Požymis
Partial hip dislocation
Klinikinis pavadinimas: Hip subluxation
A partial dislocation of the hip joint, whereby the head of the femur is partially displaced from the socket.
Santrauka
- Taip pat vadinama
- Subluxation involving the hip joint
Ši puslapis kaip duomenys
Norėdami perskaityti jį kaip JSON, pridėkite .json prie puslapio adreso arba nurodykite application/json.
library(jsonlite)
url <- "https://dantelabs.com/traits/hip-subluxation.json"
page <- fromJSON(url)
page$trait$nameVienu tyrimu sužinokite genus, susijusius su Partial hip dislocation, ir kitą jūsų genomo dalį.
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Įsigyti savo 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.
- FAT4-Related Neurodevelopmental DisorderReads 1 of these genesFAT4About this report →
- Marshall-Smith SyndromeReads 1 of these genesNFIXAbout this report →
- Smith-Lemli-Opitz SyndromeReads 1 of these genesDHCR7About this report →
- Spondylo-Meta-Epiphyseal Dysplasia, Short Limb-Abnormal Calcification TypeReads 1 of these genesDDR2About this report →
Show 18 more reports
- UNC13A-Related Neurodevelopmental DisordersReads 1 of these genesUNC13AAbout 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 →
- Aicardi-Goutieres SyndromeReads 1 of these genesIFIH1About this report →
- Coffin-Siris SyndromeReads 1 of these genesBICRAAbout 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 →
- Inherited Neurodegenerative DisordersReads 1 of these genesIFIH1About this report →
Vienu tyrimu sužinokite genus, susijusius su Partial hip dislocation, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test26 genų susiję su Partial hip dislocation
Šių genų pakitimai sukelia retas ligas, kuriose pasireiškia Partial hip dislocation. Dauguma žmonių, turinčių šį požymį, neturi nė vienos iš tų ligų, o šiame sąraše esantis genas nieko nesako apie kieno nors paties genomą.
| Genas | Kaip dažnai pasireiškia | Ligos |
|---|---|---|
| FAT4FAT atypical cadherin 4 | Visada | 1 ligoje |
| GET4guided entry of tail-anchored proteins factor 4 | Visada | 1 ligoje |
| UNC13Aunc-13 homolog A | Visada | 1 ligoje |
| OSTM1osteoclastogenesis associated transmembrane protein 1 | Dažnai (30–79%) | 1 ligoje |
| ZNF407zinc finger protein 407 | Dažnai (30–79%) | 1 ligoje |
| AFF4ALF transcription elongation factor 4 | Kartais (5–29%) | 1 ligoje |
| BICRABRD4 interacting chromatin remodeling complex associated protein | Kartais (5–29%) | 1 ligoje |
| DOT1LDOT1 like histone lysine methyltransferase | Kartais (5–29%) | 1 ligoje |
| EIF4A3eukaryotic translation initiation factor 4A3 | Kartais (5–29%) | 1 ligoje |
| GNB2G protein subunit beta 2 | Kartais (5–29%) | 1 ligoje |
| GNPTABN-acetylglucosamine-1-phosphate transferase subunits alpha and beta | Kartais (5–29%) | 1 ligoje |
| KIF22kinesin family member 22 | Kartais (5–29%) | 1 ligoje |
| LMNB2lamin B2 | Kartais (5–29%) | 1 ligoje |
| NFIXnuclear factor I X | Kartais (5–29%) | 1 ligoje |
| PLOD1procollagen-lysine,2-oxoglutarate 5-dioxygenase 1 | Kartais (5–29%) | 1 ligoje |
| RMP64ribonuclease MRP subunit p64 | Kartais (5–29%) | 1 ligoje |
| THOC2THO complex subunit 2 | Kartais (5–29%) | 1 ligoje |
| TONSLtonsoku like, DNA repair protein | Kartais (5–29%) | 1 ligoje |
| TRAPPC12trafficking protein particle complex subunit 12 | Kartais (5–29%) | 1 ligoje |
| CTCFCCCTC-binding factor | Retai (1–4 %) | 1 ligoje |
| SLC35A2solute carrier family 35 member A2 | Retai (1–4 %) | 1 ligoje |
| B3GALT6beta-1,3-galactosyltransferase 6 | Neužfiksuota | 1 ligoje |
| DDR2discoidin domain receptor tyrosine kinase 2 | Neužfiksuota | 1 ligoje |
| DHCR77-dehydrocholesterol reductase | Neužfiksuota | 1 ligoje |
| EIF2AK3eukaryotic translation initiation factor 2 alpha kinase 3 | Neužfiksuota | 1 ligoje |
| IFIH1interferon induced with helicase C domain 1 | Neužfiksuota | 1 ligoje |
Kaip dažnai šis požymis pasitaiko žmonėms, turintiems vieną iš geno sukeliamų ligų, ir kuris dažnis tarp jų didžiausias, pagal Žmogaus fenotipo ontologijos duomenis. Šiuose puslapiuose aprašomi požymiai ir juos grindžiantys tyrimai; tai nėra diagnozė, o su simptomais kreipkitės į gydytoją ar genetikos konsultantą.
Platesni požymiai
Iš kur tai žinoma
- Žmogaus fenotipo ontologija, 2026-09-01 leidimas: požymis, jo pavadinimai, apibrėžimas ir su juo susiję genai. Daugiau sužinokite svetainėje hpo.jax.org.
- Duomenų leidimas 2026.10.19-9814e911.
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Read the genes behind these traits in your own DNA.
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