AtlasTræk
Partial hip dislocation
Klinisk navn: Hip subluxation
A partial dislocation of the hip joint, whereby the head of the femur is partially displaced from the socket.
Resumé
- Også kaldet
- Subluxation involving the hip joint
AtlasDenne 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/hip-subluxation.json"
page <- fromJSON(url)
page$trait$nameLæs de gener, der er knyttet til Partial hip dislocation, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min 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 →
Læs de gener, der er knyttet til Partial hip dislocation, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test26 gener knyttet til Partial hip dislocation
Ændringer i disse gener forårsager sjældne tilstande, hvor Partial hip dislocation 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 |
|---|---|---|
| FAT4FAT atypical cadherin 4 | Altid | I 1 tilstand |
| GET4guided entry of tail-anchored proteins factor 4 | Altid | I 1 tilstand |
| UNC13Aunc-13 homolog A | Altid | I 1 tilstand |
| OSTM1osteoclastogenesis associated transmembrane protein 1 | Ofte (30–79 %) | I 1 tilstand |
| ZNF407zinc finger protein 407 | Ofte (30–79 %) | I 1 tilstand |
| AFF4ALF transcription elongation factor 4 | Nogle gange (5–29 %) | I 1 tilstand |
| BICRABRD4 interacting chromatin remodeling complex associated protein | Nogle gange (5–29 %) | I 1 tilstand |
| DOT1LDOT1 like histone lysine methyltransferase | Nogle gange (5–29 %) | I 1 tilstand |
| EIF4A3eukaryotic translation initiation factor 4A3 | Nogle gange (5–29 %) | I 1 tilstand |
| GNB2G protein subunit beta 2 | Nogle gange (5–29 %) | I 1 tilstand |
| GNPTABN-acetylglucosamine-1-phosphate transferase subunits alpha and beta | Nogle gange (5–29 %) | I 1 tilstand |
| KIF22kinesin family member 22 | Nogle gange (5–29 %) | I 1 tilstand |
| LMNB2lamin B2 | Nogle gange (5–29 %) | I 1 tilstand |
| NFIXnuclear factor I X | Nogle gange (5–29 %) | I 1 tilstand |
| PLOD1procollagen-lysine,2-oxoglutarate 5-dioxygenase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| RMP64ribonuclease MRP subunit p64 | Nogle gange (5–29 %) | I 1 tilstand |
| THOC2THO complex subunit 2 | Nogle gange (5–29 %) | I 1 tilstand |
| TONSLtonsoku like, DNA repair protein | Nogle gange (5–29 %) | I 1 tilstand |
| TRAPPC12trafficking protein particle complex subunit 12 | Nogle gange (5–29 %) | I 1 tilstand |
| CTCFCCCTC-binding factor | Sjældent (1–4%) | I 1 tilstand |
| SLC35A2solute carrier family 35 member A2 | Sjældent (1–4%) | I 1 tilstand |
| B3GALT6beta-1,3-galactosyltransferase 6 | Ikke registreret | I 1 tilstand |
| DDR2discoidin domain receptor tyrosine kinase 2 | Ikke registreret | I 1 tilstand |
| DHCR77-dehydrocholesterol reductase | Ikke registreret | I 1 tilstand |
| EIF2AK3eukaryotic translation initiation factor 2 alpha kinase 3 | Ikke registreret | I 1 tilstand |
| IFIH1interferon induced with helicase C domain 1 | Ikke registreret | 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 2026.10.19-9814e911.
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Gratis forsendelse · Resultater på 6–8 uger
