AtlasTræk
Wide nasal base
Increased distance between the attachments of the alae nasi to the face.
Resumé
- Også kaldet
- Broad base of nose, Broad nasal base, Increased width of base of nose, Increased width of nasal base, Wide base of nose
- Kropssystem
- Abnormality of head or neck
AtlasDenne 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/wide-nasal-base.json"
page <- fromJSON(url)
page$trait$nameLæs de gener, der er knyttet til Wide nasal base, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test20 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.
- Coffin-Siris SyndromeReads 11 of these genesARID1AARID1BARID2DPF2SMARCA4SMARCB1About this report →
- Rhabdoid Tumour and SWI/SNF Tumour PredispositionReads 3 of these genesSMARCA4SMARCB1SMARCE1About this report →
- DOORS SyndromeReads 2 of these genesATP6V1B2TBC1D24About this report →
- Feingold Syndrome Type 1Reads 1 of these genesMYCNAbout this report →
Show 16 more reports
- Stüve-Wiedemann SyndromeReads 1 of these genesLIFRAbout this report →
- Intellectual DisabilityReads 10 of these genesMYT1LARID1AARID1BSMARCA4SMARCB1KMT5BAbout this report →
- Achondrogenesis panelReads 1 of these genesSLC26A2About this report →
- Complex Neurodevelopmental Disorder (TRRAP, MYH10, RERE, SOX11)Reads 1 of these genesSOX11About this report →
- NeurofibromatosisReads 1 of these genesSMARCB1About this report →
- Periventricular Nodular HeterotopiaReads 1 of these genesFLNAAbout this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 1 of these genesFLNAAbout this report →
- Epiphyseal and Spondyloepiphyseal DysplasiasReads 1 of these genesSLC26A2About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesFLNAAbout this report →
- Cutis LaxaReads 1 of these genesATP6V1E1About this report →
- Epilepsy (Full Panel)Reads 3 of these genesFLNAATP6V1B2TBC1D24About this report →
- Syndromic Complex Neurodevelopmental DisorderReads 1 of these genesMYT1LAbout this report →
- Male InfertilityReads 1 of these genesBCORL1About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesSNX14About this report →
- Hearing Loss and DeafnessReads 1 of these genesTBC1D24About this report →
- Inherited Neurodegenerative DisordersReads 1 of these genesSNX14About this report →
Læs de gener, der er knyttet til Wide nasal base, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test29 gener knyttet til Wide nasal base
Ændringer i disse gener forårsager sjældne tilstande, hvor Wide nasal base 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 |
|---|---|---|
| ATP6V1E1ATPase H+ transporting V1 subunit E1 | Altid | I 1 tilstand |
| EXOSC2exosome component 2 | Altid | I 1 tilstand |
| FLNAfilamin A | Altid | I 1 tilstand |
| LIFRLIF receptor subunit alpha | Altid | I 1 tilstand |
| MYCNMYCN proto-oncogene, bHLH transcription factor | Altid | I 1 tilstand |
| MYT1Lmyelin transcription factor 1 like | Altid | I 1 tilstand |
| ATP6V1B2ATPase H+ transporting V1 subunit B2 | Meget ofte (80–99 %) | I 1 tilstand |
| TBC1D24TBC1 domain family member 24 | Meget ofte (80–99 %) | I 1 tilstand |
| ARID1AAT-rich interaction domain 1A | Ofte (30–79 %) | I 1 tilstand |
| ARID1BAT-rich interaction domain 1B | Ofte (30–79 %) | I 1 tilstand |
| ARID2AT-rich interaction domain 2 | Ofte (30–79 %) | I 1 tilstand |
| DPF2double PHD fingers 2 | Ofte (30–79 %) | I 1 tilstand |
| SMARCA4SWI/SNF related BAF chromatin remodeling complex subunit ATPase 4 | Ofte (30–79 %) | I 1 tilstand |
| SMARCB1SWI/SNF related BAF chromatin remodeling complex subunit B1 | Ofte (30–79 %) | I 1 tilstand |
| SMARCC2SWI/SNF related BAF chromatin remodeling complex subunit C2 | Ofte (30–79 %) | I 1 tilstand |
| SMARCD1SWI/SNF related BAF chromatin remodeling complex subunit D1 | Ofte (30–79 %) | I 1 tilstand |
| SMARCE1SWI/SNF related BAF chromatin remodeling complex subunit E1 | Ofte (30–79 %) | I 1 tilstand |
| SOX11SRY-box transcription factor 11 | Ofte (30–79 %) | I 1 tilstand |
| SOX4SRY-box transcription factor 4 | Ofte (30–79 %) | I 1 tilstand |
| ABCA5ATP binding cassette subfamily A member 5 | Nogle gange (5–29 %) | I 1 tilstand |
| ATXN7L3ataxin 7 like 3 | Nogle gange (5–29 %) | I 1 tilstand |
| BCORL1BCL6 corepressor like 1 | Nogle gange (5–29 %) | I 1 tilstand |
| KMT5Blysine methyltransferase 5B | Nogle gange (5–29 %) | I 1 tilstand |
| SIN3ASIN3 transcription regulator family member A | Nogle gange (5–29 %) | I 1 tilstand |
| SLC26A2solute carrier family 26 member 2 | Nogle gange (5–29 %) | I 1 tilstand |
| SNX14sorting nexin 14 | Nogle gange (5–29 %) | I 2 tilstande |
| USP9Xubiquitin specific peptidase 9 X-linked | Nogle gange (5–29 %) | I 1 tilstand |
| CTCFCCCTC-binding factor | Sjældent (1–4%) | I 1 tilstand |
| SMARCA2SWI/SNF related BAF chromatin remodeling complex subunit ATPase 2 | 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 2026.10.19-9814e911.
AtlasFrom 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.
Gratis forsendelse · Resultater på 6–8 uger
