Kenmerk
Dislocated radial head
A dislocation of the head of the radius from its socket in the elbow joint.
Samenvatting
- Ook bekend als
- Congenital radial head dislocation, Dislocated radius, Dislocation of radial head, Dislocation of the radial head, Radial dislocation, Radial head dislocation, Radial head dislocation/subluxation
Deze pagina als gegevens
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page$trait$nameLees de genen die aan Dislocated radial head gekoppeld zijn, en de rest van uw genoom, met één test.
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Mijn Genome Test bestellen35 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.
- Ehlers-Danlos SyndromeReads 6 of these genesB4GALT7SLC39A13COL1A1COL5A1COL5A2B3GALT6About this report →
- Caffey DiseaseReads 1 of these genesCOL1A1About this report →
- Campomelic DysplasiaReads 1 of these genesSOX9About this report →
- CHRNG-Related Multiple Pterygium SyndromeReads 1 of these genesCHRNGAbout this report →
Show 31 more reports
- Floating-Harbor SyndromeReads 1 of these genesSRCAPAbout this report →
- Hajdu-Cheney SyndromeReads 1 of these genesNOTCH2About this report →
- L1 SyndromeReads 1 of these genesL1CAMAbout this report →
- Meier-Gorlin Syndrome 7 (CDC45)Reads 1 of these genesCDC45About this report →
- Nail-Patella SyndromeReads 1 of these genesLMX1BAbout this report →
- NOG-Related Symphalangism Spectrum DisorderReads 1 of these genesNOGAbout this report →
- RNU4ATAC Spectrum DisorderReads 1 of these genesRNU4ATACAbout this report →
- Spondyloepimetaphyseal Dysplasia with Joint Laxity Type 3Reads 1 of these genesEXOC6BAbout this report →
- Spondyloepiphyseal Dysplasia With Congenital Joint DislocationsReads 1 of these genesCHST3About this report →
- Alagille SyndromeReads 1 of these genesNOTCH2About this report →
- Immuno-Osseous DysplasiasReads 1 of these genesRNU4ATACAbout this report →
- Carney Complex & Hereditary Adrenal Cushing SyndromeReads 1 of these genesPRKAR1AAbout this report →
- Multiple Synostoses Syndrome (FGF9)Reads 1 of these genesNOGAbout this report →
- Pseudohypoparathyroidism & GNAS-Inactivation DisordersReads 1 of these genesPRKAR1AAbout this report →
- Periventricular Nodular HeterotopiaReads 1 of these genesFLNAAbout this report →
- Cornelia de Lange SyndromeReads 1 of these genesNIPBLAbout this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 1 of these genesFLNAAbout this report →
- Osteogenesis ImperfectaReads 2 of these genesBMP1COL1A1About this report →
- Marfan Like SyndromesReads 1 of these genesSKIAbout this report →
- Coffin-Siris SyndromeReads 1 of these genesARID1BAbout this report →
- Inherited Congenital Heart DefectsReads 1 of these genesFLNAAbout this report →
- Intellectual DisabilityReads 4 of these genesARID1BASXL1CREBBPEP300About this report →
- Autoimmune DiseaseReads 1 of these genesCHRNGAbout this report →
- Syndromic CraniosynostosisReads 1 of these genesSKIAbout this report →
- Congenital Disorders of GlycosylationReads 2 of these genesB3GAT3B3GALT6About this report →
- Microphthalmia, Anophthalmia & ColobomaReads 1 of these genesERCC1About this report →
- DNA Repair DiseaseReads 1 of these genesERCC1About this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesL1CAMAbout this report →
- Other Inherited LeukodystrophiesReads 1 of these genesALDH3A2About this report →
- Inherited Neurodegenerative DisordersReads 2 of these genesL1CAMALDH3A2About this report →
- Epilepsy (Full Panel)Reads 1 of these genesFLNAAbout this report →
Lees de genen die aan Dislocated radial head gekoppeld zijn, en de rest van uw genoom, met één test.
Vanaf $ 449Gratis verzending · Resultaten binnen 6–8 weken
Mijn Genome Test bestellen47 genen gekoppeld aan Dislocated radial head
Veranderingen in deze genen veroorzaken zeldzame aandoeningen waarbij Dislocated radial head voorkomt. De meeste mensen met dit kenmerk hebben geen van die aandoeningen, en een gen op deze lijst zegt niets over het eigen genoom van iemand.
| Gen | Hoe vaak het voorkomt | Aandoeningen |
|---|---|---|
| CHST3carbohydrate sulfotransferase 3 | Altijd | In 2 aandoeningen |
| DONSONDNA replication fork stabilization factor DONSON | Altijd | In 2 aandoeningen |
| ERCC1ERCC excision repair 1, endonuclease non-catalytic subunit | Altijd | In 1 aandoening |
| ERI1exoribonuclease 1 | Altijd | In 1 aandoening |
| EXOC6Bexocyst complex component 6B | Altijd | In 1 aandoening |
| MAP3K7mitogen-activated protein kinase kinase kinase 7 | Altijd | In 2 aandoeningen |
| PPFIA3PPFI scaffold protein A3 | Altijd | In 1 aandoening |
| B3GAT3beta-1,3-glucuronyltransferase 3 | Vaak (30–79%) | In 1 aandoening |
| B4GALT7beta-1,4-galactosyltransferase 7 | Vaak (30–79%) | In 1 aandoening |
| CD96CD96 molecule | Vaak (30–79%) | In 2 aandoeningen |
| COL27A1collagen type XXVII alpha 1 chain | Vaak (30–79%) | In 1 aandoening |
| DVL1dishevelled segment polarity protein 1 | Vaak (30–79%) | In 1 aandoening |
| EXTL3exostosin like glycosyltransferase 3 | Vaak (30–79%) | In 1 aandoening |
| FLNAfilamin A | Vaak (30–79%) | In 3 aandoeningen |
| FZD2frizzled class receptor 2 | Vaak (30–79%) | In 1 aandoening |
| GSCgoosecoid homeobox | Vaak (30–79%) | In 1 aandoening |
| L1CAML1 cell adhesion molecule | Vaak (30–79%) | In 1 aandoening |
| ROR2ROR family WNT receptor 2 | Vaak (30–79%) | In 1 aandoening |
| SCARF2scavenger receptor class F member 2 | Vaak (30–79%) | In 2 aandoeningen |
| SLC39A13solute carrier family 39 member 13 | Vaak (30–79%) | In 1 aandoening |
| SOX9SRY-box transcription factor 9 | Vaak (30–79%) | In 1 aandoening |
| WNT5AWnt family member 5A | Vaak (30–79%) | In 1 aandoening |
| AFF3ALF transcription elongation factor 3 | Soms (5–29%) | In 1 aandoening |
| BMP1bone morphogenetic protein 1 | Soms (5–29%) | In 1 aandoening |
| CDC45cell division cycle 45 | Soms (5–29%) | In 1 aandoening |
| CLCN3Cl-/H+ antiporter 3 | Soms (5–29%) | In 1 aandoening |
| COL1A1collagen type I alpha 1 chain | Soms (5–29%) | In 1 aandoening |
| COL5A1collagen type V alpha 1 chain | Soms (5–29%) | In 1 aandoening |
| COL5A2collagen type V alpha 2 chain | Soms (5–29%) | In 1 aandoening |
| LMX1BLIM homeobox transcription factor 1 beta | Soms (5–29%) | In 1 aandoening |
| RNU4ATACRNA, U4atac small nuclear | Soms (5–29%) | In 1 aandoening |
| SKISKI proto-oncogene | Soms (5–29%) | In 1 aandoening |
| SRCAPSnf2 related CREBBP activator protein | Soms (5–29%) | In 2 aandoeningen |
| ALDH3A2aldehyde dehydrogenase 3 family member A2 | Zelden (1–4%) | In 1 aandoening |
| ARID1BAT-rich interaction domain 1B | Niet vastgelegd | In 1 aandoening |
| ASXL1ASXL transcriptional regulator 1 | Niet vastgelegd | In 1 aandoening |
| ATRATR checkpoint kinase | Niet vastgelegd | In 1 aandoening |
| B3GALT6beta-1,3-galactosyltransferase 6 | Niet vastgelegd | In 1 aandoening |
| CHRNGcholinergic receptor nicotinic gamma subunit | Niet vastgelegd | In 1 aandoening |
| CREBBPCREB binding lysine acetyltransferase | Niet vastgelegd | In 1 aandoening |
Toon nog 7 genen
| Gen | Hoe vaak het voorkomt | Aandoeningen |
|---|---|---|
| EP300EP300 lysine acetyltransferase | Niet vastgelegd | In 1 aandoening |
| KIF22kinesin family member 22 | Niet vastgelegd | In 1 aandoening |
| NIPBLNIPBL cohesin loading factor | Niet vastgelegd | In 1 aandoening |
| NOGnoggin | Niet vastgelegd | In 1 aandoening |
| NOTCH2notch receptor 2 | Niet vastgelegd | In 1 aandoening |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Niet vastgelegd | In 1 aandoening |
| TBX15T-box transcription factor 15 | Niet vastgelegd | In 1 aandoening |
Hoe vaak dit voorkomt bij mensen met een van de aandoeningen van het gen, de hoogste frequentie binnen die aandoeningen, zoals de Human Phenotype Ontology dit vastlegt. Deze pagina's beschrijven kenmerken en het onderzoek erachter; het zijn geen diagnose, en over symptomen kunt u het best een arts of genetisch adviseur raadplegen.
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Waar dit vandaan komt
- De Human Phenotype Ontology, release 2026-09-01: het kenmerk, de namen, de definitie en de genen die ermee verbonden zijn. Meer informatie vindt u op hpo.jax.org.
- Gegevensrelease 2026.10.19-9814e911.
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