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Egenskap
Pauses in breathing while sleeping
Kliniskt namn: Sleep apnea
An intermittent cessation of airflow at the mouth and nose during sleep is known as sleep apnea. Apneas that last at least 10 seconds are considered significant, but individuals with sleep apnea may experience apneas lasting from 20 seconds up to 2 or 3 minutes. Patients may have up to 15 events per hour of sleep.
Sammanfattning
- Även kallad
- Sleep apnoea
- Kroppssystem
- Abnormality of the nervous system
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library(jsonlite)
url <- "https://dantelabs.com/traits/sleep-apnea.json"
page <- fromJSON(url)
page$trait$namePauses in breathing while sleepingHP:0010535
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Läs generna kopplade till Pauses in breathing while sleeping, och resten av ditt genom, med ett enda test.
Från 449 $Fri frakt · Resultat inom 6–8 veckor
Beställ mitt Genome Test61 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.
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- Asparagine Synthetase DeficiencyReads 1 of these genesASNSAbout this report →
- ATP1A2-Related Fetal Akinesia with PolymicrogyriaReads 1 of these genesATP1A2About this report →
- Bent Bone Dysplasia Syndrome (FGFR2)Reads 1 of these genesFGFR2About this report →
Show 57 more reports
- Birt-Hogg-Dubé SyndromeReads 1 of these genesFLCNAbout this report →
- Campomelic DysplasiaReads 1 of these genesSOX9About this report →
- CTNNB1 SyndromeReads 1 of these genesCTNNB1About this report →
- DPH1-Related Developmental Delay with Short StatureReads 1 of these genesDPH1About this report →
- FGFR3-Related Chondrodysplasias (Achondroplasia and Related Conditions)Reads 1 of these genesFGFR3About this report →
- Friedreich AtaxiaReads 1 of these genesFXNAbout this report →
- Genetic Prion Disease (incl. Fatal Familial Insomnia)Reads 1 of these genesPRNPAbout this report →
- Hao-Fountain SyndromeReads 1 of these genesUSP7About this report →
- MED27-Related Neurodevelopmental DisorderReads 1 of these genesMED27About this report →
- Mucopolysaccharidosis Type II (Hunter Syndrome)Reads 1 of these genesIDSAbout this report →
- Mucopolysaccharidosis Type VI (Maroteaux-Lamy Syndrome)Reads 1 of these genesARSBAbout this report →
- Orofaciodigital Syndrome Type 14Reads 1 of these genesC2CD3About this report →
- SPOP-Related Neurodevelopmental Disorder with MacrocephalyReads 1 of these genesSPOPAbout this report →
- Cantú SyndromeReads 1 of these genesABCC9About this report →
- Cleidocranial DysplasiaReads 1 of these genesRUNX2About this report →
- Encephalopathy due to Mitochondrial and Peroxisomal Fission DefectReads 1 of these genesDNM1LAbout this report →
- Hereditary Multiple OsteochondromasReads 1 of these genesEXT2About this report →
- Syndromic CraniosynostosisReads 3 of these genesFGFR2FGFR3TWIST1About this report →
- Congenital Myasthenic SyndromeReads 3 of these genesMUSKCOL13A1COLQAbout this report →
- Familial Hemiplegic MigraineReads 1 of these genesATP1A2About this report →
- Monogenic Precocious PubertyReads 1 of these genesMKRN3About this report →
- Intellectual DisabilityReads 8 of these genesRAI1AHDC1TCF4CTNNB1PRMT7RPS6KA3About this report →
- Carney Complex & Hereditary Adrenal Cushing SyndromeReads 1 of these genesPRKAR1AAbout this report →
- Complex Neurodevelopmental Disorder (TRRAP, MYH10, RERE, SOX11)Reads 1 of these genesREREAbout this report →
- Pseudohypoparathyroidism & GNAS-Inactivation DisordersReads 1 of these genesPRKAR1AAbout this report →
- Hereditary Corneal DystrophiesReads 2 of these genesTCF4GSNAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 7 of these genesHSPB8NDUFAF2MRPS34GSNNDUFS2DCTN1About this report →
- Mosaic Variegated Aneuploidy SyndromeReads 1 of these genesCEP57About this report →
- MTOR Pathway Megalencephaly and Overgrowth DisordersReads 1 of these genesPIK3CAAbout this report →
- Lysosomal Storage DiseaseReads 3 of these genesARSBGNEIDSAbout this report →
- Spinal Muscular AtrophyReads 2 of these genesHSPB8DCTN1About this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 2 of these genesDCTN1SOD1About this report →
- Leigh SyndromeReads 3 of these genesNDUFAF2MRPS34NDUFS2About this report →
- Charcot-Marie-Tooth DiseaseReads 3 of these genesHSPB8DCTN1NEFHAbout this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 1 of these genesMAGEL2About this report →
- Kidney CancerReads 1 of these genesFLCNAbout this report →
- Inherited Neurodegenerative DisordersReads 6 of these genesDNM1LHSPB8PRNPFXNDCTN1SOD1About this report →
- Epilepsy (Full Panel)Reads 4 of these genesGABRG2GRIN2AATP1A2SLC32A1About this report →
- Hereditary AmyloidosisReads 1 of these genesGSNAbout this report →
- Urinary and Renal System TumourReads 1 of these genesFLCNAbout this report →
- Hereditary Optic NeuropathyReads 1 of these genesDNM1LAbout this report →
- Myofibrillar MyopathiesReads 1 of these genesHSPB8About this report →
- Primary Mitochondrial DiseaseReads 3 of these genesNDUFAF2MRPS34NDUFS2About this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 1 of these genesTSPYL1About this report →
- Distal MyopathiesReads 1 of these genesGNEAbout this report →
- Noonan SyndromeReads 1 of these genesBRAFAbout this report →
- Syndromic Complex Neurodevelopmental DisorderReads 1 of these genesMYT1LAbout this report →
- Congenital Disorders of GlycosylationReads 2 of these genesGNEEXT2About this report →
- VitreoretinopathyReads 1 of these genesCTNNB1About this report →
- Nephrotic SyndromeReads 1 of these genesLAMB2About this report →
- Inherited ThrombocytopeniasReads 1 of these genesGNEAbout this report →
- Joubert Syndrome And Related DisordersReads 1 of these genesARL3About this report →
- Dilated CardiomyopathyReads 1 of these genesABCC9About this report →
- Hypogonadotropic HypogonadismReads 1 of these genesMAGEL2About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesFXNAbout this report →
- Hypertrophic CardiomyopathyReads 1 of these genesBRAFAbout this report →
- Retinitis PigmentosaReads 1 of these genesARL3About this report →
Läs generna kopplade till Pauses in breathing while sleeping, och resten av ditt genom, med ett enda test.
Från 449 $Fri frakt · Resultat inom 6–8 veckor
Beställ mitt Genome Test89 gener kopplade till Pauses in breathing while sleeping
Förändringar i dessa gener orsakar sällsynta tillstånd där Pauses in breathing while sleeping förekommer. De flesta med denna egenskap har inget av dessa tillstånd, och en gen på listan säger ingenting om någons eget genom.
| Gen | Hur ofta den förekommer | Tillstånd |
|---|---|---|
| ABCC9ATP binding cassette subfamily C member 9 | Alltid | I 1 tillstånd |
| ASNSasparagine synthetase (glutamine-hydrolyzing) | Alltid | I 1 tillstånd |
| DHRS3dehydrogenase/reductase 3 | Alltid | I 1 tillstånd |
| DNM1Ldynamin 1L | Alltid | I 1 tillstånd |
| HSPB8heat shock protein family B (small) member 8 | Alltid | I 1 tillstånd |
| LRRC32leucine rich repeat containing 32 | Alltid | I 1 tillstånd |
| LRRC7leucine rich repeat containing 7 | Alltid | I 1 tillstånd |
| MUSKmuscle associated receptor tyrosine kinase | Alltid | I 1 tillstånd |
| NAA80N-alpha-acetyltransferase 80, NatH catalytic subunit | Alltid | I 1 tillstånd |
| NDUFAF2NADH:ubiquinone oxidoreductase complex assembly factor 2 | Alltid | I 1 tillstånd |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Alltid | I 1 tillstånd |
| RNU5B-1RNA, U5B small nuclear 1 | Alltid | I 1 tillstånd |
| TM2D3TM2 domain containing 3 | Alltid | I 1 tillstånd |
| UBAP2Lubiquitin associated protein 2 like | Alltid | I 1 tillstånd |
| VPS51VPS51 subunit of GARP complex | Alltid | I 1 tillstånd |
| ARSBarylsulfatase B | Mycket ofta (80–99 %) | I 1 tillstånd |
| GNEglucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase | Mycket ofta (80–99 %) | I 2 tillstånd |
| RAI1retinoic acid induced 1 | Mycket ofta (80–99 %) | I 3 tillstånd |
| TSPYL1TSPY like 1 | Mycket ofta (80–99 %) | I 1 tillstånd |
| ZBTB7Azinc finger and BTB domain containing 7A | Mycket ofta (80–99 %) | I 1 tillstånd |
| AFF4ALF transcription elongation factor 4 | Ofta (30–79 %) | I 2 tillstånd |
| AHDC1AT-hook DNA binding motif containing 1 | Ofta (30–79 %) | I 1 tillstånd |
| AIPAHR interacting HSP90 co-chaperone | Ofta (30–79 %) | I 1 tillstånd |
| C2CD3C2 domain containing 3 centriole elongation regulator | Ofta (30–79 %) | I 1 tillstånd |
| CEP57centrosomal protein 57 | Ofta (30–79 %) | I 1 tillstånd |
| GABRG2gamma-aminobutyric acid type A receptor subunit gamma2 | Ofta (30–79 %) | I 1 tillstånd |
| GPR101G protein-coupled receptor 101 | Ofta (30–79 %) | I 2 tillstånd |
| GRIN2Aglutamate ionotropic receptor NMDA type subunit 2A | Ofta (30–79 %) | I 1 tillstånd |
| HERC2HECT and RLD domain containing E3 ubiquitin protein ligase 2 | Ofta (30–79 %) | I 1 tillstånd |
| MAGEL2MAGE family member L2 | Ofta (30–79 %) | I 3 tillstånd |
| MARK2microtubule affinity regulating kinase 2 | Ofta (30–79 %) | I 1 tillstånd |
| MKRN3makorin ring finger protein 3 | Ofta (30–79 %) | I 1 tillstånd |
| MRPS34mitochondrial ribosomal protein S34 | Ofta (30–79 %) | I 1 tillstånd |
| NCAPG2non-SMC condensin II complex subunit G2 | Ofta (30–79 %) | I 1 tillstånd |
| NPAP1nuclear pore associated protein 1 | Ofta (30–79 %) | I 1 tillstånd |
| NUP54nucleoporin 54 | Ofta (30–79 %) | I 1 tillstånd |
| PRNPprion protein (Kanno blood group) | Ofta (30–79 %) | I 1 tillstånd |
| PWAR1Prader Willi/Angelman region RNA 1 | Ofta (30–79 %) | I 1 tillstånd |
| PWRN1Prader-Willi region non-protein coding RNA 1 | Ofta (30–79 %) | I 1 tillstånd |
| SNORD115-1small nucleolar RNA, C/D box 115-1 | Ofta (30–79 %) | I 1 tillstånd |
Visa 49 gener till
| Gen | Hur ofta den förekommer | Tillstånd |
|---|---|---|
| SNORD116-1small nucleolar RNA, C/D box 116-1 | Ofta (30–79 %) | I 1 tillstånd |
| SPOPspeckle type BTB/POZ protein | Ofta (30–79 %) | I 1 tillstånd |
| SRPX2sushi repeat containing protein X-linked 2 | Ofta (30–79 %) | I 1 tillstånd |
| TCF4transcription factor 4 | Ofta (30–79 %) | I 1 tillstånd |
| ARL3ARF like GTPase 3 | Ibland (5–29 %) | I 1 tillstånd |
| ATP1A2ATPase Na+/K+ transporting subunit alpha 2 | Ibland (5–29 %) | I 1 tillstånd |
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Ibland (5–29 %) | I 1 tillstånd |
| COL13A1collagen type XIII alpha 1 chain | Ibland (5–29 %) | I 1 tillstånd |
| COLQcollagen like tail subunit of asymmetric acetylcholinesterase | Ibland (5–29 %) | I 1 tillstånd |
| CTNNB1catenin beta 1 | Ibland (5–29 %) | I 1 tillstånd |
| CTSHcathepsin H | Ibland (5–29 %) | I 1 tillstånd |
| DPH1diphthamide biosynthesis 1 | Ibland (5–29 %) | I 1 tillstånd |
| DPH2diphthamide biosynthesis 2 | Ibland (5–29 %) | I 1 tillstånd |
| EXT2exostosin glycosyltransferase 2 | Ibland (5–29 %) | I 1 tillstånd |
| FGFR2fibroblast growth factor receptor 2 | Ibland (5–29 %) | I 2 tillstånd |
| FGFR3fibroblast growth factor receptor 3 | Ibland (5–29 %) | I 2 tillstånd |
| FXNfrataxin | Ibland (5–29 %) | I 1 tillstånd |
| GSNgelsolin | Ibland (5–29 %) | I 1 tillstånd |
| HCRThypocretin neuropeptide precursor | Ibland (5–29 %) | I 1 tillstånd |
| HLA-DQB1major histocompatibility complex, class II, DQ beta 1 | Ibland (5–29 %) | I 1 tillstånd |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Ibland (5–29 %) | I 1 tillstånd |
| IDSiduronate 2-sulfatase | Ibland (5–29 %) | I 1 tillstånd |
| LAMB2laminin subunit beta 2 | Ibland (5–29 %) | I 1 tillstånd |
| LARP7La ribonucleoprotein 7, transcriptional regulator | Ibland (5–29 %) | I 1 tillstånd |
| MED27mediator complex subunit 27 | Ibland (5–29 %) | I 1 tillstånd |
| MOGmyelin oligodendrocyte glycoprotein | Ibland (5–29 %) | I 1 tillstånd |
| NDUFS2NADH:ubiquinone oxidoreductase core subunit S2 | Ibland (5–29 %) | I 1 tillstånd |
| P2RY11purinergic receptor P2Y11 | Ibland (5–29 %) | I 1 tillstånd |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Ibland (5–29 %) | I 1 tillstånd |
| PRMT7protein arginine methyltransferase 7 | Ibland (5–29 %) | I 1 tillstånd |
| REREarginine-glutamic acid dipeptide repeats | Ibland (5–29 %) | I 1 tillstånd |
| RPS6KA3ribosomal protein S6 kinase A3 | Ibland (5–29 %) | I 1 tillstånd |
| RUNX2RUNX family transcription factor 2 | Ibland (5–29 %) | I 1 tillstånd |
| SIN3ASIN3 transcription regulator family member A | Ibland (5–29 %) | I 1 tillstånd |
| SLC32A1solute carrier family 32 member 1 | Ibland (5–29 %) | I 1 tillstånd |
| SOX9SRY-box transcription factor 9 | Ibland (5–29 %) | I 1 tillstånd |
| SYT1synaptotagmin 1 | Ibland (5–29 %) | I 2 tillstånd |
| TNFSF4TNF superfamily member 4 | Ibland (5–29 %) | I 1 tillstånd |
| TWIST1twist family bHLH transcription factor 1 | Ibland (5–29 %) | I 1 tillstånd |
| USP7ubiquitin specific peptidase 7 | Ibland (5–29 %) | I 1 tillstånd |
| ZNF365zinc finger protein 365 | Ibland (5–29 %) | I 1 tillstånd |
| MYT1Lmyelin transcription factor 1 like | Sällan (1–4%) | I 1 tillstånd |
| PABPN1poly(A) binding protein nuclear 1 | Sällan (1–4%) | I 1 tillstånd |
| DCTN1dynactin subunit 1 | Inte registrerat | I 1 tillstånd |
| FLCNfolliculin | Inte registrerat | I 1 tillstånd |
| LTBP3latent transforming growth factor beta binding protein 3 | Inte registrerat | I 1 tillstånd |
| NEFHneurofilament heavy chain | Inte registrerat | I 1 tillstånd |
| PRPHperipherin | Inte registrerat | I 1 tillstånd |
| SOD1superoxide dismutase 1 | Inte registrerat | I 1 tillstånd |
Hur ofta det förekommer hos personer med ett av genens tillstånd, den vanligaste frekvensen bland dem, enligt Human Phenotype Ontology. Dessa sidor beskriver egenskaper och forskningen bakom dem. De är inte en diagnos, och det är läkare eller genetisk rådgivare du bör fråga om symtom.
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Varifrån informationen kommer
- Human Phenotype Ontology, version 2026-09-01: egenskapen, dess namn, definition och de gener som är kopplade till den. Läs mer på hpo.jax.org.
- Dataversion 2026.10.21-777c9289.
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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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