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Træk
Rib fusion
Complete or partial merging of adjacent ribs.
Resumé
- Også kaldet
- Fused ribs
- Kropssystem
- Abnormality of the musculoskeletal system
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Denne 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/rib-fusion.json"
page <- fromJSON(url)
page$trait$nameRib fusionHP:0000902
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Læs de gener, der er knyttet til Rib fusion, og resten af dit genom, med én test.
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Bestil min Genome Test26 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.
- Nevoid Basal Cell Carcinoma (Gorlin) SyndromeReads 2 of these genesPTCH1SUFUAbout this report →
- CHRNG-Related Multiple Pterygium SyndromeReads 1 of these genesCHRNGAbout this report →
- Dyssegmental Dysplasia, Silverman-Handmaker TypeReads 1 of these genesHSPG2About this report →
- Greig Cephalopolysyndactyly SyndromeReads 1 of these genesGLI3About this report →
Show 22 more reports
- Radio-Tartaglia SyndromeReads 1 of these genesSPENAbout this report →
- Schwartz-Jampel Syndrome Type 1Reads 1 of these genesHSPG2About this report →
- ZTTK SyndromeReads 1 of these genesSONAbout this report →
- Müllerian Aplasia (MRKH Syndrome)Reads 1 of these genesTBX6About this report →
- Congenital Disorders of GlycosylationReads 7 of these genesCOG1DLL3MESP2HES7LFNGRIPPLY2About this report →
- MedulloblastomaReads 1 of these genesSUFUAbout this report →
- Rothmund-Thomson SyndromeReads 1 of these genesRECQL4About this report →
- Complex Neurodevelopmental Disorder (TRRAP, MYH10, RERE, SOX11)Reads 1 of these genesREREAbout this report →
- Syndromic CraniosynostosisReads 2 of these genesSKIRECQL4About this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 2 of these genesGLI3PTCH1About this report →
- Marfan Like SyndromesReads 1 of these genesSKIAbout this report →
- GPI Anchor Biosynthesis DefectsReads 1 of these genesPIGGAbout this report →
- Autoimmune DiseaseReads 1 of these genesCHRNGAbout this report →
- Lissencephaly Spectrum DisordersReads 1 of these genesACTBAbout this report →
- Intellectual DisabilityReads 3 of these genesNSD2PIGGANKRD11About this report →
- Microphthalmia, Anophthalmia & ColobomaReads 1 of these genesSOX2About this report →
- Inherited ThrombocytopeniasReads 1 of these genesACTBAbout this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesACTBAbout this report →
- Joubert Syndrome And Related DisordersReads 1 of these genesSUFUAbout this report →
- Dilated CardiomyopathyReads 1 of these genesPRDM16About this report →
- Epilepsy (Full Panel)Reads 1 of these genesCPLX1About this report →
- Inherited Neurodegenerative DisordersReads 1 of these genesLETM1About this report →
Læs de gener, der er knyttet til Rib fusion, og resten af dit genom, med én test.
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Bestil min Genome Test48 gener knyttet til Rib fusion
Ændringer i disse gener forårsager sjældne tilstande, hvor Rib fusion 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 |
|---|---|---|
| COG1component of oligomeric golgi complex 1 | Altid | I 2 tilstande |
| DLL3delta like canonical Notch ligand 3 | Altid | I 2 tilstande |
| DMRT2doublesex and mab-3 related transcription factor 2 | Altid | I 1 tilstand |
| MESP2mesoderm posterior bHLH transcription factor 2 | Altid | I 3 tilstande |
| HES7hes family bHLH transcription factor 7 | Meget ofte (80–99 %) | I 2 tilstande |
| LFNGLFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase | Meget ofte (80–99 %) | I 2 tilstande |
| RIPPLY2ripply transcriptional repressor 2 | Meget ofte (80–99 %) | I 1 tilstand |
| ROR2ROR family WNT receptor 2 | Meget ofte (80–99 %) | I 2 tilstande |
| TBX6T-box transcription factor 6 | Meget ofte (80–99 %) | I 1 tilstand |
| TMCO1transmembrane and coiled-coil domains 1 | Meget ofte (80–99 %) | I 2 tilstande |
| CPLX1complexin 1 | Ofte (30–79 %) | I 2 tilstande |
| CTBP1C-terminal binding protein 1 | Ofte (30–79 %) | I 2 tilstande |
| FAAP100FA core complex associated protein 100 | Ofte (30–79 %) | I 1 tilstand |
| FGFRL1fibroblast growth factor receptor like 1 | Ofte (30–79 %) | I 1 tilstand |
| GLI3GLI family zinc finger 3 | Ofte (30–79 %) | I 2 tilstande |
| LETM1leucine zipper and EF-hand containing transmembrane protein 1 | Ofte (30–79 %) | I 2 tilstande |
| NELFAnegative elongation factor complex member A | Ofte (30–79 %) | I 1 tilstand |
| NSD2nuclear receptor binding SET domain protein 2 | Ofte (30–79 %) | I 2 tilstande |
| NXNnucleoredoxin | Ofte (30–79 %) | I 1 tilstand |
| PIGGphosphatidylinositol glycan anchor biosynthesis class G (EMM blood group) | Ofte (30–79 %) | I 1 tilstand |
| PTCH1patched 1 | Ofte (30–79 %) | I 1 tilstand |
| PTCH2patched 2 | Ofte (30–79 %) | I 1 tilstand |
| SUFUSUFU negative regulator of hedgehog signaling | Ofte (30–79 %) | I 1 tilstand |
| WDR83OSWD repeat domain 83 opposite strand | Ofte (30–79 %) | I 1 tilstand |
| ACTBactin beta | Nogle gange (5–29 %) | I 1 tilstand |
| CASZ1castor zinc finger 1 | Nogle gange (5–29 %) | I 1 tilstand |
| CHRNGcholinergic receptor nicotinic gamma subunit | Nogle gange (5–29 %) | I 2 tilstande |
| GABRDgamma-aminobutyric acid type A receptor subunit delta | Nogle gange (5–29 %) | I 1 tilstand |
| HSPG2heparan sulfate proteoglycan 2 | Nogle gange (5–29 %) | I 1 tilstand |
| KCNAB2potassium voltage-gated channel subfamily A regulatory beta subunit 2 | Nogle gange (5–29 %) | I 1 tilstand |
| LUZP1leucine zipper protein 1 | Nogle gange (5–29 %) | I 1 tilstand |
| MMP23Bmatrix metallopeptidase 23B | Nogle gange (5–29 %) | I 1 tilstand |
| MYH3myosin heavy chain 3 | Nogle gange (5–29 %) | I 1 tilstand |
| ODC1ornithine decarboxylase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| PDPNpodoplanin | Nogle gange (5–29 %) | I 1 tilstand |
| PRDM16PR/SET domain 16 | Nogle gange (5–29 %) | I 1 tilstand |
| PRKCZprotein kinase C zeta | Nogle gange (5–29 %) | I 1 tilstand |
| REREarginine-glutamic acid dipeptide repeats | Nogle gange (5–29 %) | I 1 tilstand |
| SKISKI proto-oncogene | Nogle gange (5–29 %) | I 1 tilstand |
| SONSON DNA and RNA binding protein | Nogle gange (5–29 %) | I 2 tilstande |
Vis 8 gener mere
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| SPENspen family transcriptional repressor | Nogle gange (5–29 %) | I 1 tilstand |
| UBE4Bubiquitination factor E4B | Nogle gange (5–29 %) | I 1 tilstand |
| SH2B1SH2B adaptor protein 1 | Sjældent (1–4%) | I 1 tilstand |
| ANKRD11ankyrin repeat domain 11 | Ikke registreret | I 1 tilstand |
| MAP3K7mitogen-activated protein kinase kinase kinase 7 | Ikke registreret | I 1 tilstand |
| RECQL4RecQ like helicase 4 | Ikke registreret | I 1 tilstand |
| SIX6SIX homeobox 6 | Ikke registreret | I 1 tilstand |
| SOX2SRY-box transcription factor 2 | 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.
Snævrere træk
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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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.
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