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Træk
Increased respiratory rate or depth of breathing
Klinisk navn: Tachypnea
Very rapid breathing.
Resumé
- Også kaldet
- Polypnea
- Kropssystem
- Abnormality of the respiratory system
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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/tachypnea.json"
page <- fromJSON(url)
page$trait$nameHvem vi hjælperVores videnskabProdukterResultater
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Læs de gener, der er knyttet til Increased respiratory rate or depth of breathing, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test41 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.
- Surfactant Metabolism DysfunctionReads 5 of these genesSFTPCSFTPBABCA3CSF2RACSF2RBAbout this report →
- Joubert Syndrome And Related DisordersReads 11 of these genesCC2D2ACEP290TMEM138TMEM216TMEM231TMEM237About this report →
- Biotinidase & Holocarboxylase DeficiencyReads 2 of these genesHLCSBTDAbout this report →
- Malignant Hyperthermia SusceptibilityReads 2 of these genesCACNA1SRYR1About this report →
Show 37 more reports
- Urea Cycle DisorderReads 4 of these genesASLCA5ANAGSSLC25A15About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 8 of these genesCC2D2ACEP290TMEM138TMEM216TMEM231TMEM237About this report →
- Amyotrophic Lateral Sclerosis Susceptibility 24 (NEK1)Reads 1 of these genesNEK1About this report →
- CEP290-Related CiliopathyReads 1 of these genesCEP290About this report →
- Pulmonary Alveolar MicrolithiasisReads 1 of these genesSLC34A2About this report →
- Very Long Chain Acyl-Coa Dehydrogenase DeficiencyReads 1 of these genesACADVLAbout this report →
- X-Linked Chondrodysplasia Punctata 1Reads 1 of these genesARSLAbout this report →
- Methylmalonic & Propionic AcidemiaReads 3 of these genesABCD4PCCAPCCBAbout this report →
- Classic Organic AciduriasReads 2 of these genesACAT1HMGCLAbout this report →
- Red Blood Cell Membrane DisordersReads 2 of these genesRHAGRHCEAbout this report →
- Meckel SyndromeReads 2 of these genesTMEM231RPGRIP1LAbout this report →
- Type I InterferonopathiesReads 2 of these genesSTING1COPAAbout this report →
- Familial Periodic ParalysisReads 1 of these genesCACNA1SAbout this report →
- Fatty Acid Oxidation & Carnitine Cycle DisordersReads 2 of these genesHMGCLACADVLAbout this report →
- Moyamoya DiseaseReads 1 of these genesACTA2About this report →
- Inherited Neurodegenerative DisordersReads 9 of these genesCC2D2ACEP290TMEM138TMEM216TMEM231TMEM237About this report →
- Inherited Parathyroid & Calcium-Sensing DisordersReads 1 of these genesCASRAbout this report →
- Leigh SyndromeReads 3 of these genesSCO2BTDLRPPRCAbout this report →
- Rare Monogenic Autoinflammatory DiseasesReads 2 of these genesSTING1COPAAbout this report →
- Primary Mitochondrial DiseaseReads 4 of these genesCOA6LYRM7SCO2LRPPRCAbout this report →
- Aortic AneurysmReads 1 of these genesACTA2About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesTLL1About this report →
- Myofibrillar MyopathiesReads 1 of these genesRYR1About this report →
- Rare Hereditary Peripheral NeuropathiesReads 4 of these genesSCO2BTDIGHMBP2LRPPRCAbout this report →
- Charcot-Marie-Tooth DiseaseReads 2 of these genesSCO2IGHMBP2About this report →
- Congenital HypothyroidismReads 1 of these genesNKX2-1About this report →
- Congenital MyopathiesReads 1 of these genesRYR1About this report →
- Homocystinuria & Cobalamin DisordersReads 1 of these genesABCD4About this report →
- Nephronophthisis and Senior-Løken SyndromeReads 1 of these genesZNF423About this report →
- Leber Congenital Amaurosis & RPE65-Related RetinopathyReads 1 of these genesCEP290About this report →
- Bardet-Biedl and Alström SyndromesReads 1 of these genesCEP290About this report →
- Spinal Muscular AtrophyReads 1 of these genesIGHMBP2About this report →
- Thyroid CancerReads 1 of these genesCASRAbout this report →
- Hypogonadotropic HypogonadismReads 1 of these genesPLXND1About this report →
- Hypertrophic CardiomyopathyReads 1 of these genesACADVLAbout this report →
- Retinitis PigmentosaReads 1 of these genesCC2D2AAbout this report →
- Other Inborn Errors of ImmunityReads 1 of these genesPTCRAAbout this report →
Læs de gener, der er knyttet til Increased respiratory rate or depth of breathing, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test58 gener knyttet til Increased respiratory rate or depth of breathing
Ændringer i disse gener forårsager sjældne tilstande, hvor Increased respiratory rate or depth of breathing 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 |
|---|---|---|
| ATP5F1BATP synthase F1 subunit beta | Altid | I 1 tilstand |
| BOLA3bolA family member 3 | Altid | I 1 tilstand |
| COA6cytochrome c oxidase assembly factor 6 | Altid | I 1 tilstand |
| DMRT2doublesex and mab-3 related transcription factor 2 | Altid | I 1 tilstand |
| FARSBphenylalanyl-tRNA synthetase subunit beta | Altid | I 1 tilstand |
| GET3guided entry of tail-anchored proteins factor 3, ATPase | Altid | I 1 tilstand |
| LYRM7LYR motif containing 7 | Altid | I 1 tilstand |
| PTCRApre T cell antigen receptor alpha | Altid | I 1 tilstand |
| SCO2synthesis of cytochrome C oxidase 2 | Altid | I 1 tilstand |
| SFTPCsurfactant protein C | Altid | I 2 tilstande |
| TM2D3TM2 domain containing 3 | Altid | I 1 tilstand |
| ACAT1acetyl-CoA acetyltransferase 1 | Meget ofte (80–99 %) | I 1 tilstand |
| ACTA2actin alpha 2, smooth muscle | Meget ofte (80–99 %) | I 1 tilstand |
| CC2D2Acoiled-coil and C2 domain containing 2A | Meget ofte (80–99 %) | I 1 tilstand |
| CEP290centrosomal protein 290 | Meget ofte (80–99 %) | I 1 tilstand |
| SFTPBsurfactant protein B | Meget ofte (80–99 %) | I 3 tilstande |
| TMEM138transmembrane protein 138 | Meget ofte (80–99 %) | I 1 tilstand |
| TMEM216transmembrane protein 216 | Meget ofte (80–99 %) | I 1 tilstand |
| TMEM231transmembrane protein 231 | Meget ofte (80–99 %) | I 1 tilstand |
| TMEM237transmembrane protein 237 | Meget ofte (80–99 %) | I 1 tilstand |
| ZNF423zinc finger protein 423 | Meget ofte (80–99 %) | I 1 tilstand |
| ABCA3ATP binding cassette subfamily A member 3 | Ofte (30–79 %) | I 2 tilstande |
| ASLargininosuccinate lyase | Ofte (30–79 %) | I 1 tilstand |
| CA5Acarbonic anhydrase 5A | Ofte (30–79 %) | I 1 tilstand |
| CACNA1Scalcium voltage-gated channel subunit alpha1 S | Ofte (30–79 %) | I 1 tilstand |
| CSPP1centrosome and spindle pole associated protein 1 | Ofte (30–79 %) | I 1 tilstand |
| HLCSholocarboxylase synthetase | Ofte (30–79 %) | I 2 tilstande |
| HMGCL3-hydroxy-3-methylglutaryl-CoA lyase | Ofte (30–79 %) | I 1 tilstand |
| KIAA0586KIAA0586 | Ofte (30–79 %) | I 2 tilstande |
| NAGSN-acetylglutamate synthase | Ofte (30–79 %) | I 1 tilstand |
| NKX2-1NK2 homeobox 1 | Ofte (30–79 %) | I 1 tilstand |
| OXCT13-oxoacid CoA-transferase 1 | Ofte (30–79 %) | I 2 tilstande |
| PLXND1plexin D1 | Ofte (30–79 %) | I 1 tilstand |
| RYR1ryanodine receptor 1 | Ofte (30–79 %) | I 2 tilstande |
| SLC25A15solute carrier family 25 member 15 | Ofte (30–79 %) | I 1 tilstand |
| STING1stimulator of interferon response cGAMP interactor 1 | Ofte (30–79 %) | I 1 tilstand |
| ARMC9armadillo repeat containing 9 | Nogle gange (5–29 %) | I 1 tilstand |
| ARSLarylsulfatase L | Nogle gange (5–29 %) | I 1 tilstand |
| BTDbiotinidase | Nogle gange (5–29 %) | I 1 tilstand |
| COPAcoat protein complex I subunit alpha | Nogle gange (5–29 %) | I 1 tilstand |
Vis 18 gener mere
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| CSF2RAcolony stimulating factor 2 receptor subunit alpha | Nogle gange (5–29 %) | I 2 tilstande |
| CSF2RBcolony stimulating factor 2 receptor subunit beta | Nogle gange (5–29 %) | I 1 tilstand |
| MT-CYBmitochondrially encoded cytochrome b | Nogle gange (5–29 %) | I 1 tilstand |
| NEK1NIMA related kinase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| RHAGRh associated glycoprotein | Nogle gange (5–29 %) | I 1 tilstand |
| RHCERh blood group CcEe antigens | Nogle gange (5–29 %) | I 1 tilstand |
| RHDRh blood group D antigen | Nogle gange (5–29 %) | I 1 tilstand |
| SLC34A2solute carrier family 34 member 2 | Nogle gange (5–29 %) | I 1 tilstand |
| TLL1tolloid like 1 | Nogle gange (5–29 %) | I 1 tilstand |
| ACADVLacyl-CoA dehydrogenase very long chain | Sjældent (1–4%) | I 2 tilstande |
| ABCD4ATP binding cassette subfamily D member 4 | Ikke registreret | I 1 tilstand |
| CASRcalcium sensing receptor | Ikke registreret | I 1 tilstand |
| IGHMBP2immunoglobulin mu DNA binding protein 2 | Ikke registreret | I 1 tilstand |
| LRPPRCleucine rich pentatricopeptide repeat containing | Ikke registreret | I 1 tilstand |
| PAM16presequence translocase associated motor 16 | Ikke registreret | I 1 tilstand |
| PCCApropionyl-CoA carboxylase subunit alpha | Ikke registreret | I 1 tilstand |
| PCCBpropionyl-CoA carboxylase subunit beta | Ikke registreret | I 1 tilstand |
| RPGRIP1LRPGRIP1 like | 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
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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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