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Træk
Webbed neck
Pterygium colli is a congenital skin fold that runs along the sides of the neck down to the shoulders. It involves an ectopic fibrotic facial band superficial to the trapezius muscle. Excess hair-bearing skin is also present and extends down the cervical region well beyond the normal hairline.
Resumé
- Også kaldet
- Neck webbing, Pterygium colli
- Kropssystem
- Abnormality of head or neck
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Denne side som data
Tilføj .json til sidens adresse, eller bed om application/json, for at læse den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/webbed-neck.json"
page <- fromJSON(url)
page$trait$nameWebbed neckHP:0000465
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Læs de gener, der er knyttet til Webbed neck, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test50 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.
- Noonan SyndromeReads 20 of these genesBRAFSOS2SPRED2CBLKRASLZTR1About this report →
- Diamond-Blackfan AnemiaReads 14 of these genesGATA1HEATR3RPL11RPL15RPL26RPL35AAbout this report →
- Hypertrophic CardiomyopathyReads 21 of these genesBRAFSOS2SPRED2KRASLZTR1MAP2K2About this report →
- NeurofibromatosisReads 2 of these genesLZTR1NF1About this report →
Show 46 more reports
- CHARGE SyndromeReads 1 of these genesCHD7About this report →
- Deficiency of Adenosine Deaminase 2 (DADA2)Reads 1 of these genesADA2About this report →
- Hereditary RetinoblastomaReads 1 of these genesRB1About this report →
- Congenital Cranial Dysinnervation DisordersReads 2 of these genesCHN1MAFBAbout this report →
- Hereditary Gingival FibromatosisReads 1 of these genesSOS1About this report →
- Malignant Hyperthermia SusceptibilityReads 1 of these genesRYR1About this report →
- Inherited ThrombocytopeniasReads 4 of these genesACTBCDC42FLI1GATA1About this report →
- LipodystrophyReads 2 of these genesLMNAZMPSTE24About this report →
- Congenital Diaphragmatic Hernia (Monogenic)Reads 1 of these genesALDH1A2About this report →
- Primary Lymphoedema & Lymphatic MalformationsReads 2 of these genesFOXC2PIEZO1About this report →
- 46,XX Differences of Sex DevelopmentReads 1 of these genesSRYAbout this report →
- Inherited Predisposition to Myeloid Blood CancersReads 1 of these genesGATA2About this report →
- Congenital MyopathiesReads 2 of these genesTPM2RYR1About this report →
- Autoimmune DiseaseReads 2 of these genesCHRNGKRASAbout this report →
- Ehlers-Danlos SyndromeReads 2 of these genesSLC39A13AEBP1About this report →
- Growth Hormone Insensitivity & IGF-1 Axis DisordersReads 1 of these genesIGF1RAbout this report →
- Congenital Disorders of GlycosylationReads 4 of these genesB3GAT3B3GLCTPIGLSLC35A1About this report →
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 1 of these genesKRASAbout this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesLMNAAbout this report →
- Red Blood Cell Membrane DisordersReads 1 of these genesPIEZO1About this report →
- Intellectual DisabilityReads 5 of these genesSMSANKRD11NAA10NSD2PIGLAbout this report →
- Meckel SyndromeReads 1 of these genesMKS1About this report →
- Dilated CardiomyopathyReads 2 of these genesRAF1LMNAAbout this report →
- Myofibrillar MyopathiesReads 1 of these genesRYR1About this report →
- OsteopetrosisReads 1 of these genesAMER1About this report →
- Fanconi AnemiaReads 1 of these genesFANCLAbout this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 1 of these genesSRYAbout this report →
- Congenital HypothyroidismReads 1 of these genesNKX2-1About this report →
- GPI Anchor Biosynthesis DefectsReads 1 of these genesPIGLAbout this report →
- Bardet-Biedl and Alström SyndromesReads 1 of these genesMKS1About this report →
- Syndromic CraniosynostosisReads 1 of these genesMEGF8About this report →
- VitreoretinopathyReads 1 of these genesXYLT2About this report →
- Microphthalmia, Anophthalmia & ColobomaReads 1 of these genesBCORAbout this report →
- Nephrotic SyndromeReads 1 of these genesLAMA5About this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesLMNAAbout this report →
- Osteogenesis ImperfectaReads 1 of these genesXYLT2About this report →
- Rare Monogenic Autoinflammatory DiseasesReads 1 of these genesADA2About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesACTBAbout this report →
- Joubert Syndrome And Related DisordersReads 1 of these genesMKS1About this report →
- DNA Repair DiseaseReads 1 of these genesFANCLAbout this report →
- Epilepsy (Full Panel)Reads 2 of these genesCPLX1STXBP1About this report →
- Hypogonadotropic HypogonadismReads 1 of these genesCHD7About this report →
- Other Inborn Errors of ImmunityReads 2 of these genesKRASGATA2About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesMKS1About this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesLMNAAbout this report →
- Hearing Loss and DeafnessReads 1 of these genesACTG1About this report →
Læs de gener, der er knyttet til Webbed neck, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test128 gener knyttet til Webbed neck
Ændringer i disse gener forårsager sjældne tilstande, hvor Webbed neck 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 |
|---|---|---|
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Altid | I 7 tilstande |
| ERI1exoribonuclease 1 | Altid | I 1 tilstand |
| HYAL2hyaluronidase 2 | Altid | I 1 tilstand |
| MYO18Bmyosin XVIIIB | Altid | I 1 tilstand |
| RC3H1ring finger and CCCH-type domains 1 | Altid | I 1 tilstand |
| SLC39A13solute carrier family 39 member 13 | Altid | I 1 tilstand |
| SMSspermine synthase | Altid | I 2 tilstande |
| SOS2SOS Ras/Rho guanine nucleotide exchange factor 2 | Altid | I 2 tilstande |
| SPRED2sprouty related EVH1 domain containing 2 | Altid | I 2 tilstande |
| CBLCbl proto-oncogene | Meget ofte (80–99 %) | I 2 tilstande |
| CHRNGcholinergic receptor nicotinic gamma subunit | Meget ofte (80–99 %) | I 1 tilstand |
| GDF3growth differentiation factor 3 | Meget ofte (80–99 %) | I 1 tilstand |
| GDF6growth differentiation factor 6 | Meget ofte (80–99 %) | I 2 tilstande |
| KRASKRas proto-oncogene, GTPase | Meget ofte (80–99 %) | I 4 tilstande |
| LZTR1leucine zipper like post translational regulator 1 | Meget ofte (80–99 %) | I 3 tilstande |
| MAP2K2mitogen-activated protein kinase kinase 2 | Meget ofte (80–99 %) | I 3 tilstande |
| MEOX1mesenchyme homeobox 1 | Meget ofte (80–99 %) | I 1 tilstand |
| MRASmuscle RAS oncogene homolog | Meget ofte (80–99 %) | I 1 tilstand |
| MYH3myosin heavy chain 3 | Meget ofte (80–99 %) | I 4 tilstande |
| NALCNsodium leak channel, non-selective | Meget ofte (80–99 %) | I 1 tilstand |
| NF1neurofibromin 1 | Meget ofte (80–99 %) | I 4 tilstande |
| NRASNRAS proto-oncogene, GTPase | Meget ofte (80–99 %) | I 2 tilstande |
| PPP1CBprotein phosphatase 1 catalytic subunit beta | Meget ofte (80–99 %) | I 2 tilstande |
| PTPN11protein tyrosine phosphatase non-receptor type 11 | Meget ofte (80–99 %) | I 4 tilstande |
| RAF1Raf-1 proto-oncogene, serine/threonine kinase | Meget ofte (80–99 %) | I 4 tilstande |
| RASA2RAS p21 protein activator 2 | Meget ofte (80–99 %) | I 1 tilstand |
| RIT1Ras like without CAAX 1 | Meget ofte (80–99 %) | I 2 tilstande |
| RRASRAS related | Meget ofte (80–99 %) | I 1 tilstand |
| RRAS2RAS related 2 | Meget ofte (80–99 %) | I 1 tilstand |
| SHOC2SHOC2 leucine rich repeat scaffold protein | Meget ofte (80–99 %) | I 2 tilstande |
| SOS1SOS Ras/Rac guanine nucleotide exchange factor 1 | Meget ofte (80–99 %) | I 2 tilstande |
| TNNI2troponin I2, fast skeletal type | Meget ofte (80–99 %) | I 2 tilstande |
| TNNT3troponin T3, fast skeletal type | Meget ofte (80–99 %) | I 1 tilstand |
| TPM2tropomyosin 2 | Meget ofte (80–99 %) | I 2 tilstande |
| AEBP1AE binding protein 1 | Ofte (30–79 %) | I 2 tilstande |
| ALDH1A2aldehyde dehydrogenase 1 family member A2 | Ofte (30–79 %) | I 1 tilstand |
| ALPK3alpha kinase 3 | Ofte (30–79 %) | I 1 tilstand |
| ANKRD11ankyrin repeat domain 11 | Ofte (30–79 %) | I 2 tilstande |
| B3GAT3beta-1,3-glucuronyltransferase 3 | Ofte (30–79 %) | I 1 tilstand |
| B3GLCTbeta 3-glucosyltransferase | Ofte (30–79 %) | I 2 tilstande |
Vis 88 gener mere
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| C2CD3C2 domain containing 3 centriole elongation regulator | Ofte (30–79 %) | I 1 tilstand |
| CHST3carbohydrate sulfotransferase 3 | Ofte (30–79 %) | I 1 tilstand |
| FANCLFA complementation group L | Ofte (30–79 %) | I 1 tilstand |
| FILIP1filamin A interacting protein 1 | Ofte (30–79 %) | I 1 tilstand |
| GLE1GLE1 RNA export mediator | Ofte (30–79 %) | I 1 tilstand |
| GPC3glypican 3 | Ofte (30–79 %) | I 1 tilstand |
| GPC4glypican 4 | Ofte (30–79 %) | I 1 tilstand |
| LAMA5laminin subunit alpha 5 | Ofte (30–79 %) | I 1 tilstand |
| MAP2K1mitogen-activated protein kinase kinase 1 | Ofte (30–79 %) | I 4 tilstande |
| MAPK1mitogen-activated protein kinase 1 | Ofte (30–79 %) | I 1 tilstand |
| MSL2MSL complex subunit 2 | Ofte (30–79 %) | I 1 tilstand |
| RYR1ryanodine receptor 1 | Ofte (30–79 %) | I 1 tilstand |
| TASP1taspase 1 | Ofte (30–79 %) | I 1 tilstand |
| XYLT2xylosyltransferase 2 | Ofte (30–79 %) | I 2 tilstande |
| ACTBactin beta | Nogle gange (5–29 %) | I 1 tilstand |
| ACTG1actin gamma 1 | Nogle gange (5–29 %) | I 2 tilstande |
| ADA2adenosine deaminase 2 | Nogle gange (5–29 %) | I 1 tilstand |
| BCORBCL6 corepressor | Nogle gange (5–29 %) | I 2 tilstande |
| CDC42cell division cycle 42 | Nogle gange (5–29 %) | I 2 tilstande |
| CHN1chimerin 1 | Nogle gange (5–29 %) | I 1 tilstand |
| CPLX1complexin 1 | Nogle gange (5–29 %) | I 1 tilstand |
| CTBP1C-terminal binding protein 1 | Nogle gange (5–29 %) | I 1 tilstand |
| DVL3dishevelled segment polarity protein 3 | Nogle gange (5–29 %) | I 1 tilstand |
| EFNB1ephrin B1 | Nogle gange (5–29 %) | I 1 tilstand |
| FBXO22F-box protein 22 | Nogle gange (5–29 %) | I 1 tilstand |
| FBXW11F-box and WD repeat domain containing 11 | Nogle gange (5–29 %) | I 1 tilstand |
| FGFRL1fibroblast growth factor receptor like 1 | Nogle gange (5–29 %) | I 1 tilstand |
| FLI1Fli-1 proto-oncogene, ETS transcription factor | Nogle gange (5–29 %) | I 1 tilstand |
| FOXC2forkhead box C2 | Nogle gange (5–29 %) | I 2 tilstande |
| GATA1GATA binding protein 1 | Nogle gange (5–29 %) | I 1 tilstand |
| GATA2GATA binding protein 2 | Nogle gange (5–29 %) | I 1 tilstand |
| HEATR3HEAT repeat containing 3 | Nogle gange (5–29 %) | I 1 tilstand |
| KMT2Alysine methyltransferase 2A | Nogle gange (5–29 %) | I 1 tilstand |
| LETM1leucine zipper and EF-hand containing transmembrane protein 1 | Nogle gange (5–29 %) | I 1 tilstand |
| LMNAlamin A/C | Nogle gange (5–29 %) | I 1 tilstand |
| LMX1BLIM homeobox transcription factor 1 beta | Nogle gange (5–29 %) | I 1 tilstand |
| MAFBMAF bZIP transcription factor B | Nogle gange (5–29 %) | I 1 tilstand |
| MAP3K7mitogen-activated protein kinase kinase kinase 7 | Nogle gange (5–29 %) | I 1 tilstand |
| MEGF8multiple EGF like domains 8 | Nogle gange (5–29 %) | I 1 tilstand |
| NAA10N-alpha-acetyltransferase 10, NatA catalytic subunit | Nogle gange (5–29 %) | I 2 tilstande |
| NSD2nuclear receptor binding SET domain protein 2 | Nogle gange (5–29 %) | I 1 tilstand |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Nogle gange (5–29 %) | I 1 tilstand |
| RB1RB transcriptional corepressor 1 | Nogle gange (5–29 %) | I 1 tilstand |
| RPL11ribosomal protein L11 | Nogle gange (5–29 %) | I 1 tilstand |
| RPL15ribosomal protein L15 | Nogle gange (5–29 %) | I 1 tilstand |
| RPL18ribosomal protein L18 | Nogle gange (5–29 %) | I 1 tilstand |
| RPL26ribosomal protein L26 | Nogle gange (5–29 %) | I 1 tilstand |
| RPL27ribosomal protein L27 | Nogle gange (5–29 %) | I 1 tilstand |
| RPL31ribosomal protein L31 | Nogle gange (5–29 %) | I 1 tilstand |
| RPL35ribosomal protein L35 | Nogle gange (5–29 %) | I 1 tilstand |
| RPL35Aribosomal protein L35a | Nogle gange (5–29 %) | I 1 tilstand |
| RPL5ribosomal protein L5 | Nogle gange (5–29 %) | I 1 tilstand |
| RPL8ribosomal protein L8 | Nogle gange (5–29 %) | I 1 tilstand |
| RPL9ribosomal protein L9 | Nogle gange (5–29 %) | I 1 tilstand |
| RPS10ribosomal protein S10 | Nogle gange (5–29 %) | I 2 tilstande |
| RPS15Aribosomal protein S15a | Nogle gange (5–29 %) | I 1 tilstand |
| RPS17ribosomal protein S17 | Nogle gange (5–29 %) | I 1 tilstand |
| RPS19ribosomal protein S19 | Nogle gange (5–29 %) | I 2 tilstande |
| RPS20ribosomal protein S20 | Nogle gange (5–29 %) | I 1 tilstand |
| RPS24ribosomal protein S24 | Nogle gange (5–29 %) | I 2 tilstande |
| RPS26ribosomal protein S26 | Nogle gange (5–29 %) | I 1 tilstand |
| RPS27ribosomal protein S27 | Nogle gange (5–29 %) | I 1 tilstand |
| RPS28ribosomal protein S28 | Nogle gange (5–29 %) | I 1 tilstand |
| RPS29ribosomal protein S29 | Nogle gange (5–29 %) | I 1 tilstand |
| RPS7ribosomal protein S7 | Nogle gange (5–29 %) | I 1 tilstand |
| SALL4spalt like transcription factor 4 | Nogle gange (5–29 %) | I 1 tilstand |
| SNRPBsmall nuclear ribonucleoprotein polypeptides B and B1 | Nogle gange (5–29 %) | I 2 tilstande |
| SRYsex determining region Y | Nogle gange (5–29 %) | I 1 tilstand |
| STXBP1syntaxin binding protein 1 | Nogle gange (5–29 %) | I 1 tilstand |
| TBX2T-box transcription factor 2 | Nogle gange (5–29 %) | I 1 tilstand |
| TMEM260transmembrane protein 260 | Nogle gange (5–29 %) | I 1 tilstand |
| TMEM94transmembrane protein 94 | Nogle gange (5–29 %) | I 1 tilstand |
| TSR2TSR2 ribosome maturation factor | Nogle gange (5–29 %) | I 1 tilstand |
| WBP11WW domain binding protein 11 | Nogle gange (5–29 %) | I 1 tilstand |
| ZMPSTE24zinc metallopeptidase STE24 | Nogle gange (5–29 %) | I 1 tilstand |
| CHD7chromodomain helicase DNA binding protein 7 | Sjældent (1–4%) | I 2 tilstande |
| NKX2-1NK2 homeobox 1 | Sjældent (1–4%) | I 1 tilstand |
| SEMA3Esemaphorin 3E | Sjældent (1–4%) | I 1 tilstand |
| AMER1APC membrane recruitment protein 1 | Ikke registreret | I 1 tilstand |
| BLTP1bridge-like lipid transfer protein family member 1 | Ikke registreret | I 1 tilstand |
| BMPERBMP binding endothelial regulator | Ikke registreret | I 1 tilstand |
| HRASHRas proto-oncogene, GTPase | Ikke registreret | I 1 tilstand |
| IGF1Rinsulin like growth factor 1 receptor | Ikke registreret | I 1 tilstand |
| MKS1MKS transition zone complex subunit 1 | Ikke registreret | I 1 tilstand |
| PIEZO1piezo type mechanosensitive ion channel component 1 (Er blood group) | Ikke registreret | I 1 tilstand |
| PIGLphosphatidylinositol glycan anchor biosynthesis class L | Ikke registreret | I 1 tilstand |
| SLC35A1solute carrier family 35 member A1 | Ikke registreret | I 1 tilstand |
| TAPT1transmembrane anterior posterior transformation 1 | 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 2026.10.18-8b139e39.
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