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Egenskap
Coxa vara
Coxa vara includes all forms of decrease of the femoral neck shaft angle (the angle between the neck and the shaft of the femur) to less than 120 degrees.
Sammendrag
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Denne 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/coxa-vara.json"
page <- fromJSON(url)
page$trait$nameCoxa varaHP:0002812
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Logg innSpørSekvenser genomet ditt↗
Les genene knyttet til Coxa vara, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test46 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.
- Epiphyseal and Spondyloepiphyseal DysplasiasReads 9 of these genesCOL2A1FN1COL9A1SLC26A2XYLT1COL9A2About this report →
- Hereditary Multiple OsteochondromasReads 2 of these genesEXT1EXT2About this report →
- Immuno-Osseous DysplasiasReads 2 of these genesRMRPRNU4ATACAbout this report →
- Achondrogenesis panelReads 2 of these genesCOL2A1SLC26A2About this report →
Show 42 more reports
- Desbuquois Dysplasia 1Reads 1 of these genesCANT1About this report →
- Dyssegmental Dysplasia, Silverman-Handmaker TypeReads 1 of these genesHSPG2About this report →
- Marshall-Smith SyndromeReads 1 of these genesNFIXAbout this report →
- Meier-Gorlin Syndrome 3 (ORC6)Reads 1 of these genesORC6About this report →
- Microcephalic Osteodysplastic Primordial Dwarfism Type IIReads 1 of these genesPCNTAbout this report →
- Progressive Pseudorheumatoid DysplasiaReads 1 of these genesCCN6About this report →
- RNU4ATAC Spectrum DisorderReads 1 of these genesRNU4ATACAbout this report →
- Schmid Metaphyseal ChondrodysplasiaReads 1 of these genesCOL10A1About this report →
- Schwartz-Jampel Syndrome Type 1Reads 1 of these genesHSPG2About this report →
- Spondylometaphyseal Dysplasia With Cone-Rod DystrophyReads 1 of these genesPCYT1AAbout this report →
- TRPV4-Related Skeletal DysplasiasReads 1 of these genesTRPV4About this report →
- Osteogenesis ImperfectaReads 5 of these genesCRTAPATP6V0A2FKBP10KDELR2SERPINF1About this report →
- VitreoretinopathyReads 4 of these genesCOL2A1COL9A1COL9A2COL9A3About this report →
- Cutis LaxaReads 3 of these genesATP6V0A2ATP7ASLC2A10About this report →
- Hereditary Rickets (Hypophosphatemic and Vitamin D-Dependent)Reads 2 of these genesDMP1ENPP1About this report →
- Cleidocranial DysplasiaReads 1 of these genesRUNX2About this report →
- FLNB-Related Skeletal Dysplasia (Larsen Spectrum)Reads 1 of these genesFLNBAbout this report →
- Inherited ArthropathiesReads 1 of these genesPRG4About this report →
- Otospondylomegaepiphyseal Dysplasia (OSMED)Reads 1 of these genesCOL2A1About this report →
- Shwachman-Diamond SyndromeReads 1 of these genesSBDSAbout this report →
- Disorder of Copper MetabolismReads 1 of these genesATP7AAbout this report →
- Hereditary Arterial CalcificationReads 1 of these genesENPP1About this report →
- Overgrowth Syndromes (Sotos, Weaver, Tatton-Brown-Rahman, Malan)Reads 1 of these genesNFIXAbout this report →
- Cornelia de Lange SyndromeReads 1 of these genesRAD21About this report →
- Rare Inherited Bone Marrow Failure SyndromesReads 1 of these genesDNAJC21About this report →
- Familial Glucocorticoid DeficiencyReads 1 of these genesNDC1About this report →
- Charcot-Marie-Tooth DiseaseReads 3 of these genesTRPV4ATP7AAIFM1About this report →
- Severe Congenital NeutropeniaReads 1 of these genesSRP54About this report →
- OsteopetrosisReads 1 of these genesTCIRG1About this report →
- Zellweger Spectrum & Peroxisome Biogenesis DisordersReads 1 of these genesPEX5About this report →
- Rare Hereditary Peripheral NeuropathiesReads 4 of these genesPEX5TRPV4ATP7AAIFM1About this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 1 of these genesAIFM1About this report →
- Syndromic CraniosynostosisReads 1 of these genesMEGF8About this report →
- Congenital Disorders of GlycosylationReads 2 of these genesATP6V0A2EXT2About this report →
- Spinal Muscular AtrophyReads 1 of these genesATP7AAbout this report →
- Other Inborn Errors of ImmunityReads 2 of these genesRMRPSBDSAbout this report →
- Leigh SyndromeReads 1 of these genesAIFM1About this report →
- Other Inherited LeukodystrophiesReads 1 of these genesPEX5About this report →
- Inherited Neurodegenerative DisordersReads 2 of these genesPEX5ATP7AAbout this report →
- Hearing Loss and DeafnessReads 1 of these genesAIFM1About this report →
- Primary Mitochondrial DiseaseReads 1 of these genesAIFM1About this report →
- Epilepsy (Full Panel)Reads 1 of these genesUFSP2About this report →
Les genene knyttet til Coxa vara, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test65 gener knyttet til Coxa vara
Endringer i disse genene forårsaker sjeldne tilstander der Coxa vara 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 |
|---|---|---|
| COL10A1collagen type X alpha 1 chain | Alltid | I 2 tilstander |
| CRTAPcartilage associated protein | Alltid | I 1 tilstand |
| NDC1NDC1 transmembrane nucleoporin | Alltid | I 1 tilstand |
| NKX3-2NK3 homeobox 2 | Alltid | I 1 tilstand |
| RPL13ribosomal protein L13 | Alltid | I 1 tilstand |
| ATP6V0A2ATPase H+ transporting V0 subunit a2 | Svært ofte (80–99 %) | I 2 tilstander |
| COL2A1collagen type II alpha 1 chain | Svært ofte (80–99 %) | I 8 tilstander |
| DMP1dentin matrix acidic phosphoprotein 1 | Svært ofte (80–99 %) | I 1 tilstand |
| ENPP1ectonucleotide pyrophosphatase/phosphodiesterase 1 | Svært ofte (80–99 %) | I 1 tilstand |
| FN1fibronectin 1 | Svært ofte (80–99 %) | I 2 tilstander |
| IHHIndian hedgehog signaling molecule | Svært ofte (80–99 %) | I 2 tilstander |
| PCNTpericentrin | Svært ofte (80–99 %) | I 2 tilstander |
| PCYT1Aphosphate cytidylyltransferase 1A, choline | Svært ofte (80–99 %) | I 2 tilstander |
| PRG4proteoglycan 4 | Svært ofte (80–99 %) | I 2 tilstander |
| CANT1calcium activated nucleotidase 1 | Ofte (30–79 %) | I 2 tilstander |
| COL27A1collagen type XXVII alpha 1 chain | Ofte (30–79 %) | I 1 tilstand |
| COL9A1collagen type IX alpha 1 chain | Ofte (30–79 %) | I 2 tilstander |
| CSGALNACT1chondroitin sulfate N-acetylgalactosaminyltransferase 1 | Ofte (30–79 %) | I 1 tilstand |
| EXTL3exostosin like glycosyltransferase 3 | Ofte (30–79 %) | I 1 tilstand |
| HSPG2heparan sulfate proteoglycan 2 | Ofte (30–79 %) | I 2 tilstander |
| NFIXnuclear factor I X | Ofte (30–79 %) | I 1 tilstand |
| PEX5peroxisomal biogenesis factor 5 | Ofte (30–79 %) | I 1 tilstand |
| RAD21RAD21 cohesin complex component | Ofte (30–79 %) | I 1 tilstand |
| RMRPRNA component of mitochondrial RNA processing endoribonuclease | Ofte (30–79 %) | I 1 tilstand |
| RNU4ATACRNA, U4atac small nuclear | Ofte (30–79 %) | I 1 tilstand |
| RSPRY1ring finger and SPRY domain containing 1 | Ofte (30–79 %) | I 1 tilstand |
| RUNX2RUNX family transcription factor 2 | Ofte (30–79 %) | I 2 tilstander |
| SLC26A2solute carrier family 26 member 2 | Ofte (30–79 %) | I 1 tilstand |
| TRPV4transient receptor potential cation channel subfamily V member 4 | Ofte (30–79 %) | I 2 tilstander |
| XYLT1xylosyltransferase 1 | Ofte (30–79 %) | I 1 tilstand |
| ATP7AATPase copper transporting alpha | Noen ganger (5–29 %) | I 1 tilstand |
| CCN6cellular communication network factor 6 | Noen ganger (5–29 %) | I 2 tilstander |
| COL9A2collagen type IX alpha 2 chain | Noen ganger (5–29 %) | I 1 tilstand |
| COL9A3collagen type IX alpha 3 chain | Noen ganger (5–29 %) | I 1 tilstand |
| DVL1dishevelled segment polarity protein 1 | Noen ganger (5–29 %) | I 1 tilstand |
| DVL3dishevelled segment polarity protein 3 | Noen ganger (5–29 %) | I 1 tilstand |
| DYMdymeclin | Noen ganger (5–29 %) | I 1 tilstand |
| FKBP10FKBP prolyl isomerase 10 | Noen ganger (5–29 %) | I 2 tilstander |
| FZD2frizzled class receptor 2 | Noen ganger (5–29 %) | I 1 tilstand |
| KDELR2KDEL endoplasmic reticulum protein retention receptor 2 | Noen ganger (5–29 %) | I 1 tilstand |
Vis 25 gener til
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| MATN3matrilin 3 | Noen ganger (5–29 %) | I 1 tilstand |
| MEGF8multiple EGF like domains 8 | Noen ganger (5–29 %) | I 1 tilstand |
| SLC2A10solute carrier family 2 member 10 | Noen ganger (5–29 %) | I 1 tilstand |
| SLC4A10solute carrier family 4 member 10 | Noen ganger (5–29 %) | I 1 tilstand |
| TONSLtonsoku like, DNA repair protein | Noen ganger (5–29 %) | I 2 tilstander |
| TRAPPC2trafficking protein particle complex subunit 2 | Noen ganger (5–29 %) | I 2 tilstander |
| TTI1TELO2 interacting protein 1 | Noen ganger (5–29 %) | I 1 tilstand |
| UFSP2UFM1 specific peptidase 2 | Noen ganger (5–29 %) | I 1 tilstand |
| WNT5AWnt family member 5A | Noen ganger (5–29 %) | I 1 tilstand |
| COMPcartilage oligomeric matrix protein | Sjelden (1–4%) | I 1 tilstand |
| AIFM1apoptosis inducing factor mitochondria associated 1 | Ikke registrert | I 1 tilstand |
| CFAP410cilia and flagella associated protein 410 | Ikke registrert | I 1 tilstand |
| DDRGK1DDRGK domain containing 1 | Ikke registrert | I 1 tilstand |
| DNAJC21DnaJ heat shock protein family (Hsp40) member C21 | Ikke registrert | I 1 tilstand |
| EXT1exostosin glycosyltransferase 1 | Ikke registrert | I 1 tilstand |
| EXT2exostosin glycosyltransferase 2 | Ikke registrert | I 1 tilstand |
| FLNBfilamin B | Ikke registrert | I 1 tilstand |
| MMP13matrix metallopeptidase 13 | Ikke registrert | I 1 tilstand |
| ORC6origin recognition complex subunit 6 | Ikke registrert | I 1 tilstand |
| POP1POP1 ribonuclease P/MRP subunit | Ikke registrert | I 1 tilstand |
| SBDSSBDS ribosome maturation factor | Ikke registrert | I 1 tilstand |
| SERPINF1serpin family F member 1 | Ikke registrert | I 1 tilstand |
| SRP54signal recognition particle 54 | Ikke registrert | I 1 tilstand |
| TBX4T-box transcription factor 4 | Ikke registrert | I 1 tilstand |
| TCIRG1T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 | 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.
AtlasHvem vi hjelperVår vitenskapProdukterResultater
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From 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.
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