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Talipes valgus
Outward turning of the heel, resulting in clubfoot with the person walking on the inner part of the foot.
Resumé
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library(jsonlite)
url <- "https://dantelabs.com/traits/talipes-valgus.json"
page <- fromJSON(url)
page$trait$nameLæs de gener, der er knyttet til Talipes valgus, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test19 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.
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- Epilepsy (Full Panel)Reads 10 of these genesFGF13GABRG2HCN1PRRT2SCN1ASCN1BAbout this report →
Show 15 more reports
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- Usher SyndromeReads 1 of these genesADGRV1About this report →
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Læs de gener, der er knyttet til Talipes valgus, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test23 gener knyttet til Talipes valgus
Ændringer i disse gener forårsager sjældne tilstande, hvor Talipes valgus 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 |
|---|---|---|
| DNMT3ADNA methyltransferase 3 alpha | Altid | I 1 tilstand |
| HNRNPH1heterogeneous nuclear ribonucleoprotein H1 | Altid | I 1 tilstand |
| RAB3GAP2RAB3 GTPase activating non-catalytic protein subunit 2 | Altid | I 1 tilstand |
| CARS1cysteinyl-tRNA synthetase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| CHMP1Acharged multivesicular body protein 1A | Nogle gange (5–29 %) | I 1 tilstand |
| MAN2B1mannosidase alpha class 2B member 1 | Nogle gange (5–29 %) | I 1 tilstand |
| NONOnon-POU domain containing octamer binding | Nogle gange (5–29 %) | I 1 tilstand |
| ADGRV1adhesion G protein-coupled receptor V1 | Sjældent (1–4%) | I 1 tilstand |
| CPA6carboxypeptidase A6 | Sjældent (1–4%) | I 1 tilstand |
| EXT1exostosin glycosyltransferase 1 | Sjældent (1–4%) | I 1 tilstand |
| EXT2exostosin glycosyltransferase 2 | Sjældent (1–4%) | I 1 tilstand |
| FGF13fibroblast growth factor 13 | Sjældent (1–4%) | I 1 tilstand |
| GABRDgamma-aminobutyric acid type A receptor subunit delta | Sjældent (1–4%) | I 1 tilstand |
| GABRG2gamma-aminobutyric acid type A receptor subunit gamma2 | Sjældent (1–4%) | I 1 tilstand |
| HCN1hyperpolarization activated cyclic nucleotide gated potassium channel 1 | Sjældent (1–4%) | I 1 tilstand |
| PRRT2proline rich transmembrane protein 2 | Sjældent (1–4%) | I 1 tilstand |
| SCN1Asodium voltage-gated channel alpha subunit 1 | Sjældent (1–4%) | I 1 tilstand |
| SCN1Bsodium voltage-gated channel beta subunit 1 | Sjældent (1–4%) | I 1 tilstand |
| SCN2Asodium voltage-gated channel alpha subunit 2 | Sjældent (1–4%) | I 1 tilstand |
| SCN9Asodium voltage-gated channel alpha subunit 9 | Sjældent (1–4%) | I 1 tilstand |
| SLC32A1solute carrier family 32 member 1 | Sjældent (1–4%) | I 1 tilstand |
| STX1Bsyntaxin 1B | Sjældent (1–4%) | I 1 tilstand |
| LIFRLIF receptor subunit alpha | 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.
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 2026.10.21-777c9289.
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Gratis forsendelse · Resultater på 6–8 uger
