AtlasKellele me abiks olemeMeie teadusTootedTulemused
Logi sisseKüsiSekveneeri oma genoom↗
Tunnus
Obstructive sleep apnea
Obstructive Sleep Apnea is a condition characterized by the obstruction of the airway and pauses in breathing during sleep, which occur multiple times throughout the night. It is related to the relaxation of muscle tone that typically happens during sleep, leading to a partial collapse of the soft tissues in the airway and causing airflow obstruction.
Kokkuvõte
- Kehasüsteem
- Abnormality of the nervous system
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/obstructive-sleep-apnea.json"
page <- fromJSON(url)
page$trait$nameObstructive sleep apneaHP:0002870
AtlasKellele me abiks olemeMeie teadusTootedTulemused
Logi sisseKüsiSekveneeri oma genoom↗
Lugege välja geenid, mis on seotud Obstructive sleep apnea-ga, ja kogu ülejäänud genoom ühe testiga.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test59 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.
- Auriculocondylar Syndrome 2 (PLCB4)Reads 1 of these genesPLCB4About this report →
- CherubismReads 1 of these genesSH3BP2About this report →
- Dystrophinopathies (Duchenne and Becker Muscular Dystrophy)Reads 1 of these genesDMDAbout this report →
- Ferguson-Smith Disease (Multiple Self-Healing Squamous Epithelioma)Reads 1 of these genesTGFBR1About this report →
Show 55 more reports
- FGFR3-Related Chondrodysplasias (Achondroplasia and Related Conditions)Reads 1 of these genesFGFR3About this report →
- Marshall-Smith SyndromeReads 1 of these genesNFIXAbout this report →
- MCM3AP-Related Peripheral NeuropathyReads 1 of these genesMCM3APAbout this report →
- Mucopolysaccharidosis Type I (Hurler and Scheie Syndromes)Reads 1 of these genesIDUAAbout this report →
- Mucopolysaccharidosis Type II (Hunter Syndrome)Reads 1 of these genesIDSAbout this report →
- Mucopolysaccharidosis Type VII (Sly Syndrome)Reads 1 of these genesGUSBAbout this report →
- NGLY1 DeficiencyReads 1 of these genesNGLY1About this report →
- Primary Failure of Tooth EruptionReads 1 of these genesPTH1RAbout this report →
- TRPV4-Related Skeletal DysplasiasReads 1 of these genesTRPV4About this report →
- Turnpenny-Fry SyndromeReads 1 of these genesPCGF2About this report →
- Marfan Like SyndromesReads 3 of these genesTGFBR1FBN1SKIAbout this report →
- Syndromic CraniosynostosisReads 4 of these genesFGFR3RECQL4SKIZNF462About this report →
- Intellectual DisabilityReads 12 of these genesAHDC1ASXL1CHAMP1CREBBPEP300POGZAbout this report →
- Cerebral Arteriopathy with Subcortical Infarcts and LeukoencephalopathyReads 1 of these genesNOTCH3About this report →
- Myotonic DystrophyReads 1 of these genesCNBPAbout this report →
- PRR12-Related Neuroocular SyndromeReads 1 of these genesPRR12About this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 2 of these genesMAGEL2SNRPNAbout this report →
- Lysosomal Storage DiseaseReads 5 of these genesCTSKGNPTABGUSBIDSIDUAAbout this report →
- Mucolipidoses (ML II, ML III and ML IV)Reads 1 of these genesGNPTABAbout this report →
- Rothmund-Thomson SyndromeReads 1 of these genesRECQL4About this report →
- Van der Woude and Popliteal Pterygium Syndromes (IRF6)Reads 1 of these genesGRHL3About this report →
- Aortic AneurysmReads 2 of these genesTGFBR1FBN1About this report →
- OsteopetrosisReads 2 of these genesCTSKCA2About this report →
- Overgrowth Syndromes (Sotos, Weaver, Tatton-Brown-Rahman, Malan)Reads 1 of these genesNFIXAbout this report →
- Periventricular Nodular HeterotopiaReads 1 of these genesFLNAAbout this report →
- Syndromic Complex Neurodevelopmental DisorderReads 2 of these genesZFXZMYM2About this report →
- Hereditary Orofacial CleftingReads 1 of these genesGRHL3About this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 1 of these genesFLNAAbout this report →
- Heritable Pulmonary Arterial Hypertension (HPAH)Reads 1 of these genesKCNK3About this report →
- Loeys-Dietz SyndromeReads 1 of these genesTGFBR1About this report →
- Inherited Predisposition to Acute Myeloid LeukaemiaReads 1 of these genesTERTAbout this report →
- Monogenic Obesity (Leptin-Melanocortin Pathway)Reads 1 of these genesSIM1About this report →
- Epilepsy (Full Panel)Reads 5 of these genesFBXO28FLNARNU2-2GRIN1NACC1About this report →
- Oculocutaneous AlbinismReads 1 of these genesOCA2About this report →
- Familial Pulmonary FibrosisReads 1 of these genesTERTAbout this report →
- Long QT SyndromeReads 1 of these genesCACNA1CAbout this report →
- Congenital Anomalies of the Kidney and Urinary TractReads 1 of these genesSOX17About this report →
- Hypogonadotropic HypogonadismReads 2 of these genesMAGEL2SNRPNAbout this report →
- Inherited Congenital Heart DefectsReads 1 of these genesFLNAAbout this report →
- Hypertrophic CardiomyopathyReads 2 of these genesALPK3HRASAbout this report →
- Congenital MyopathiesReads 1 of these genesTNNT1About this report →
- GPI Anchor Biosynthesis DefectsReads 1 of these genesPIGTAbout this report →
- Noonan SyndromeReads 1 of these genesHRASAbout this report →
- Dyskeratosis CongenitaReads 1 of these genesTERTAbout this report →
- Congenital Disorders of GlycosylationReads 2 of these genesDHRSXPIGTAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 3 of these genesBICD2LRPPRCTRPV4About this report →
- Spinal Muscular AtrophyReads 1 of these genesBICD2About this report →
- Primary Mitochondrial DiseaseReads 2 of these genesDNA2LRPPRCAbout this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 1 of these genesATN1About this report →
- Inherited Neurodegenerative DisordersReads 3 of these genesFLVCR1ATN1BICD2About this report →
- Dilated CardiomyopathyReads 1 of these genesDMDAbout this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesFLVCR1About this report →
- Leigh SyndromeReads 1 of these genesLRPPRCAbout this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesTRPV4About this report →
- Retinitis PigmentosaReads 1 of these genesFLVCR1About this report →
Lugege välja geenid, mis on seotud Obstructive sleep apnea-ga, ja kogu ülejäänud genoom ühe testiga.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test92 geeni on seotud tunnusega Obstructive sleep apnea
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Obstructive sleep apnea. 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 |
|---|---|---|
| ALPK3alpha kinase 3 | Alati | Esineb 1 haiguses |
| AMOTL1angiomotin like 1 | Alati | Esineb 1 haiguses |
| ATXN7L3ataxin 7 like 3 | Alati | Esineb 1 haiguses |
| CACNA1Ccalcium voltage-gated channel subunit alpha1 C | Alati | Esineb 1 haiguses |
| DMDdystrophin | Alati | Esineb 1 haiguses |
| DOT1LDOT1 like histone lysine methyltransferase | Alati | Esineb 1 haiguses |
| FBXO28F-box protein 28 | Alati | Esineb 1 haiguses |
| FLNAfilamin A | Alati | Esineb 1 haiguses |
| FLVCR1FLVCR choline and heme transporter 1 | Alati | Esineb 1 haiguses |
| FXR1FMR1 autosomal homolog 1 | Alati | Esineb 2 haiguses |
| MED16mediator complex subunit 16 | Alati | Esineb 1 haiguses |
| MSL2MSL complex subunit 2 | Alati | Esineb 1 haiguses |
| RFC4replication factor C subunit 4 | Alati | Esineb 1 haiguses |
| RNU2-2RNA, U2 small nuclear 2 | Alati | Esineb 1 haiguses |
| SOX17SRY-box transcription factor 17 | Alati | Esineb 1 haiguses |
| WSB2WD repeat and SOCS box containing 2 | Alati | Esineb 1 haiguses |
| AHDC1AT-hook DNA binding motif containing 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| ADRA2Aadrenoceptor alpha 2A | Sageli (30–79%) | Esineb 1 haiguses |
| ASXL1ASXL transcriptional regulator 1 | Sageli (30–79%) | Esineb 1 haiguses |
| ATN1atrophin 1 | Sageli (30–79%) | Esineb 1 haiguses |
| BMP2bone morphogenetic protein 2 | Sageli (30–79%) | Esineb 1 haiguses |
| CACNA2D1calcium voltage-gated channel auxiliary subunit alpha2delta 1 | Sageli (30–79%) | Esineb 1 haiguses |
| CCDC47coiled-coil domain containing 47 | Sageli (30–79%) | Esineb 1 haiguses |
| CHAMP1chromosome alignment maintaining phosphoprotein 1 | Sageli (30–79%) | Esineb 1 haiguses |
| CREBBPCREB binding lysine acetyltransferase | Sageli (30–79%) | Esineb 3 haiguses |
| CTSKcathepsin K | Sageli (30–79%) | Esineb 1 haiguses |
| DNA2DNA replication helicase/nuclease 2 | Sageli (30–79%) | Esineb 2 haiguses |
| DVL1dishevelled segment polarity protein 1 | Sageli (30–79%) | Esineb 1 haiguses |
| EDN1endothelin 1 | Sageli (30–79%) | Esineb 1 haiguses |
| EP300EP300 lysine acetyltransferase | Sageli (30–79%) | Esineb 2 haiguses |
| EXOC2exocyst complex component 2 | Sageli (30–79%) | Esineb 1 haiguses |
| FGFR3fibroblast growth factor receptor 3 | Sageli (30–79%) | Esineb 1 haiguses |
| GNAI3G protein subunit alpha i3 | Sageli (30–79%) | Esineb 1 haiguses |
| GNPTABN-acetylglucosamine-1-phosphate transferase subunits alpha and beta | Sageli (30–79%) | Esineb 1 haiguses |
| GRHL3grainyhead like transcription factor 3 | Sageli (30–79%) | Esineb 1 haiguses |
| GUSBglucuronidase beta | Sageli (30–79%) | Esineb 1 haiguses |
| KCNK3potassium two pore domain channel subfamily K member 3 | Sageli (30–79%) | Esineb 1 haiguses |
| MOGmyelin oligodendrocyte glycoprotein | Sageli (30–79%) | Esineb 1 haiguses |
| NFIXnuclear factor I X | Sageli (30–79%) | Esineb 1 haiguses |
| NGLY1N-glycanase 1 | Sageli (30–79%) | Esineb 1 haiguses |
Näita veel 52 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| NOTCH3notch receptor 3 | Sageli (30–79%) | Esineb 1 haiguses |
| PLCB4phospholipase C beta 4 | Sageli (30–79%) | Esineb 1 haiguses |
| POGZpogo transposable element derived with ZNF domain | Sageli (30–79%) | Esineb 2 haiguses |
| PRKAR1Bprotein kinase cAMP-dependent type I regulatory subunit beta | Sageli (30–79%) | Esineb 1 haiguses |
| PRR12proline rich 12 | Sageli (30–79%) | Esineb 1 haiguses |
| PTH1Rparathyroid hormone 1 receptor | Sageli (30–79%) | Esineb 1 haiguses |
| RNH1ribonuclease/angiogenin inhibitor 1 | Sageli (30–79%) | Esineb 1 haiguses |
| TGFBR1transforming growth factor beta receptor 1 | Sageli (30–79%) | Esineb 1 haiguses |
| UBBubiquitin B | Sageli (30–79%) | Esineb 1 haiguses |
| ADAMTSL2ADAMTS like 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ARCN1archain 1 coat protein complex I subunit delta | Mõnikord (5–29%) | Esineb 1 haiguses |
| BICD2BICD cargo adaptor 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CAPRIN1cell cycle associated protein 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CDC42BPBCDC42 binding protein kinase beta | Mõnikord (5–29%) | Esineb 1 haiguses |
| CNBPCCHC-type zinc finger nucleic acid binding protein | Mõnikord (5–29%) | Esineb 1 haiguses |
| CRELD1CRELD disulfide isomerase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DDB1damage specific DNA binding protein 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DHRSXdehydrogenase/reductase X-linked | Mõnikord (5–29%) | Esineb 1 haiguses |
| DPH5diphthamide biosynthesis 5 | Mõnikord (5–29%) | Esineb 1 haiguses |
| FBN1fibrillin 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GRB10growth factor receptor bound protein 10 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GRIN1glutamate ionotropic receptor NMDA type subunit 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| H4C5H4 clustered histone 5 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HNRNPCheterogeneous nuclear ribonucleoprotein C | Mõnikord (5–29%) | Esineb 1 haiguses |
| LRPPRCleucine rich pentatricopeptide repeat containing | Mõnikord (5–29%) | Esineb 1 haiguses |
| LTBP3latent transforming growth factor beta binding protein 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MAGEL2MAGE family member L2 | Mõnikord (5–29%) | Esineb 4 haiguses |
| MCM3APminichromosome maintenance complex component 3 associated protein | Mõnikord (5–29%) | Esineb 1 haiguses |
| NACC1nucleus accumbens associated 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NDNnecdin, MAGE family member | Mõnikord (5–29%) | Esineb 3 haiguses |
| NONOnon-POU domain containing octamer binding | Mõnikord (5–29%) | Esineb 1 haiguses |
| OCA2OCA2 melanosomal transmembrane protein | Mõnikord (5–29%) | Esineb 3 haiguses |
| PIGTphosphatidylinositol glycan anchor biosynthesis class T | Mõnikord (5–29%) | Esineb 1 haiguses |
| RAB11BRAB11B, member RAS oncogene family | Mõnikord (5–29%) | Esineb 1 haiguses |
| RECQL4RecQ like helicase 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SATB2SATB homeobox 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SH3BP2SH3 domain binding protein 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SIM1SIM bHLH transcription factor 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SKISKI proto-oncogene | Mõnikord (5–29%) | Esineb 1 haiguses |
| SNRPNsmall nuclear ribonucleoprotein polypeptide N | Mõnikord (5–29%) | Esineb 3 haiguses |
| TERTtelomerase reverse transcriptase | Mõnikord (5–29%) | Esineb 1 haiguses |
| TNNT1troponin T1, slow skeletal type | Mõnikord (5–29%) | Esineb 1 haiguses |
| ZFXzinc finger protein X-linked | Mõnikord (5–29%) | Esineb 1 haiguses |
| ZMYM2zinc finger MYM-type containing 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ZNF462zinc finger protein 462 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ACBD6acyl-CoA binding domain containing 6 | Harva (1–4%) | Esineb 1 haiguses |
| CA2carbonic anhydrase 2 | Harva (1–4%) | Esineb 1 haiguses |
| HRASHRas proto-oncogene, GTPase | Pole registreeritud | Esineb 1 haiguses |
| IDSiduronate 2-sulfatase | Pole registreeritud | Esineb 1 haiguses |
| IDUAalpha-L-iduronidase | Pole registreeritud | Esineb 2 haiguses |
| PCGF2polycomb group ring finger 2 | Pole registreeritud | Esineb 1 haiguses |
| TRPV4transient receptor potential cation channel subfamily V member 4 | 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
