AtlasEgenskap
Bowing of outer large bone of the forearm
Klinisk navn: Radial bowing
A bending or abnormal curvature of the radius.
Sammendrag
- Også kalt
- Bowed radii, Bowed radius, Bowing of radius bone of the forearm
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/radial-bowing.json"
page <- fromJSON(url)
page$trait$nameLes genene knyttet til Bowing of outer large bone of the forearm, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test34 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.
- Achondrogenesis panelReads 3 of these genesCOL2A1SLC26A2GDF5About this report →
- FGFR3-Related Chondrodysplasias (Achondroplasia and Related Conditions)Reads 1 of these genesFGFR3About this report →
- Greig Cephalopolysyndactyly SyndromeReads 1 of these genesGLI3About this report →
- Microcephalic Osteodysplastic Primordial Dwarfism Type IIReads 1 of these genesPCNTAbout this report →
Show 30 more reports
- SHOX Deficiency (Leri-Weill and Langer Dysplasia)Reads 1 of these genesSHOXAbout this report →
- TRPV4-Related Skeletal DysplasiasReads 1 of these genesTRPV4About this report →
- FLNB-Related Skeletal Dysplasia (Larsen Spectrum)Reads 1 of these genesFLNBAbout this report →
- Otospondylomegaepiphyseal Dysplasia (OSMED)Reads 1 of these genesCOL2A1About this report →
- Epiphyseal and Spondyloepiphyseal DysplasiasReads 2 of these genesCOL2A1SLC26A2About this report →
- Inherited Congenital Heart DefectsReads 2 of these genesTBX5FLNAAbout this report →
- Multiple Synostoses Syndrome (FGF9)Reads 1 of these genesGDF5About this report →
- Periventricular Nodular HeterotopiaReads 1 of these genesFLNAAbout this report →
- Syndromic CraniosynostosisReads 2 of these genesFGFR3IFT43About this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 1 of these genesFLNAAbout this report →
- VitreoretinopathyReads 2 of these genesCOL2A1COL11A1About this report →
- Ellis-van Creveld Syndrome and Cranioectodermal DysplasiaReads 1 of these genesIFT43About this report →
- Hereditary Rickets (Hypophosphatemic and Vitamin D-Dependent)Reads 1 of these genesFGF23About this report →
- Meckel SyndromeReads 1 of these genesTMEM67About this report →
- Hereditary AmyloidosisReads 1 of these genesB2MAbout this report →
- Nephronophthisis and Senior-Løken SyndromeReads 1 of these genesTMEM67About this report →
- Ehlers-Danlos SyndromeReads 1 of these genesB3GALT6About this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 1 of these genesGLI3About this report →
- Inherited ThrombocytopeniasReads 1 of these genesHOXA11About this report →
- Osteogenesis ImperfectaReads 1 of these genesP3H1About this report →
- Joubert Syndrome And Related DisordersReads 1 of these genesTMEM67About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesTMEM67About this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesTRPV4About this report →
- Retinitis PigmentosaReads 1 of these genesIFT43About this report →
- Hearing Loss and DeafnessReads 1 of these genesCOL11A1About this report →
- Congenital Disorders of GlycosylationReads 1 of these genesB3GALT6About this report →
- Epilepsy (Full Panel)Reads 1 of these genesFLNAAbout this report →
- Other Inborn Errors of ImmunityReads 1 of these genesB2MAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 1 of these genesTRPV4About this report →
- Inherited Neurodegenerative DisordersReads 1 of these genesTMEM67About this report →
Les genene knyttet til Bowing of outer large bone of the forearm, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test27 gener knyttet til Bowing of outer large bone of the forearm
Endringer i disse genene forårsaker sjeldne tilstander der Bowing of outer large bone of the forearm 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 |
|---|---|---|
| FGF23fibroblast growth factor 23 | Alltid | I 1 tilstand |
| FGFR3fibroblast growth factor receptor 3 | Alltid | I 1 tilstand |
| IFT43intraflagellar transport 43 | Alltid | I 1 tilstand |
| LBRlamin B receptor | Alltid | I 1 tilstand |
| TBX5T-box transcription factor 5 | Alltid | I 1 tilstand |
| TMEM67transmembrane protein 67 | Alltid | I 1 tilstand |
| SHOXSHOX homeobox | Svært ofte (80–99 %) | I 3 tilstander |
| WNT7AWnt family member 7A | Svært ofte (80–99 %) | I 3 tilstander |
| COL2A1collagen type II alpha 1 chain | Ofte (30–79 %) | I 1 tilstand |
| GLI3GLI family zinc finger 3 | Ofte (30–79 %) | I 1 tilstand |
| IHHIndian hedgehog signaling molecule | Ofte (30–79 %) | I 1 tilstand |
| PRKG2protein kinase cGMP-dependent 2 | Ofte (30–79 %) | I 1 tilstand |
| ROR2ROR family WNT receptor 2 | Ofte (30–79 %) | I 1 tilstand |
| SLC26A2solute carrier family 26 member 2 | Noen ganger (5–29 %) | I 1 tilstand |
| TRPV4transient receptor potential cation channel subfamily V member 4 | Noen ganger (5–29 %) | I 1 tilstand |
| B2Mbeta-2-microglobulin | Ikke registrert | I 1 tilstand |
| B3GALT6beta-1,3-galactosyltransferase 6 | Ikke registrert | I 1 tilstand |
| CCN2cellular communication network factor 2 | Ikke registrert | I 1 tilstand |
| COL11A1collagen type XI alpha 1 chain | Ikke registrert | I 1 tilstand |
| FLNAfilamin A | Ikke registrert | I 1 tilstand |
| FLNBfilamin B | Ikke registrert | I 2 tilstander |
| GDF5growth differentiation factor 5 | Ikke registrert | I 1 tilstand |
| HOXA11homeobox A11 | Ikke registrert | I 1 tilstand |
| MMP13matrix metallopeptidase 13 | Ikke registrert | I 1 tilstand |
| NPR2natriuretic peptide receptor 2 | Ikke registrert | I 1 tilstand |
| P3H1prolyl 3-hydroxylase 1 | Ikke registrert | I 1 tilstand |
| PCNTpericentrin | 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.
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Gratis frakt · Resultater på 6–8 uker
