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Özellik
Pes valgus
An outward (valgus) deviation of the calcaneus relative to the longitudinal axis of the lower leg at the talocalcaneal (subtalar) joint, such that the heel is everted.
Özet
- Diğer adları
- Valgus foot deformity
- Vücut sistemi
- Abnormality of limbs
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Veriyi JSON olarak okumak için sayfa adresinin sonuna .json ekleyin veya application/json isteyin.
library(jsonlite)
url <- "https://dantelabs.com/traits/pes-valgus.json"
page <- fromJSON(url)
page$trait$namePes valgusHP:0008081
AtlasKimlere Yardımcı OluyoruzBilimimizÜrünlerSonuçlar
Giriş YapSorGenomunuzu dizileyin↗
Pes valgus ile bağlantılı genleri ve genomunuzun geri kalanını tek bir testle okuyun.
$449'den başlayanÜcretsiz kargo · Sonuçlar 6–8 hafta içinde
Genome Test'imi al54 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.
- Congenital Muscular DystrophiesReads 6 of these genesCOL12A1COL6A1COL6A2COL6A3LARGE1TRIP4About this report →
- DeSanto-Shinawi SyndromeReads 1 of these genesWACAbout this report →
- Dravet SyndromeReads 1 of these genesSCN1AAbout this report →
- EBF3-Related Neurodevelopmental Disorder (HADDS)Reads 1 of these genesEBF3About this report →
Show 50 more reports
- FDXR-Related Mitochondrial DisorderReads 1 of these genesFDXRAbout this report →
- SCN4A-Related Congenital MyopathyReads 1 of these genesSCN4AAbout this report →
- Carey-Fineman-Ziter SyndromeReads 1 of these genesMYMXAbout this report →
- Congenital MyopathiesReads 3 of these genesMYPNTPM2TPM3About this report →
- Epilepsy (Full Panel)Reads 9 of these genesFLNAGABRA1GABRG2PCDH19RNU2-2SCN1AAbout this report →
- Intellectual DisabilityReads 9 of these genesTCF4HNRNPRMBD5PUF60SLC16A2PCDH19About this report →
- Familial Hemiplegic MigraineReads 1 of these genesSCN1AAbout this report →
- Familial Periodic ParalysisReads 1 of these genesSCN4AAbout this report →
- Thyroid Hormone Resistance, Transport & Metabolism DefectsReads 1 of these genesSLC16A2About this report →
- Spinal Muscular AtrophyReads 3 of these genesBSCL2GARS1REEP1About this report →
- Charcot-Marie-Tooth DiseaseReads 5 of these genesBSCL2GARS1HK1REEP1SH3TC2About this report →
- Limb-Girdle Muscular DystrophyReads 3 of these genesCOL6A1COL6A2COL6A3About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 3 of these genesTOR1ACOL6A3SCN4AAbout this report →
- Achondrogenesis panelReads 1 of these genesGDF5About this report →
- Hereditary Episodic AtaxiasReads 1 of these genesSCN2AAbout this report →
- Multiple Synostoses Syndrome (FGF9)Reads 1 of these genesGDF5About this report →
- Overgrowth Syndromes (Sotos, Weaver, Tatton-Brown-Rahman, Malan)Reads 1 of these genesNSD1About this report →
- Rare Hereditary Peripheral NeuropathiesReads 7 of these genesFDXRBSCL2GARS1HK1REEP1SCN9AAbout this report →
- Periventricular Nodular HeterotopiaReads 1 of these genesFLNAAbout this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 1 of these genesFLNAAbout this report →
- Hypertrophic CardiomyopathyReads 3 of these genesNSD1MYPNSPRED2About this report →
- Ellis-van Creveld Syndrome and Cranioectodermal DysplasiaReads 1 of these genesWDR19About this report →
- Hereditary Spastic ParaplegiaReads 3 of these genesBSCL2CAPN1REEP1About this report →
- Familial Glucocorticoid DeficiencyReads 1 of these genesNDC1About this report →
- Pyruvate Kinase Deficiency and Other Red Cell Enzyme DisordersReads 1 of these genesHK1About this report →
- Epiphyseal and Spondyloepiphyseal DysplasiasReads 1 of these genesCOL9A3About this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 1 of these genesNSD1About this report →
- Long QT SyndromeReads 1 of these genesCACNA1CAbout this report →
- Marfan Like SyndromesReads 1 of these genesFBN1About this report →
- HyperinsulinismReads 1 of these genesHK1About this report →
- LipodystrophyReads 1 of these genesBSCL2About this report →
- Dilated CardiomyopathyReads 2 of these genesBAG3MYPNAbout this report →
- Aortic AneurysmReads 1 of these genesFBN1About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesFLNAAbout this report →
- Myofibrillar MyopathiesReads 1 of these genesBAG3About this report →
- Inherited Neurodegenerative DisordersReads 5 of these genesTRIP4BSCL2CAPN1GARS1REEP1About this report →
- Hereditary Corneal DystrophiesReads 1 of these genesTCF4About this report →
- GPI Anchor Biosynthesis DefectsReads 1 of these genesPIGGAbout this report →
- Neonatal Diabetes MellitusReads 1 of these genesBSCL2About this report →
- Nephronophthisis and Senior-Løken SyndromeReads 1 of these genesWDR19About this report →
- Ehlers-Danlos SyndromeReads 1 of these genesCOL12A1About this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 1 of these genesSCN9AAbout this report →
- Noonan SyndromeReads 1 of these genesSPRED2About this report →
- Syndromic CraniosynostosisReads 1 of these genesWDR19About this report →
- Congenital Disorders of GlycosylationReads 2 of these genesRFT1PIGGAbout this report →
- Congenital Myasthenic SyndromeReads 1 of these genesSCN4AAbout this report →
- VitreoretinopathyReads 1 of these genesCOL9A3About this report →
- Diabetes MellitusReads 1 of these genesBSCL2About this report →
- Osteogenesis ImperfectaReads 1 of these genesKDELR2About this report →
- Retinitis PigmentosaReads 1 of these genesHK1About this report →
Pes valgus ile bağlantılı genleri ve genomunuzun geri kalanını tek bir testle okuyun.
$449'den başlayanÜcretsiz kargo · Sonuçlar 6–8 hafta içinde
Genome Test'imi alPes valgus ile ilişkili 64 gen
Bu genlerdeki değişiklikler, Pes valgus özelliğinin görüldüğü nadir durumlara yol açar. Bu özelliğe sahip çoğu kişide bu durumlardan hiçbiri yoktur; ayrıca bu listedeki bir gen, kimsenin kendi genomu hakkında bir şey söylemez.
| Gen | Ne sıklıkla görüldüğü | Durumlar |
|---|---|---|
| COL9A3collagen type IX alpha 3 chain | Her zaman | 1 durumda |
| COPZ1coat protein complex I subunit zeta 1 | Her zaman | 1 durumda |
| FBN1fibrillin 1 | Her zaman | 1 durumda |
| FDXRferredoxin reductase | Her zaman | 1 durumda |
| FEM1Bfem-1 homolog B | Her zaman | 1 durumda |
| GTF3C3general transcription factor IIIC subunit 3 | Her zaman | 1 durumda |
| LONP1lon peptidase 1, mitochondrial | Her zaman | 1 durumda |
| MED16mediator complex subunit 16 | Her zaman | 1 durumda |
| MYMXmyomixer, myoblast fusion factor | Her zaman | 1 durumda |
| NDC1NDC1 transmembrane nucleoporin | Her zaman | 1 durumda |
| RFT1RFT1 glycolipid translocator homolog | Her zaman | 1 durumda |
| TOR1Atorsin family 1 member A | Her zaman | 1 durumda |
| WDR19WD repeat domain 19 | Her zaman | 2 durumda |
| NSD1nuclear receptor binding SET domain protein 1 | Çok sık (%80–99) | 1 durumda |
| TCF4transcription factor 4 | Çok sık (%80–99) | 2 durumda |
| ANO1anoctamin 1 | Sık (%30–79) | 1 durumda |
| BAG3BAG cochaperone 3 | Sık (%30–79) | 1 durumda |
| COL12A1collagen type XII alpha 1 chain | Sık (%30–79) | 1 durumda |
| COL6A1collagen type VI alpha 1 chain | Sık (%30–79) | 1 durumda |
| COL6A2collagen type VI alpha 2 chain | Sık (%30–79) | 2 durumda |
| COL6A3collagen type VI alpha 3 chain | Sık (%30–79) | 1 durumda |
| FLNAfilamin A | Sık (%30–79) | 1 durumda |
| HNRNPRheterogeneous nuclear ribonucleoprotein R | Sık (%30–79) | 1 durumda |
| LARGE1LARGE xylosyl- and glucuronyltransferase 1 | Sık (%30–79) | 1 durumda |
| MAP3K7mitogen-activated protein kinase kinase kinase 7 | Sık (%30–79) | 1 durumda |
| MBD5methyl-CpG binding domain protein 5 | Sık (%30–79) | 1 durumda |
| PUF60poly(U) binding splicing factor 60 | Sık (%30–79) | 1 durumda |
| SLC16A2solute carrier family 16 member 2 | Sık (%30–79) | 1 durumda |
| SMG9SMG9 nonsense mediated mRNA decay factor | Sık (%30–79) | 1 durumda |
| TRIP4thyroid hormone receptor interactor 4 | Sık (%30–79) | 2 durumda |
| BSCL2BSCL2 lipid droplet biogenesis associated, seipin | Bazen (%5–29) | 1 durumda |
| CACNA1Ccalcium voltage-gated channel subunit alpha1 C | Bazen (%5–29) | 1 durumda |
| CAPN1calpain 1 | Bazen (%5–29) | 2 durumda |
| CDC42BPBCDC42 binding protein kinase beta | Bazen (%5–29) | 1 durumda |
| EBF3EBF transcription factor 3 | Bazen (%5–29) | 1 durumda |
| GABRA1gamma-aminobutyric acid type A receptor subunit alpha1 | Bazen (%5–29) | 1 durumda |
| GABRG2gamma-aminobutyric acid type A receptor subunit gamma2 | Bazen (%5–29) | 1 durumda |
| GARS1glycyl-tRNA synthetase 1 | Bazen (%5–29) | 1 durumda |
| GNB2G protein subunit beta 2 | Bazen (%5–29) | 1 durumda |
| H4C5H4 clustered histone 5 | Bazen (%5–29) | 1 durumda |
24 gen daha göster
| Gen | Ne sıklıkla görüldüğü | Durumlar |
|---|---|---|
| HK1hexokinase 1 | Bazen (%5–29) | 1 durumda |
| KDELR2KDEL endoplasmic reticulum protein retention receptor 2 | Bazen (%5–29) | 1 durumda |
| LRRC7leucine rich repeat containing 7 | Bazen (%5–29) | 1 durumda |
| MYPNmyopalladin | Bazen (%5–29) | 1 durumda |
| PCDH19protocadherin 19 | Bazen (%5–29) | 1 durumda |
| PIGGphosphatidylinositol glycan anchor biosynthesis class G (EMM blood group) | Bazen (%5–29) | 1 durumda |
| PPP1R15Bprotein phosphatase 1 regulatory subunit 15B | Bazen (%5–29) | 1 durumda |
| RAI1retinoic acid induced 1 | Bazen (%5–29) | 1 durumda |
| REEP1receptor accessory protein 1 | Bazen (%5–29) | 1 durumda |
| RNU2-2RNA, U2 small nuclear 2 | Bazen (%5–29) | 1 durumda |
| SCN1Asodium voltage-gated channel alpha subunit 1 | Bazen (%5–29) | 1 durumda |
| SCN1Bsodium voltage-gated channel beta subunit 1 | Bazen (%5–29) | 1 durumda |
| SCN2Asodium voltage-gated channel alpha subunit 2 | Bazen (%5–29) | 1 durumda |
| SCN4Asodium voltage-gated channel alpha subunit 4 | Bazen (%5–29) | 2 durumda |
| SCN9Asodium voltage-gated channel alpha subunit 9 | Bazen (%5–29) | 1 durumda |
| SMOC1SPARC related modular calcium binding 1 | Bazen (%5–29) | 1 durumda |
| SPRED2sprouty related EVH1 domain containing 2 | Bazen (%5–29) | 1 durumda |
| SYT1synaptotagmin 1 | Bazen (%5–29) | 1 durumda |
| TPM2tropomyosin 2 | Bazen (%5–29) | 1 durumda |
| TPM3tropomyosin 3 | Bazen (%5–29) | 1 durumda |
| TRMT10AtRNA methyltransferase 10A | Bazen (%5–29) | 1 durumda |
| WACWW domain containing adaptor with coiled-coil | Bazen (%5–29) | 1 durumda |
| SH3TC2SH3 domain and tetratricopeptide repeats 2 | Seyrek (%1–4) | 1 durumda |
| GDF5growth differentiation factor 5 | Kaydedilmedi | 1 durumda |
Bu özelliğin, genin ilişkili olduğu durumlardan birine sahip kişiler arasında ne sıklıkta görüldüğü; Human Phenotype Ontology'nin kaydettiği şekliyle, bunlar arasında en sık görülen oran. Bu sayfalar özellikleri ve bunların arkasındaki araştırmaları anlatır; tanı koymaz. Belirtiler hakkında bir doktora veya genetik danışmana başvurmanız gerekir.
Daha geniş özellikler
Bilgilerin kaynağı
- Human Phenotype Ontology, 2026-09-01 sürümü: özellik, adları, tanımı ve buna bağlı genler. Ayrıntılar için hpo.jax.org adresine bakın.
- Veri sürümü 2026.10.19-9814e911.
AtlasKimlere Yardımcı OluyoruzBilimimizÜrünlerSonuçlar
Giriş YapSorGenomunuzu dizileyin↗
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