Træk
Partial or complete collapse of part or entire lung
Klinisk navn: Atelectasis
Collapse of part of a lung associated with absence of inflation (air) of that part.
Resumé
- Også kaldet
- Pulmonary atelectasis
- Kropssystem
- Abnormality of the respiratory system
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/atelectasis.json"
page <- fromJSON(url)
page$trait$nameLæs de gener, der er knyttet til Partial or complete collapse of part or entire lung, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test34 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.
- Primary Ciliary DyskinesiaReads 48 of these genesCFAP54DNAI1CCDC39CCDC40CCNOCFAP221About this report →
- Tuberous SclerosisReads 2 of these genesTSC1TSC2About this report →
- Surfactant Metabolism DysfunctionReads 3 of these genesABCA3SFTPBSFTPCAbout this report →
- 22q11.2 Deletion SyndromeReads 1 of these genesTBX1About this report →
Show 30 more reports
- Dent Disease and Lowe SyndromeReads 1 of these genesOCRLAbout this report →
- STAT1 and STAT3 Gain-of-Function DiseaseReads 1 of these genesSTAT3About this report →
- EBV-Driven Lymphoproliferation and CARD11 Immune DysregulationReads 1 of these genesIKZF2About this report →
- Chronic Granulomatous DiseaseReads 1 of these genesCYBBAbout this report →
- Spinal Muscular AtrophyReads 2 of these genesHSPB8ASAH1About this report →
- Hyper-IgE SyndromeReads 1 of these genesSTAT3About this report →
- Waardenburg SyndromeReads 1 of these genesPAX3About this report →
- Limb-Girdle Muscular DystrophyReads 2 of these genesLAMA2PLECAbout this report →
- Other Inborn Errors of ImmunityReads 5 of these genesCYBBIKZF2STAT3C1QBTBX1About this report →
- Inherited Platelet Function DisordersReads 1 of these genesGP1BBAbout this report →
- Male InfertilityReads 2 of these genesDNAH1SPEF2About this report →
- Heterotaxy & Laterality DefectsReads 1 of these genesDAW1About this report →
- Severe Congenital NeutropeniaReads 1 of these genesCXCR4About this report →
- Myofibrillar MyopathiesReads 1 of these genesHSPB8About this report →
- Cutis LaxaReads 1 of these genesLTBP4About this report →
- Inherited Complement and Properdin DeficienciesReads 1 of these genesC1QBAbout this report →
- Epidermolysis BullosaReads 1 of these genesPLECAbout this report →
- Retinitis PigmentosaReads 2 of these genesOFD1RPGRAbout this report →
- Congenital HypothyroidismReads 1 of these genesNKX2-1About this report →
- Autoimmune DiseaseReads 1 of these genesSTAT3About this report →
- Ehlers-Danlos SyndromeReads 1 of these genesB3GALT6About this report →
- Congenital Myasthenic SyndromeReads 1 of these genesPLECAbout this report →
- Congenital Muscular DystrophiesReads 1 of these genesLAMA2About this report →
- Inherited ThrombocytopeniasReads 1 of these genesGP1BBAbout this report →
- Joubert Syndrome And Related DisordersReads 1 of these genesOFD1About this report →
- Lysosomal Storage DiseaseReads 1 of these genesASAH1About this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesHSPB8About this report →
- Hearing Loss and DeafnessReads 1 of these genesIKZF2About this report →
- Congenital Disorders of GlycosylationReads 1 of these genesB3GALT6About this report →
- Intellectual DisabilityReads 1 of these genesJMJD1CAbout this report →
Læs de gener, der er knyttet til Partial or complete collapse of part or entire lung, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test87 gener knyttet til Partial or complete collapse of part or entire lung
Ændringer i disse gener forårsager sjældne tilstande, hvor Partial or complete collapse of part or entire lung 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 |
|---|---|---|
| CFAP54cilia and flagella associated protein 54 | Altid | I 1 tilstand |
| CYBBcytochrome b-245 beta chain | Altid | I 1 tilstand |
| DNAI1dynein axonemal intermediate chain 1 | Altid | I 2 tilstande |
| ESAMendothelial cell adhesion molecule | Altid | I 1 tilstand |
| GINS3GINS complex subunit 3 | Altid | I 1 tilstand |
| HSPB8heat shock protein family B (small) member 8 | Altid | I 1 tilstand |
| IKZF2IKAROS family zinc finger 2 | Altid | I 1 tilstand |
| STAT3signal transducer and activator of transcription 3 | Meget ofte (80–99 %) | I 1 tilstand |
| ABCA3ATP binding cassette subfamily A member 3 | Ofte (30–79 %) | I 1 tilstand |
| C1QBcomplement C1q B chain | Ofte (30–79 %) | I 1 tilstand |
| LTBP4latent transforming growth factor beta binding protein 4 | Ofte (30–79 %) | I 1 tilstand |
| PAX3paired box 3 | Ofte (30–79 %) | I 1 tilstand |
| RIPK4receptor interacting serine/threonine kinase 4 | Ofte (30–79 %) | I 1 tilstand |
| SFTPBsurfactant protein B | Ofte (30–79 %) | I 1 tilstand |
| SFTPCsurfactant protein C | Ofte (30–79 %) | I 1 tilstand |
| TSC1TSC complex subunit 1 | Ofte (30–79 %) | I 1 tilstand |
| TSC2TSC complex subunit 2 | Ofte (30–79 %) | I 1 tilstand |
| AGR2anterior gradient 2, protein disulphide isomerase family member | Nogle gange (5–29 %) | I 1 tilstand |
| ARVCFARVCF delta catenin family member | Nogle gange (5–29 %) | I 1 tilstand |
| ASAH1N-acylsphingosine amidohydrolase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| B3GALT6beta-1,3-galactosyltransferase 6 | Nogle gange (5–29 %) | I 1 tilstand |
| BRWD1bromodomain and WD repeat domain containing 1 | Nogle gange (5–29 %) | I 1 tilstand |
| CCDC39coiled-coil domain 39 molecular ruler complex subunit | Nogle gange (5–29 %) | I 1 tilstand |
| CCDC40coiled-coil domain 40 molecular ruler complex subunit | Nogle gange (5–29 %) | I 1 tilstand |
| CCNOcyclin O | Nogle gange (5–29 %) | I 2 tilstande |
| CFAP221cilia and flagella associated protein 221 | Nogle gange (5–29 %) | I 1 tilstand |
| CFAP298cilia and flagella associated protein 298 | Nogle gange (5–29 %) | I 1 tilstand |
| CFAP300cilia and flagella associated protein 300 | Nogle gange (5–29 %) | I 1 tilstand |
| CFAP74cilia and flagella associated protein 74 | Nogle gange (5–29 %) | I 1 tilstand |
| CLXNcalaxin | Nogle gange (5–29 %) | I 1 tilstand |
| COMTcatechol-O-methyltransferase | Nogle gange (5–29 %) | I 1 tilstand |
| DAW1dynein assembly factor with WD repeats 1 | Nogle gange (5–29 %) | I 1 tilstand |
| DNAAF1dynein axonemal assembly factor 1 | Nogle gange (5–29 %) | I 1 tilstand |
| DNAAF11dynein axonemal assembly factor 11 | Nogle gange (5–29 %) | I 1 tilstand |
| DNAAF19dynein axonemal assembly factor 19 | Nogle gange (5–29 %) | I 1 tilstand |
| DNAAF2dynein axonemal assembly factor 2 | Nogle gange (5–29 %) | I 1 tilstand |
| DNAAF3dynein axonemal assembly factor 3 | Nogle gange (5–29 %) | I 1 tilstand |
| DNAAF4dynein axonemal assembly factor 4 | Nogle gange (5–29 %) | I 1 tilstand |
| DNAAF5dynein axonemal assembly factor 5 | Nogle gange (5–29 %) | I 1 tilstand |
| DNAAF6dynein axonemal assembly factor 6 | Nogle gange (5–29 %) | I 1 tilstand |
Vis 47 gener mere
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| DNAH1dynein axonemal heavy chain 1 | Nogle gange (5–29 %) | I 1 tilstand |
| DNAH11dynein axonemal heavy chain 11 | Nogle gange (5–29 %) | I 1 tilstand |
| DNAH5dynein axonemal heavy chain 5 | Nogle gange (5–29 %) | I 1 tilstand |
| DNAH7dynein axonemal heavy chain 7 | Nogle gange (5–29 %) | I 1 tilstand |
| DNAH9dynein axonemal heavy chain 9 | Nogle gange (5–29 %) | I 1 tilstand |
| DNAI2dynein axonemal intermediate chain 2 | Nogle gange (5–29 %) | I 1 tilstand |
| DNAJB13DnaJ heat shock protein family (Hsp40) member B13 | Nogle gange (5–29 %) | I 1 tilstand |
| DNAL1dynein axonemal light chain 1 | Nogle gange (5–29 %) | I 1 tilstand |
| DRC1dynein regulatory complex subunit 1 | Nogle gange (5–29 %) | I 2 tilstande |
| DRC2dynein regulatory complex subunit 2 | Nogle gange (5–29 %) | I 1 tilstand |
| DRC4dynein regulatory complex subunit 4 | Nogle gange (5–29 %) | I 2 tilstande |
| FOXJ1forkhead box J1 | Nogle gange (5–29 %) | I 1 tilstand |
| GAS2L2growth arrest specific 2 like 2 | Nogle gange (5–29 %) | I 1 tilstand |
| GP1BBglycoprotein Ib platelet subunit beta | Nogle gange (5–29 %) | I 1 tilstand |
| HIRAhistone cell cycle regulator | Nogle gange (5–29 %) | I 1 tilstand |
| HYDINHYDIN axonemal central pair apparatus protein | Nogle gange (5–29 %) | I 1 tilstand |
| JMJD1Cjumonji domain containing 1C | Nogle gange (5–29 %) | I 1 tilstand |
| LAMA2laminin subunit alpha 2 | Nogle gange (5–29 %) | I 1 tilstand |
| LRRC56leucine rich repeat containing 56 | Nogle gange (5–29 %) | I 1 tilstand |
| MCIDASmulticiliate differentiation and DNA synthesis associated cell cycle protein | Nogle gange (5–29 %) | I 1 tilstand |
| NEK10NIMA related kinase 10 | Nogle gange (5–29 %) | I 1 tilstand |
| NKX2-1NK2 homeobox 1 | Nogle gange (5–29 %) | I 1 tilstand |
| NME5NME/NM23 family member 5 | Nogle gange (5–29 %) | I 1 tilstand |
| NME8NME/NM23 family member 8 | Nogle gange (5–29 %) | I 1 tilstand |
| OCRLOCRL inositol polyphosphate-5-phosphatase | Nogle gange (5–29 %) | I 1 tilstand |
| ODAD1outer dynein arm docking complex subunit 1 | Nogle gange (5–29 %) | I 2 tilstande |
| ODAD2outer dynein arm docking complex subunit 2 | Nogle gange (5–29 %) | I 1 tilstand |
| ODAD3outer dynein arm docking complex subunit 3 | Nogle gange (5–29 %) | I 1 tilstand |
| ODAD4outer dynein arm docking complex subunit 4 | Nogle gange (5–29 %) | I 1 tilstand |
| OFD1OFD1 centriole and centriolar satellite protein | Nogle gange (5–29 %) | I 1 tilstand |
| RPGRretinitis pigmentosa GTPase regulator | Nogle gange (5–29 %) | I 2 tilstande |
| RREB1ras responsive element binding protein 1 | Nogle gange (5–29 %) | I 1 tilstand |
| RSPH1radial spoke head component 1 | Nogle gange (5–29 %) | I 1 tilstand |
| RSPH3radial spoke head 3 | Nogle gange (5–29 %) | I 1 tilstand |
| RSPH4Aradial spoke head component 4A | Nogle gange (5–29 %) | I 1 tilstand |
| RSPH9radial spoke head component 9 | Nogle gange (5–29 %) | I 1 tilstand |
| SEC24CSEC24 homolog C, COPII component | Nogle gange (5–29 %) | I 1 tilstand |
| SPAG1sperm associated antigen 1 | Nogle gange (5–29 %) | I 1 tilstand |
| SPEF2sperm flagellar and cilia associated 2 | Nogle gange (5–29 %) | I 1 tilstand |
| STK36serine/threonine kinase 36 | Nogle gange (5–29 %) | I 1 tilstand |
| TBX1T-box transcription factor 1 | Nogle gange (5–29 %) | I 2 tilstande |
| TTC12tetratricopeptide repeat domain 12 | Nogle gange (5–29 %) | I 1 tilstand |
| UFD1ubiquitin recognition factor in ER associated degradation 1 | Nogle gange (5–29 %) | I 1 tilstand |
| ZMYND10zinc finger MYND-type containing 10 | Nogle gange (5–29 %) | I 1 tilstand |
| CXCR4C-X-C motif chemokine receptor 4 | Sjældent (1–4%) | I 1 tilstand |
| PLECplectin | Sjældent (1–4%) | I 1 tilstand |
| TP73tumor protein p73 | 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.
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 2026.10.17-8666dff2.
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