AtlasTræk
Broad ribs
Increased width of ribs
Resumé
- Også kaldet
- Wide ribs
- Kropssystem
- Abnormality of the musculoskeletal system
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/broad-ribs.json"
page <- fromJSON(url)
page$trait$nameLæs de gener, der er knyttet til Broad ribs, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test23 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.
- Mucopolysaccharidosis Type VI (Maroteaux-Lamy Syndrome)Reads 1 of these genesARSBAbout this report →
- Primary Failure of Tooth EruptionReads 1 of these genesPTH1RAbout this report →
- Juvenile Polyposis SyndromeReads 1 of these genesSMAD4About this report →
- Disorder of Copper MetabolismReads 1 of these genesATP7AAbout this report →
Show 19 more reports
- Mucolipidoses (ML II, ML III and ML IV)Reads 1 of these genesGNPTABAbout this report →
- Hereditary Hemorrhagic TelangiectasiaReads 1 of these genesSMAD4About this report →
- Sclerosing Bone Dysplasias (High Bone Mass)Reads 1 of these genesSOSTAbout this report →
- Lysosomal Storage DiseaseReads 3 of these genesARSKARSBGNPTABAbout this report →
- Epiphyseal and Spondyloepiphyseal DysplasiasReads 1 of these genesXYLT1About this report →
- Marfan Like SyndromesReads 1 of these genesFBN1About this report →
- Polycystic Kidney DiseaseReads 1 of these genesIFT140About this report →
- Aortic AneurysmReads 1 of these genesFBN1About this report →
- OsteopetrosisReads 1 of these genesAMER1About this report →
- Cutis LaxaReads 1 of these genesATP7AAbout this report →
- Hearing Loss and DeafnessReads 2 of these genesCOL11A1COL11A2About this report →
- Intellectual DisabilityReads 3 of these genesSETBP1SMAD4TFE3About this report →
- VitreoretinopathyReads 1 of these genesCOL11A1About this report →
- Spinal Muscular AtrophyReads 1 of these genesATP7AAbout this report →
- Osteogenesis ImperfectaReads 1 of these genesSERPINH1About this report →
- Rare Monogenic Autoinflammatory DiseasesReads 1 of these genesIL1RNAbout this report →
- Dilated CardiomyopathyReads 1 of these genesABCC9About this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesATP7AAbout this report →
- Retinitis PigmentosaReads 1 of these genesIFT140About this report →
Læs de gener, der er knyttet til Broad ribs, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test25 gener knyttet til Broad ribs
Ændringer i disse gener forårsager sjældne tilstande, hvor Broad ribs 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 |
|---|---|---|
| ARSKarylsulfatase family member K | Altid | I 1 tilstand |
| IFT140intraflagellar transport 140 | Altid | I 1 tilstand |
| IL1RNinterleukin 1 receptor antagonist | Altid | I 1 tilstand |
| PTDSS1phosphatidylserine synthase 1 | Altid | I 1 tilstand |
| PTH1Rparathyroid hormone 1 receptor | Altid | I 1 tilstand |
| SERPINH1serpin family H member 1 | Altid | I 1 tilstand |
| TMEM53transmembrane protein 53 | Altid | I 1 tilstand |
| COL11A1collagen type XI alpha 1 chain | Meget ofte (80–99 %) | I 1 tilstand |
| COL11A2collagen type XI alpha 2 chain | Meget ofte (80–99 %) | I 1 tilstand |
| ABCC9ATP binding cassette subfamily C member 9 | Ofte (30–79 %) | I 1 tilstand |
| DYMdymeclin | Ofte (30–79 %) | I 1 tilstand |
| KCNJ8potassium inwardly rectifying channel subfamily J member 8 | Ofte (30–79 %) | I 1 tilstand |
| NEK9NIMA related kinase 9 | Ofte (30–79 %) | I 1 tilstand |
| SETBP1SET binding protein 1 | Ofte (30–79 %) | I 2 tilstande |
| SMAD4SMAD family member 4 | Ofte (30–79 %) | I 1 tilstand |
| TFE3transcription factor binding to IGHM enhancer 3 | Ofte (30–79 %) | I 1 tilstand |
| WNT7AWnt family member 7A | Ofte (30–79 %) | I 1 tilstand |
| XYLT1xylosyltransferase 1 | Ofte (30–79 %) | I 1 tilstand |
| ADAMTS10ADAM metallopeptidase with thrombospondin type 1 motif 10 | Ikke registreret | I 1 tilstand |
| AMER1APC membrane recruitment protein 1 | Ikke registreret | I 1 tilstand |
| ARSBarylsulfatase B | Ikke registreret | I 1 tilstand |
| ATP7AATPase copper transporting alpha | Ikke registreret | I 1 tilstand |
| FBN1fibrillin 1 | Ikke registreret | I 1 tilstand |
| GNPTABN-acetylglucosamine-1-phosphate transferase subunits alpha and beta | Ikke registreret | I 1 tilstand |
| SOSTsclerostin | 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 2026.10.17-8666dff2.
AtlasFrom traits to your genome
Read the genes behind these traits in your own DNA.
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Gratis forsendelse · Resultater på 6–8 uger
