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Tunnus
Coxa valga
Coxa valga is a deformity of the hip in which the angle between the femoral shaft and the femoral neck is increased compared to age-adjusted values (about 150 degrees in newborns gradually reducing to 120-130 degrees in adults).
Kokkuvõte
- Teised nimetused
- Valgus hip
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Selle lehe andmed
Lehe aadressile saab lisada .json või päringusse application/json, et lugeda seda JSON-vormingus.
library(jsonlite)
url <- "https://dantelabs.com/traits/coxa-valga.json"
page <- fromJSON(url)
page$trait$nameCoxa valgaHP:0002673
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Lugege välja geenid, mis on seotud Coxa valga-ga, ja kogu ülejäänud genoom ühe testiga.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test69 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.
- Cantú SyndromeReads 2 of these genesABCC9KCNJ8About this report →
- Hereditary Multiple OsteochondromasReads 2 of these genesEXT1EXT2About this report →
- Achondrogenesis panelReads 2 of these genesCOL2A1TRIP11About this report →
- Overgrowth Syndromes (Sotos, Weaver, Tatton-Brown-Rahman, Malan)Reads 2 of these genesNFIXEZH2About this report →
Show 65 more reports
- Pseudohypoparathyroidism & GNAS-Inactivation DisordersReads 2 of these genesPDE4DPRKAR1AAbout this report →
- Au-Kline SyndromeReads 1 of these genesHNRNPKAbout this report →
- Desbuquois Dysplasia 1Reads 1 of these genesCANT1About this report →
- Dyssegmental Dysplasia, Silverman-Handmaker TypeReads 1 of these genesHSPG2About this report →
- GM1 Gangliosidosis and Morquio B SyndromeReads 1 of these genesGLB1About this report →
- Greig Cephalopolysyndactyly SyndromeReads 1 of these genesGLI3About this report →
- Marshall-Smith SyndromeReads 1 of these genesNFIXAbout this report →
- Mucopolysaccharidosis Type I (Hurler and Scheie Syndromes)Reads 1 of these genesIDUAAbout this report →
- Mucopolysaccharidosis Type IVA (Morquio A Syndrome)Reads 1 of these genesGALNSAbout this report →
- NGLY1 DeficiencyReads 1 of these genesNGLY1About this report →
- Restrictive Dermopathy (ZMPSTE24)Reads 1 of these genesZMPSTE24About this report →
- Saul-Wilson SyndromeReads 1 of these genesCOG4About this report →
- Schwartz-Jampel Syndrome Type 1Reads 1 of these genesHSPG2About this report →
- SHOX Deficiency (Leri-Weill and Langer Dysplasia)Reads 1 of these genesSHOXAbout this report →
- SLC10A7-Related Skeletal Dysplasia With Amelogenesis ImperfectaReads 1 of these genesSLC10A7About this report →
- Cleidocranial DysplasiaReads 1 of these genesCBFBAbout this report →
- Otospondylomegaepiphyseal Dysplasia (OSMED)Reads 1 of these genesCOL2A1About this report →
- TRIP11-Related Skeletal DysplasiaReads 1 of these genesTRIP11About this report →
- Congenital Disorders of GlycosylationReads 7 of these genesCOG4COG8COG1EXT2SLC35A2B3GALT6About this report →
- Epiphyseal and Spondyloepiphyseal DysplasiasReads 2 of these genesCOL2A1XYLT1About this report →
- Lysosomal Storage DiseaseReads 5 of these genesGNPTABFUCA1GALNSGLB1IDUAAbout this report →
- LipodystrophyReads 2 of these genesLMNAZMPSTE24About this report →
- Disorder of Copper MetabolismReads 1 of these genesATP7AAbout this report →
- Hereditary Arterial CalcificationReads 1 of these genesENPP1About this report →
- Monogenic Precocious PubertyReads 1 of these genesDLK1About this report →
- Mucolipidoses (ML II, ML III and ML IV)Reads 1 of these genesGNPTABAbout this report →
- Cutis LaxaReads 2 of these genesATP7ASLC2A10About this report →
- Carney Complex & Hereditary Adrenal Cushing SyndromeReads 1 of these genesPRKAR1AAbout this report →
- Periventricular Nodular HeterotopiaReads 1 of these genesFLNAAbout this report →
- Sclerosing Bone Dysplasias (High Bone Mass)Reads 1 of these genesTGFB1About this report →
- Ehlers-Danlos SyndromeReads 2 of these genesB3GALT6B4GALT7About this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 1 of these genesFLNAAbout this report →
- Inflammatory Bowel Diseases (IBD)Reads 1 of these genesTGFB1About this report →
- Hearing Loss and DeafnessReads 4 of these genesSLC12A2GJB2GJB6COL11A1About this report →
- Intellectual DisabilityReads 6 of these genesHNRNPH1HNRNPRARID1BATRXRPS6KA3WNK3About this report →
- VitreoretinopathyReads 2 of these genesCOL2A1COL11A1About this report →
- Alpha-Mannosidosis and Other GlycoproteinosesReads 1 of these genesFUCA1About this report →
- Aicardi-Goutieres SyndromeReads 1 of these genesIFIH1About this report →
- Hereditary Rickets (Hypophosphatemic and Vitamin D-Dependent)Reads 1 of these genesENPP1About this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesLMNAAbout this report →
- Osteogenesis ImperfectaReads 2 of these genesKDELR2IFIH1About this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 2 of these genesGJB2GJB6About this report →
- Marfan Like SyndromesReads 1 of these genesBGNAbout this report →
- Coffin-Siris SyndromeReads 1 of these genesARID1BAbout this report →
- Type I InterferonopathiesReads 1 of these genesIFIH1About this report →
- Dilated CardiomyopathyReads 2 of these genesLMNAABCC9About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesFLNAAbout this report →
- Ectodermal DysplasiasReads 1 of these genesGJB6About this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 1 of these genesATRXAbout this report →
- Charcot-Marie-Tooth DiseaseReads 2 of these genesLMNAATP7AAbout this report →
- Noonan SyndromeReads 1 of these genesMAPK1About this report →
- Syndromic CraniosynostosisReads 1 of these genesRAB23About this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 1 of these genesGLI3About this report →
- Spinal Muscular AtrophyReads 1 of these genesATP7AAbout this report →
- Inherited ThrombocytopeniasReads 1 of these genesRBM8AAbout this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesLMNAAbout this report →
- Rare Monogenic Autoinflammatory DiseasesReads 1 of these genesIFIH1About this report →
- Inherited Neurodegenerative DisordersReads 3 of these genesSIL1ATP7AIFIH1About this report →
- DNA Repair DiseaseReads 1 of these genesERCC6About this report →
- Epilepsy (Full Panel)Reads 2 of these genesFLNASLC35A2About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesSIL1About this report →
- Rare Hereditary Peripheral NeuropathiesReads 2 of these genesLMNAATP7AAbout this report →
- Hypertrophic CardiomyopathyReads 1 of these genesMAPK1About this report →
- Other Inherited LeukodystrophiesReads 1 of these genesIFIH1About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesIFIH1About this report →
Lugege välja geenid, mis on seotud Coxa valga-ga, ja kogu ülejäänud genoom ühe testiga.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test82 geeni on seotud tunnusega Coxa valga
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Coxa valga. Enamikul selle tunnusega inimestest ei ole ühtegi neist haigustest. Selles loendis olev geen ei ütle midagi kellegi enda genoomi kohta.
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| COG4component of oligomeric golgi complex 4 | Alati | Esineb 1 haiguses |
| EXTL3exostosin like glycosyltransferase 3 | Alati | Esineb 1 haiguses |
| FAM177A1family with sequence similarity 177 member A1 | Alati | Esineb 1 haiguses |
| FLNAfilamin A | Alati | Esineb 4 haiguses |
| HNRNPH1heterogeneous nuclear ribonucleoprotein H1 | Alati | Esineb 1 haiguses |
| LMNAlamin A/C | Alati | Esineb 2 haiguses |
| RBSNrabenosyn, RAB effector | Alati | Esineb 1 haiguses |
| SLC12A2solute carrier family 12 member 2 | Alati | Esineb 1 haiguses |
| TOMM7translocase of outer mitochondrial membrane 7 | Alati | Esineb 1 haiguses |
| ABCC9ATP binding cassette subfamily C member 9 | Väga sageli (80–99%) | Esineb 2 haiguses |
| KCNJ8potassium inwardly rectifying channel subfamily J member 8 | Väga sageli (80–99%) | Esineb 1 haiguses |
| AFF3ALF transcription elongation factor 3 | Sageli (30–79%) | Esineb 1 haiguses |
| CANT1calcium activated nucleotidase 1 | Sageli (30–79%) | Esineb 2 haiguses |
| COG8component of oligomeric golgi complex 8 | Sageli (30–79%) | Esineb 1 haiguses |
| COL2A1collagen type II alpha 1 chain | Sageli (30–79%) | Esineb 2 haiguses |
| CSGALNACT1chondroitin sulfate N-acetylgalactosaminyltransferase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| GNPTABN-acetylglucosamine-1-phosphate transferase subunits alpha and beta | Sageli (30–79%) | Esineb 1 haiguses |
| HNRNPKheterogeneous nuclear ribonucleoprotein K | Sageli (30–79%) | Esineb 1 haiguses |
| HSPG2heparan sulfate proteoglycan 2 | Sageli (30–79%) | Esineb 2 haiguses |
| NFIXnuclear factor I X | Sageli (30–79%) | Esineb 1 haiguses |
| PDE4Dphosphodiesterase 4D | Sageli (30–79%) | Esineb 1 haiguses |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Sageli (30–79%) | Esineb 1 haiguses |
| RBM8ARNA binding motif protein 8A | Sageli (30–79%) | Esineb 2 haiguses |
| SIL1SIL1 nucleotide exchange factor | Sageli (30–79%) | Esineb 2 haiguses |
| SLC10A7solute carrier family 10 member 7 | Sageli (30–79%) | Esineb 1 haiguses |
| SLC35B2solute carrier family 35 member B2 | Sageli (30–79%) | Esineb 1 haiguses |
| TRIP11thyroid hormone receptor interactor 11 | Sageli (30–79%) | Esineb 1 haiguses |
| XYLT1xylosyltransferase 1 | Sageli (30–79%) | Esineb 3 haiguses |
| ZMPSTE24zinc metallopeptidase STE24 | Sageli (30–79%) | Esineb 1 haiguses |
| ARCN1archain 1 coat protein complex I subunit delta | Mõnikord (5–29%) | Esineb 1 haiguses |
| ATP7AATPase copper transporting alpha | Mõnikord (5–29%) | Esineb 2 haiguses |
| BCRBCR activator of RhoGEF and GTPase | Mõnikord (5–29%) | Esineb 1 haiguses |
| CBFBcore-binding factor subunit beta | Mõnikord (5–29%) | Esineb 1 haiguses |
| COG1component of oligomeric golgi complex 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CRKLCRK like proto-oncogene, adaptor protein | Mõnikord (5–29%) | Esineb 1 haiguses |
| DLK1delta like non-canonical Notch ligand 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DVL1dishevelled segment polarity protein 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DVL3dishevelled segment polarity protein 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ENPP1ectonucleotide pyrophosphatase/phosphodiesterase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| EXT1exostosin glycosyltransferase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
Näita veel 42 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| EXT2exostosin glycosyltransferase 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| FBXO22F-box protein 22 | Mõnikord (5–29%) | Esineb 1 haiguses |
| FZD2frizzled class receptor 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GTF2E2general transcription factor IIE subunit 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HNRNPRheterogeneous nuclear ribonucleoprotein R | Mõnikord (5–29%) | Esineb 1 haiguses |
| KDELR2KDEL endoplasmic reticulum protein retention receptor 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MAPK1mitogen-activated protein kinase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MEG3maternally expressed 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NGLY1N-glycanase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NRCAMneuronal cell adhesion molecule | Mõnikord (5–29%) | Esineb 1 haiguses |
| OTUD5OTU deubiquitinase 5 | Mõnikord (5–29%) | Esineb 1 haiguses |
| POP1POP1 ribonuclease P/MRP subunit | Mõnikord (5–29%) | Esineb 1 haiguses |
| RTL1retrotransposon Gag like 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SLC2A10solute carrier family 2 member 10 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SLC35A2solute carrier family 35 member A2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TGFB1transforming growth factor beta 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| WNT5AWnt family member 5A | Mõnikord (5–29%) | Esineb 1 haiguses |
| GJB2gap junction protein beta 2 | Harva (1–4%) | Esineb 1 haiguses |
| GJB6gap junction protein beta 6 | Harva (1–4%) | Esineb 1 haiguses |
| GLI3GLI family zinc finger 3 | Harva (1–4%) | Esineb 1 haiguses |
| ADAMTSL2ADAMTS like 2 | Pole registreeritud | Esineb 1 haiguses |
| ARID1BAT-rich interaction domain 1B | Pole registreeritud | Esineb 1 haiguses |
| ATRXATRX chromatin remodeler | Pole registreeritud | Esineb 1 haiguses |
| B3GALT6beta-1,3-galactosyltransferase 6 | Pole registreeritud | Esineb 1 haiguses |
| B4GALT7beta-1,4-galactosyltransferase 7 | Pole registreeritud | Esineb 1 haiguses |
| BGNbiglycan | Pole registreeritud | Esineb 1 haiguses |
| COL11A1collagen type XI alpha 1 chain | Pole registreeritud | Esineb 1 haiguses |
| EEDembryonic ectoderm development | Pole registreeritud | Esineb 1 haiguses |
| EIF2AK3eukaryotic translation initiation factor 2 alpha kinase 3 | Pole registreeritud | Esineb 1 haiguses |
| ERCC6ERCC excision repair 6, chromatin remodeling factor | Pole registreeritud | Esineb 1 haiguses |
| EZH2enhancer of zeste 2 polycomb repressive complex 2 subunit | Pole registreeritud | Esineb 1 haiguses |
| FUCA1alpha-L-fucosidase 1 | Pole registreeritud | Esineb 1 haiguses |
| GALNSgalactosamine (N-acetyl)-6-sulfatase | Pole registreeritud | Esineb 1 haiguses |
| GLB1galactosidase beta 1 | Pole registreeritud | Esineb 2 haiguses |
| IDUAalpha-L-iduronidase | Pole registreeritud | Esineb 1 haiguses |
| IFIH1interferon induced with helicase C domain 1 | Pole registreeritud | Esineb 1 haiguses |
| MGAT2alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase | Pole registreeritud | Esineb 1 haiguses |
| ORC1origin recognition complex subunit 1 | Pole registreeritud | Esineb 1 haiguses |
| RAB23RAB23, member RAS oncogene family | Pole registreeritud | Esineb 1 haiguses |
| RPS6KA3ribosomal protein S6 kinase A3 | Pole registreeritud | Esineb 1 haiguses |
| SHOXSHOX homeobox | Pole registreeritud | Esineb 1 haiguses |
| WNK3WNK lysine deficient protein kinase 3 | Pole registreeritud | Esineb 1 haiguses |
Kui sageli see esineb geenist tulenevate seisunditega inimeste seas, kõige sagedamini nende kõigi seas, nagu on märgitud Inimese fenotüübi ontoloogias. Need lehed kirjeldavad tunnuseid ja nende taga olevaid uuringuid; need ei ole diagnoos ning sümptomite kohta tuleks küsida arstilt või geneetilt nõustajalt.
Kitsamad tunnused
Laiemad tunnused
Allikas
- Inimese fenotüübi ontoloogia, versioon 2026-09-01: tunnus, selle nimetused, määratlus ja sellega seotud geenid. Lisateave leiab aadressilt hpo.jax.org.
- Andmeversioon 2026.10.19-9814e911.
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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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Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
