AtlasEgenskap
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.
Sammendrag
- Også kalt
- Subluxation involving the hip joint
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/hip-subluxation.json"
page <- fromJSON(url)
page$trait$nameLes genene knyttet til Partial hip dislocation, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt 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 →
Les genene knyttet til Partial hip dislocation, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test26 gener knyttet til Partial hip dislocation
Endringer i disse genene forårsaker sjeldne tilstander der Partial hip dislocation 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 |
|---|---|---|
| FAT4FAT atypical cadherin 4 | Alltid | I 1 tilstand |
| GET4guided entry of tail-anchored proteins factor 4 | Alltid | I 1 tilstand |
| UNC13Aunc-13 homolog A | Alltid | 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 | Noen ganger (5–29 %) | I 1 tilstand |
| BICRABRD4 interacting chromatin remodeling complex associated protein | Noen ganger (5–29 %) | I 1 tilstand |
| DOT1LDOT1 like histone lysine methyltransferase | Noen ganger (5–29 %) | I 1 tilstand |
| EIF4A3eukaryotic translation initiation factor 4A3 | Noen ganger (5–29 %) | I 1 tilstand |
| GNB2G protein subunit beta 2 | Noen ganger (5–29 %) | I 1 tilstand |
| GNPTABN-acetylglucosamine-1-phosphate transferase subunits alpha and beta | Noen ganger (5–29 %) | I 1 tilstand |
| KIF22kinesin family member 22 | Noen ganger (5–29 %) | I 1 tilstand |
| LMNB2lamin B2 | Noen ganger (5–29 %) | I 1 tilstand |
| NFIXnuclear factor I X | Noen ganger (5–29 %) | I 1 tilstand |
| PLOD1procollagen-lysine,2-oxoglutarate 5-dioxygenase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| RMP64ribonuclease MRP subunit p64 | Noen ganger (5–29 %) | I 1 tilstand |
| THOC2THO complex subunit 2 | Noen ganger (5–29 %) | I 1 tilstand |
| TONSLtonsoku like, DNA repair protein | Noen ganger (5–29 %) | I 1 tilstand |
| TRAPPC12trafficking protein particle complex subunit 12 | Noen ganger (5–29 %) | I 1 tilstand |
| CTCFCCCTC-binding factor | Sjelden (1–4%) | I 1 tilstand |
| SLC35A2solute carrier family 35 member A2 | Sjelden (1–4%) | I 1 tilstand |
| B3GALT6beta-1,3-galactosyltransferase 6 | Ikke registrert | I 1 tilstand |
| DDR2discoidin domain receptor tyrosine kinase 2 | Ikke registrert | I 1 tilstand |
| DHCR77-dehydrocholesterol reductase | Ikke registrert | I 1 tilstand |
| EIF2AK3eukaryotic translation initiation factor 2 alpha kinase 3 | Ikke registrert | I 1 tilstand |
| IFIH1interferon induced with helicase C domain 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.
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
