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Træk
Absent eyelashes
Lack of eyelashes.
Resumé
- Også kaldet
- Failure of development of eyelashes, Atrichia of eyelashes
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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/absent-eyelashes.json"
page <- fromJSON(url)
page$trait$nameAbsent eyelashesHP:0000561
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Læs de gener, der er knyttet til Absent eyelashes, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test37 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.
- Treacher Collins SyndromeReads 4 of these genesTCOF1POLR1BPOLR1CPOLR1DAbout this report →
- Ectodermal DysplasiasReads 5 of these genesEDARADDHOXC13KRT85EDATP63About this report →
- Rothmund-Thomson SyndromeReads 2 of these genesANAPC1RECQL4About this report →
- CWC27-Related Retinitis Pigmentosa with Skeletal AnomaliesReads 1 of these genesCWC27About this report →
Show 33 more reports
- IFAP Syndrome (MBTPS2)Reads 1 of these genesMBTPS2About this report →
- POLR1C-Related DisorderReads 1 of these genesPOLR1CAbout this report →
- POLR3A-Related DisorderReads 1 of these genesPOLR3AAbout this report →
- Restrictive Dermopathy (ZMPSTE24)Reads 1 of these genesZMPSTE24About this report →
- Noonan SyndromeReads 4 of these genesBRAFKRASMAP2K1MAP2K2About this report →
- Epidermolysis BullosaReads 3 of these genesPKP1DSPJUPAbout this report →
- Arrhythmogenic CardiomyopathyReads 2 of these genesDSPJUPAbout this report →
- LipodystrophyReads 2 of these genesLMNAZMPSTE24About this report →
- Fraser SyndromeReads 1 of these genesFRAS1About this report →
- Van der Woude and Popliteal Pterygium Syndromes (IRF6)Reads 1 of these genesRIPK4About this report →
- Severe Combined ImmunodeficiencyReads 3 of these genesDCLRE1CRAG1RAG2About this report →
- Hypertrophic CardiomyopathyReads 4 of these genesBRAFKRASMAP2K1MAP2K2About this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 3 of these genesDSPGJB2MBTPS2About this report →
- Syndromic CraniosynostosisReads 2 of these genesRNU12RECQL4About this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 2 of these genesPOLR1CPOLR3AAbout this report →
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 1 of these genesKRASAbout this report →
- Hypodontia and AnodontiaReads 1 of these genesEDAAbout this report →
- Disorders of Glycine & Serine MetabolismReads 1 of these genesPHGDHAbout this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesLMNAAbout this report →
- Osteogenesis ImperfectaReads 2 of these genesPOLR3AMBTPS2About this report →
- Other Inborn Errors of ImmunityReads 4 of these genesDCLRE1CRAG1RAG2KRASAbout this report →
- Hereditary Hypotrichosis, Woolly Hair and MonilethrixReads 1 of these genesHRAbout this report →
- Primary Lymphoedema & Lymphatic MalformationsReads 1 of these genesSOX18About this report →
- Other Inherited LeukodystrophiesReads 2 of these genesPOLR1CPOLR3AAbout this report →
- Autoimmune DiseaseReads 1 of these genesKRASAbout this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesLMNAAbout this report →
- DNA Repair DiseaseReads 1 of these genesDCLRE1CAbout this report →
- Dilated CardiomyopathyReads 1 of these genesLMNAAbout this report →
- Female InfertilityReads 1 of these genesTP63About this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesLMNAAbout this report →
- Inherited Neurodegenerative DisordersReads 2 of these genesPOLR1CPOLR3AAbout this report →
- Hearing Loss and DeafnessReads 1 of these genesGJB2About this report →
- Rare Hereditary Peripheral NeuropathiesReads 1 of these genesLMNAAbout this report →
Læs de gener, der er knyttet til Absent eyelashes, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test37 gener knyttet til Absent eyelashes
Ændringer i disse gener forårsager sjældne tilstande, hvor Absent eyelashes 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 |
|---|---|---|
| DCLRE1CDNA cross-link repair 1C | Altid | I 1 tilstand |
| EDARADDEDAR associated via death domain | Altid | I 1 tilstand |
| HOXC13homeobox C13 | Altid | I 1 tilstand |
| HRHR lysine demethylase and nuclear receptor corepressor | Altid | I 2 tilstande |
| KRT85keratin 85 | Altid | I 1 tilstand |
| LRP1LDL receptor related protein 1 | Altid | I 1 tilstand |
| PKP1plakophilin 1 | Altid | I 1 tilstand |
| RAG1recombination activating 1 | Altid | I 1 tilstand |
| RAG2recombination activating 2 | Altid | I 1 tilstand |
| SOX18SRY-box transcription factor 18 | Altid | I 3 tilstande |
| TCOF1treacle ribosome biogenesis factor 1 | Altid | I 2 tilstande |
| LMNAlamin A/C | Meget ofte (80–99 %) | I 2 tilstande |
| RNU12RNA, U12 small nuclear | Meget ofte (80–99 %) | I 1 tilstand |
| TWIST2twist family bHLH transcription factor 2 | Meget ofte (80–99 %) | I 2 tilstande |
| ANAPC1anaphase promoting complex subunit 1 | Ofte (30–79 %) | I 1 tilstand |
| DSPdesmoplakin | Ofte (30–79 %) | I 1 tilstand |
| FGF10fibroblast growth factor 10 | Ofte (30–79 %) | I 1 tilstand |
| JUPjunction plakoglobin | Ofte (30–79 %) | I 1 tilstand |
| POLR1BRNA polymerase I subunit B | Ofte (30–79 %) | I 1 tilstand |
| POLR1CRNA polymerase I and III subunit C | Ofte (30–79 %) | I 1 tilstand |
| POLR1DRNA polymerase I and III subunit D | Ofte (30–79 %) | I 1 tilstand |
| POLR3ARNA polymerase III subunit A | Ofte (30–79 %) | I 1 tilstand |
| RECQL4RecQ like helicase 4 | Ofte (30–79 %) | I 1 tilstand |
| CWC27CWC27 spliceosome associated cyclophilin | Nogle gange (5–29 %) | I 2 tilstande |
| ODC1ornithine decarboxylase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Ikke registreret | I 1 tilstand |
| EDAectodysplasin A | Ikke registreret | I 1 tilstand |
| FRAS1Fraser extracellular matrix complex subunit 1 | Ikke registreret | I 1 tilstand |
| GJB2gap junction protein beta 2 | Ikke registreret | I 1 tilstand |
| KRASKRas proto-oncogene, GTPase | Ikke registreret | I 1 tilstand |
| MAP2K1mitogen-activated protein kinase kinase 1 | Ikke registreret | I 1 tilstand |
| MAP2K2mitogen-activated protein kinase kinase 2 | Ikke registreret | I 1 tilstand |
| MBTPS2membrane bound transcription factor peptidase, site 2 | Ikke registreret | I 1 tilstand |
| PHGDHphosphoglycerate dehydrogenase | Ikke registreret | I 1 tilstand |
| RIPK4receptor interacting serine/threonine kinase 4 | Ikke registreret | I 1 tilstand |
| TP63tumor protein p63 | Ikke registreret | I 1 tilstand |
| ZMPSTE24zinc metallopeptidase STE24 | 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.
Snævrere træk
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.
AtlasHvem vi hjælperVores videnskabProdukterResultater
Log indSpørgSekvenér dit genom↗
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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