AtlasKellele me abiks olemeMeie teadusTootedTulemused
Logi sisseKüsiSekveneeri oma genoom↗
Tunnus
Absent eyebrow
Absence of the eyebrow.
Kokkuvõte
- Teised nimetused
- Failure of development of eyebrows, Loss of eyebrows, Missing eyebrows, Absent eyebrows
AtlasKellele me abiks olemeMeie teadusTootedTulemused
Logi sisseKüsiSekveneeri oma genoom↗
Selle lehe andmed
Lehe aadressile saab lisada .json või päringusse application/json, et lugeda seda JSON-vormingus.
library(jsonlite)
url <- "https://dantelabs.com/traits/absent-eyebrow.json"
page <- fromJSON(url)
page$trait$nameAbsent eyebrowHP:0002223
AtlasKellele me abiks olemeMeie teadusTootedTulemused
Logi sisseKüsiSekveneeri oma genoom↗
Lugege välja geenid, mis on seotud Absent eyebrow-ga, ja kogu ülejäänud genoom ühe testiga.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test40 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.
- Ectodermal DysplasiasReads 5 of these genesEDAEDARADDHOXC13KRT85GJB6About this report →
- Rothmund-Thomson SyndromeReads 2 of these genesANAPC1RECQL4About this report →
- CWC27-Related Retinitis Pigmentosa with Skeletal AnomaliesReads 1 of these genesCWC27About this report →
- Frontonasal Dysplasia 3 (ALX1)Reads 1 of these genesALX1About this report →
Show 36 more reports
- IFAP Syndrome (MBTPS2)Reads 1 of these genesMBTPS2About this report →
- Kaufman Oculocerebrofacial SyndromeReads 1 of these genesUBE3BAbout 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 →
- Congenital Intestinal Atresia & Short BowelReads 1 of these genesTTC7AAbout this report →
- Epidermolysis BullosaReads 3 of these genesPKP1DSPJUPAbout this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 4 of these genesDSPMBTPS2GJA1GJB6About 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 Hypotrichosis, Woolly Hair and MonilethrixReads 2 of these genesHRCDH3About this report →
- Syndromic CraniosynostosisReads 2 of these genesRNU12RECQL4About this report →
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 1 of these genesKRASAbout this report →
- Colorectal Cancer & PolyposisReads 1 of these genesAXIN2About this report →
- Hyper-IgE SyndromeReads 1 of these genesSPINK5About this report →
- Hypodontia and AnodontiaReads 1 of these genesEDAAbout this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesLMNAAbout this report →
- Osteogenesis ImperfectaReads 2 of these genesMBTPS2POLR3AAbout this report →
- Other Inborn Errors of ImmunityReads 5 of these genesDCLRE1CRAG1RAG2SPINK5KRASAbout this report →
- PorphyriaReads 1 of these genesUROSAbout this report →
- Primary Lymphoedema & Lymphatic MalformationsReads 1 of these genesSOX18About this report →
- Autoimmune DiseaseReads 1 of these genesKRASAbout this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 1 of these genesPOLR3AAbout 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 →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesLMNAAbout this report →
- Other Inherited LeukodystrophiesReads 1 of these genesPOLR3AAbout this report →
- Hearing Loss and DeafnessReads 1 of these genesGJB6About this report →
- Rare Hereditary Peripheral NeuropathiesReads 1 of these genesLMNAAbout this report →
- Intellectual DisabilityReads 1 of these genesSMARCA2About this report →
- Inherited Neurodegenerative DisordersReads 1 of these genesPOLR3AAbout this report →
Lugege välja geenid, mis on seotud Absent eyebrow-ga, ja kogu ülejäänud genoom ühe testiga.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test40 geeni on seotud tunnusega Absent eyebrow
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Absent eyebrow. Enamikul selle tunnusega inimestest ei ole ühtegi neist haigustest. Selles loendis olev geen ei ütle midagi kellegi enda genoomi kohta.
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| ALX1ALX homeobox 1 | Alati | Esineb 1 haiguses |
| DCLRE1CDNA cross-link repair 1C | Alati | Esineb 1 haiguses |
| EDAectodysplasin A | Alati | Esineb 1 haiguses |
| EDARADDEDAR associated via death domain | Alati | Esineb 1 haiguses |
| HOXC13homeobox C13 | Alati | Esineb 1 haiguses |
| HRHR lysine demethylase and nuclear receptor corepressor | Alati | Esineb 2 haiguses |
| KRT85keratin 85 | Alati | Esineb 1 haiguses |
| ODC1ornithine decarboxylase 1 | Alati | Esineb 2 haiguses |
| PKP1plakophilin 1 | Alati | Esineb 1 haiguses |
| RAG1recombination activating 1 | Alati | Esineb 1 haiguses |
| RAG2recombination activating 2 | Alati | Esineb 1 haiguses |
| SOX18SRY-box transcription factor 18 | Alati | Esineb 3 haiguses |
| SPINK5serine peptidase inhibitor Kazal type 5 | Alati | Esineb 1 haiguses |
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Väga sageli (80–99%) | Esineb 1 haiguses |
| KRASKRas proto-oncogene, GTPase | Väga sageli (80–99%) | Esineb 2 haiguses |
| LMNAlamin A/C | Väga sageli (80–99%) | Esineb 2 haiguses |
| MAP2K1mitogen-activated protein kinase kinase 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| MAP2K2mitogen-activated protein kinase kinase 2 | Väga sageli (80–99%) | Esineb 2 haiguses |
| RNU12RNA, U12 small nuclear | Väga sageli (80–99%) | Esineb 1 haiguses |
| TWIST2twist family bHLH transcription factor 2 | Väga sageli (80–99%) | Esineb 2 haiguses |
| ANAPC1anaphase promoting complex subunit 1 | Sageli (30–79%) | Esineb 1 haiguses |
| AXIN2axin 2 | Sageli (30–79%) | Esineb 1 haiguses |
| CDH3cadherin 3 | Sageli (30–79%) | Esineb 1 haiguses |
| DSPdesmoplakin | Sageli (30–79%) | Esineb 1 haiguses |
| JUPjunction plakoglobin | Sageli (30–79%) | Esineb 1 haiguses |
| LTV1LTV1 ribosome biogenesis factor | Sageli (30–79%) | Esineb 1 haiguses |
| MBTPS2membrane bound transcription factor peptidase, site 2 | Sageli (30–79%) | Esineb 2 haiguses |
| PI4KAphosphatidylinositol 4-kinase alpha | Sageli (30–79%) | Esineb 1 haiguses |
| POLR3ARNA polymerase III subunit A | Sageli (30–79%) | Esineb 1 haiguses |
| RECQL4RecQ like helicase 4 | Sageli (30–79%) | Esineb 1 haiguses |
| TTC7Atetratricopeptide repeat domain 7A | Sageli (30–79%) | Esineb 1 haiguses |
| UBE3Bubiquitin protein ligase E3B | Sageli (30–79%) | Esineb 1 haiguses |
| CWC27CWC27 spliceosome associated cyclophilin | Mõnikord (5–29%) | Esineb 2 haiguses |
| GJA1gap junction protein alpha 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GJB6gap junction protein beta 6 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ZMPSTE24zinc metallopeptidase STE24 | Mõnikord (5–29%) | Esineb 1 haiguses |
| FRAS1Fraser extracellular matrix complex subunit 1 | Pole registreeritud | Esineb 1 haiguses |
| RIPK4receptor interacting serine/threonine kinase 4 | Pole registreeritud | Esineb 1 haiguses |
| SMARCA2SWI/SNF related BAF chromatin remodeling complex subunit ATPase 2 | Pole registreeritud | Esineb 1 haiguses |
| UROSuroporphyrinogen III synthase | Pole registreeritud | Esineb 1 haiguses |
Kui sageli see esineb geenist tulenevate seisunditega inimeste seas, kõige sagedamini nende kõigi seas, nagu on märgitud Inimese fenotüübi ontoloogias. Need lehed kirjeldavad tunnuseid ja nende taga olevaid uuringuid; need ei ole diagnoos ning sümptomite kohta tuleks küsida arstilt või geneetilt nõustajalt.
Laiemad tunnused
Allikas
- Inimese fenotüübi ontoloogia, versioon 2026-09-01: tunnus, selle nimetused, määratlus ja sellega seotud geenid. Lisateave leiab aadressilt hpo.jax.org.
- Andmeversioon 2026.10.19-9814e911.
AtlasKellele me abiks olemeMeie teadusTootedTulemused
Logi sisseKüsiSekveneeri oma genoom↗
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.
Alates 449 $
Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
