alati | Esineb 1 haiguses |
| SLC13A1solute carrier family 13 member 1 | Alati | Esineb 1 haiguses |
| ACVR1activin A receptor type 1 | Sageli (30–79%) | Esineb 1 haiguses |
| HNRNPA1heterogeneous nuclear ribonucleoprotein A1 | Sageli (30–79%) | Esineb 1 haiguses |
| HNRNPA2B1heterogeneous nuclear ribonucleoprotein A2/B1 | Sageli (30–79%) | Esineb 1 haiguses |
| HYAL1hyaluronidase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| TRPV4transient receptor potential cation channel subfamily V member 4 | Sageli (30–79%) | Esineb 1 haiguses |
| VCPvalosin containing protein | Sageli (30–79%) | Esineb 2 haiguses |
| BSCL2BSCL2 lipid droplet biogenesis associated, seipin | Mõnikord (5–29%) | Esineb 1 haiguses |
| LEMD3LEM domain containing 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| LMNAlamin A/C | Mõnikord (5–29%) | Esineb 1 haiguses |
| ZMPSTE24zinc metallopeptidase STE24 | Mõnikord (5–29%) | Esineb 1 haiguses |
Kui sageli see esineb geenist tulenevate seisunditega inimeste seas, kõige sagedamini nende kõigi seas, nagu on märgitud Inimese fenotüübi ontoloogias. Need lehed kirjeldavad tunnuseid ja nende taga olevaid uuringuid; need ei ole diagnoos ning sümptomite kohta tuleks küsida arstilt või geneetilt nõustajalt.
Laiemad tunnused
Allikas
- Inimese fenotüübi ontoloogia, versioon 2026-09-01: tunnus, selle nimetused, määratlus ja sellega seotud geenid. Lisateave leiab aadressilt hpo.jax.org.
- Andmeversioon 2026.10.19-9814e911.
From 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.
Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
