Kenmerk
Increased respiratory rate or depth of breathing
Klinische naam: Tachypnea
Very rapid breathing.
Samenvatting
- Ook bekend als
- Polypnea
- Lichaamssysteem
- Abnormality of the respiratory system
Deze pagina als gegevens
Voeg .json toe aan het adres van de pagina, of vraag application/json aan, om haar als JSON te lezen.
library(jsonlite)
url <- "https://dantelabs.com/traits/tachypnea.json"
page <- fromJSON(url)
page$trait$nameLees de genen die aan Increased respiratory rate or depth of breathing gekoppeld zijn, en de rest van uw genoom, met één test.
Vanaf $ 449Gratis verzending · Resultaten binnen 6–8 weken
Mijn Genome Test bestellen41 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 →
Lees de genen die aan Increased respiratory rate or depth of breathing gekoppeld zijn, en de rest van uw genoom, met één test.
Vanaf $ 449Gratis verzending · Resultaten binnen 6–8 weken
Mijn Genome Test bestellen58 genen gekoppeld aan Increased respiratory rate or depth of breathing
Veranderingen in deze genen veroorzaken zeldzame aandoeningen waarbij Increased respiratory rate or depth of breathing voorkomt. De meeste mensen met dit kenmerk hebben geen van die aandoeningen, en een gen op deze lijst zegt niets over het eigen genoom van iemand.
| Gen | Hoe vaak het voorkomt | Aandoeningen |
|---|---|---|
| ATP5F1BATP synthase F1 subunit beta | Altijd | In 1 aandoening |
| BOLA3bolA family member 3 | Altijd | In 1 aandoening |
| COA6cytochrome c oxidase assembly factor 6 | Altijd | In 1 aandoening |
| DMRT2doublesex and mab-3 related transcription factor 2 | Altijd | In 1 aandoening |
| FARSBphenylalanyl-tRNA synthetase subunit beta | Altijd | In 1 aandoening |
| GET3guided entry of tail-anchored proteins factor 3, ATPase | Altijd | In 1 aandoening |
| LYRM7LYR motif containing 7 | Altijd | In 1 aandoening |
| PTCRApre T cell antigen receptor alpha | Altijd | In 1 aandoening |
| SCO2synthesis of cytochrome C oxidase 2 | Altijd | In 1 aandoening |
| SFTPCsurfactant protein C | Altijd | In 2 aandoeningen |
| TM2D3TM2 domain containing 3 | Altijd | In 1 aandoening |
| ACAT1acetyl-CoA acetyltransferase 1 | Heel vaak (80–99%) | In 1 aandoening |
| ACTA2actin alpha 2, smooth muscle | Heel vaak (80–99%) | In 1 aandoening |
| CC2D2Acoiled-coil and C2 domain containing 2A | Heel vaak (80–99%) | In 1 aandoening |
| CEP290centrosomal protein 290 | Heel vaak (80–99%) | In 1 aandoening |
| SFTPBsurfactant protein B | Heel vaak (80–99%) | In 3 aandoeningen |
| TMEM138transmembrane protein 138 | Heel vaak (80–99%) | In 1 aandoening |
| TMEM216transmembrane protein 216 | Heel vaak (80–99%) | In 1 aandoening |
| TMEM231transmembrane protein 231 | Heel vaak (80–99%) | In 1 aandoening |
| TMEM237transmembrane protein 237 | Heel vaak (80–99%) | In 1 aandoening |
| ZNF423zinc finger protein 423 | Heel vaak (80–99%) | In 1 aandoening |
| ABCA3ATP binding cassette subfamily A member 3 | Vaak (30–79%) | In 2 aandoeningen |
| ASLargininosuccinate lyase | Vaak (30–79%) | In 1 aandoening |
| CA5Acarbonic anhydrase 5A | Vaak (30–79%) | In 1 aandoening |
| CACNA1Scalcium voltage-gated channel subunit alpha1 S | Vaak (30–79%) | In 1 aandoening |
| CSPP1centrosome and spindle pole associated protein 1 | Vaak (30–79%) | In 1 aandoening |
| HLCSholocarboxylase synthetase | Vaak (30–79%) | In 2 aandoeningen |
| HMGCL3-hydroxy-3-methylglutaryl-CoA lyase | Vaak (30–79%) | In 1 aandoening |
| KIAA0586KIAA0586 | Vaak (30–79%) | In 2 aandoeningen |
| NAGSN-acetylglutamate synthase | Vaak (30–79%) | In 1 aandoening |
| NKX2-1NK2 homeobox 1 | Vaak (30–79%) | In 1 aandoening |
| OXCT13-oxoacid CoA-transferase 1 | Vaak (30–79%) | In 2 aandoeningen |
| PLXND1plexin D1 | Vaak (30–79%) | In 1 aandoening |
| RYR1ryanodine receptor 1 | Vaak (30–79%) | In 2 aandoeningen |
| SLC25A15solute carrier family 25 member 15 | Vaak (30–79%) | In 1 aandoening |
| STING1stimulator of interferon response cGAMP interactor 1 | Vaak (30–79%) | In 1 aandoening |
| ARMC9armadillo repeat containing 9 | Soms (5–29%) | In 1 aandoening |
| ARSLarylsulfatase L | Soms (5–29%) | In 1 aandoening |
| BTDbiotinidase | Soms (5–29%) | In 1 aandoening |
| COPAcoat protein complex I subunit alpha | Soms (5–29%) | In 1 aandoening |
Toon nog 18 genen
| Gen | Hoe vaak het voorkomt | Aandoeningen |
|---|---|---|
| CSF2RAcolony stimulating factor 2 receptor subunit alpha | Soms (5–29%) | In 2 aandoeningen |
| CSF2RBcolony stimulating factor 2 receptor subunit beta | Soms (5–29%) | In 1 aandoening |
| MT-CYBmitochondrially encoded cytochrome b | Soms (5–29%) | In 1 aandoening |
| NEK1NIMA related kinase 1 | Soms (5–29%) | In 1 aandoening |
| RHAGRh associated glycoprotein | Soms (5–29%) | In 1 aandoening |
| RHCERh blood group CcEe antigens | Soms (5–29%) | In 1 aandoening |
| RHDRh blood group D antigen | Soms (5–29%) | In 1 aandoening |
| SLC34A2solute carrier family 34 member 2 | Soms (5–29%) | In 1 aandoening |
| TLL1tolloid like 1 | Soms (5–29%) | In 1 aandoening |
| ACADVLacyl-CoA dehydrogenase very long chain | Zelden (1–4%) | In 2 aandoeningen |
| ABCD4ATP binding cassette subfamily D member 4 | Niet vastgelegd | In 1 aandoening |
| CASRcalcium sensing receptor | Niet vastgelegd | In 1 aandoening |
| IGHMBP2immunoglobulin mu DNA binding protein 2 | Niet vastgelegd | In 1 aandoening |
| LRPPRCleucine rich pentatricopeptide repeat containing | Niet vastgelegd | In 1 aandoening |
| PAM16presequence translocase associated motor 16 | Niet vastgelegd | In 1 aandoening |
| PCCApropionyl-CoA carboxylase subunit alpha | Niet vastgelegd | In 1 aandoening |
| PCCBpropionyl-CoA carboxylase subunit beta | Niet vastgelegd | In 1 aandoening |
| RPGRIP1LRPGRIP1 like | Niet vastgelegd | In 1 aandoening |
Hoe vaak dit voorkomt bij mensen met een van de aandoeningen van het gen, de hoogste frequentie binnen die aandoeningen, zoals de Human Phenotype Ontology dit vastlegt. Deze pagina's beschrijven kenmerken en het onderzoek erachter; het zijn geen diagnose, en over symptomen kunt u het best een arts of genetisch adviseur raadplegen.
Smallere kenmerken
Bredere kenmerken
Waar dit vandaan komt
- De Human Phenotype Ontology, release 2026-09-01: het kenmerk, de namen, de definitie en de genen die ermee verbonden zijn. Meer informatie vindt u op hpo.jax.org.
- Gegevensrelease 2026.10.19-9814e911.
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.
Gratis verzending · Resultaten binnen 6–8 weken
