Tunnus
Partial hip dislocation
Kliiniline nimetus: Hip subluxation
A partial dislocation of the hip joint, whereby the head of the femur is partially displaced from the socket.
Kokkuvõte
- Teised nimetused
- Subluxation involving the hip joint
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-subluxation.json"
page <- fromJSON(url)
page$trait$nameLugege välja geenid, mis on seotud Partial hip dislocation-ga, ja kogu ülejäänud genoom ühe testiga.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test16 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.
- Smith-Lemli-Opitz SyndromeReads 1 of these genesDHCR7About this report →
- Mucolipidoses (ML II, ML III and ML IV)Reads 1 of these genesGNPTABAbout this report →
- Overgrowth Syndromes (Sotos, Weaver, Tatton-Brown-Rahman, Malan)Reads 1 of these genesNFIXAbout this report →
- Ehlers-Danlos SyndromeReads 2 of these genesPLOD1B3GALT6About this report →
Show 12 more reports
- Aicardi-Goutieres SyndromeReads 1 of these genesIFIH1About this report →
- Type I InterferonopathiesReads 1 of these genesIFIH1About this report →
- OsteopetrosisReads 1 of these genesOSTM1About this report →
- Primary Lymphoedema & Lymphatic MalformationsReads 1 of these genesFAT4About this report →
- Epilepsy (Full Panel)Reads 3 of these genesLMNB2THOC2SLC35A2About this report →
- Congenital Disorders of GlycosylationReads 2 of these genesSLC35A2B3GALT6About this report →
- Osteogenesis ImperfectaReads 1 of these genesIFIH1About this report →
- Rare Monogenic Autoinflammatory DiseasesReads 1 of these genesIFIH1About this report →
- Intellectual DisabilityReads 2 of these genesTHOC2CTCFAbout this report →
- Lysosomal Storage DiseaseReads 1 of these genesGNPTABAbout this report →
- Other Inherited LeukodystrophiesReads 1 of these genesIFIH1About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesIFIH1About this report →
Lugege välja geenid, mis on seotud Partial hip dislocation-ga, ja kogu ülejäänud genoom ühe testiga.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test26 geeni on seotud tunnusega Partial hip dislocation
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Partial hip dislocation. 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 |
|---|---|---|
| FAT4FAT atypical cadherin 4 | Alati | Esineb 1 haiguses |
| GET4guided entry of tail-anchored proteins factor 4 | Alati | Esineb 1 haiguses |
| UNC13Aunc-13 homolog A | Alati | Esineb 1 haiguses |
| OSTM1osteoclastogenesis associated transmembrane protein 1 | Sageli (30–79%) | Esineb 1 haiguses |
| ZNF407zinc finger protein 407 | Sageli (30–79%) | Esineb 1 haiguses |
| AFF4ALF transcription elongation factor 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| BICRABRD4 interacting chromatin remodeling complex associated protein | Mõnikord (5–29%) | Esineb 1 haiguses |
| DOT1LDOT1 like histone lysine methyltransferase | Mõnikord (5–29%) | Esineb 1 haiguses |
| EIF4A3eukaryotic translation initiation factor 4A3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GNB2G protein subunit beta 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GNPTABN-acetylglucosamine-1-phosphate transferase subunits alpha and beta | Mõnikord (5–29%) | Esineb 1 haiguses |
| KIF22kinesin family member 22 | Mõnikord (5–29%) | Esineb 1 haiguses |
| LMNB2lamin B2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NFIXnuclear factor I X | Mõnikord (5–29%) | Esineb 1 haiguses |
| PLOD1procollagen-lysine,2-oxoglutarate 5-dioxygenase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RMP64ribonuclease MRP subunit p64 | Mõnikord (5–29%) | Esineb 1 haiguses |
| THOC2THO complex subunit 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TONSLtonsoku like, DNA repair protein | Mõnikord (5–29%) | Esineb 1 haiguses |
| TRAPPC12trafficking protein particle complex subunit 12 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CTCFCCCTC-binding factor | Harva (1–4%) | Esineb 1 haiguses |
| SLC35A2solute carrier family 35 member A2 | Harva (1–4%) | Esineb 1 haiguses |
| B3GALT6beta-1,3-galactosyltransferase 6 | Pole registreeritud | Esineb 1 haiguses |
| DDR2discoidin domain receptor tyrosine kinase 2 | Pole registreeritud | Esineb 1 haiguses |
| DHCR77-dehydrocholesterol reductase | Pole registreeritud | Esineb 1 haiguses |
| EIF2AK3eukaryotic translation initiation factor 2 alpha kinase 3 | Pole registreeritud | Esineb 1 haiguses |
| IFIH1interferon induced with helicase C domain 1 | Pole registreeritud | 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 2026.10.17-8666dff2.
From traits to your genome
Read the genes behind these traits in your own DNA.
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Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
