Tulajdonság
Pneumonia
Inflammation of any part of the lung parenchyma.
Összefoglaló
Ez az oldal adatként
Adja hozzá a .json végződést az oldal címéhez, vagy kérjen application/json típust, hogy JSON-ként olvassa be.
library(jsonlite)
url <- "https://dantelabs.com/traits/pneumonia.json"
page <- fromJSON(url)
page$trait$nameOlvassa el a(z) Pneumonia nevű génhez kapcsolódó információkat, valamint a genomja többi részét egyetlen teszttel.
449 $-tólIngyenes szállítás · Eredmények 6–8 hét alatt
Kérem a Genome Testemet78 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.
- Other Inborn Errors of ImmunityReads 39 of these genesCASP8DCLRE1CICOSLGIKBKGIRF1ITPR3About this report →
- Severe Combined ImmunodeficiencyReads 15 of these genesDCLRE1CJAK3NHEJ1RAG1RAG2IL2RGAbout this report →
- Inherited Congenital Heart DefectsReads 7 of these genesACTC1GATA4GATA6MYH6NKX2-5TBX20About this report →
- Type I InterferonopathiesReads 5 of these genesPSMB10PSMB9IFIH1TREX1ACP5About this report →
Show 74 more reports
- Shwachman-Diamond SyndromeReads 2 of these genesEFL1SBDSAbout this report →
- Surfactant Metabolism DysfunctionReads 3 of these genesABCA3SFTPBSFTPCAbout this report →
- Severe Congenital NeutropeniaReads 4 of these genesCLPBCXCR4ELANEGFI1About this report →
- IPEX Syndrome and Other TregopathiesReads 3 of these genesLRBACTLA4FOXP3About this report →
- Autoimmune DiseaseReads 5 of these genesCASP8CTLA4ZAP70TREX1FOXP3About this report →
- Bloom SyndromeReads 1 of these genesBLMAbout this report →
- CHARGE SyndromeReads 1 of these genesCHD7About this report →
- Mucopolysaccharidosis Type VI (Maroteaux-Lamy Syndrome)Reads 1 of these genesARSBAbout this report →
- POLR3A-Related DisorderReads 1 of these genesPOLR3AAbout this report →
- Purine Nucleoside Phosphorylase DeficiencyReads 1 of these genesPNPAbout this report →
- Very Long Chain Acyl-Coa Dehydrogenase DeficiencyReads 1 of these genesACADVLAbout this report →
- Vici SyndromeReads 1 of these genesEPG5About this report →
- X-linked Autoinflammatory DiseaseReads 1 of these genesIKBKGAbout this report →
- Common Variable Immunodeficiency (Monogenic CVID)Reads 3 of these genesLRBASEC61A1ICOSAbout this report →
- Mendelian Susceptibility to Mycobacterial Disease (MSMD)Reads 3 of these genesIL12RB1IFNGR1IRF8About this report →
- Congenital MyopathiesReads 4 of these genesACTA1MTM1SELENONRYR1About this report →
- Rare Monogenic Autoinflammatory DiseasesReads 5 of these genesPSMB10PSMB9IFIH1TREX1ACP5About this report →
- Alpha-Mannosidosis and Other GlycoproteinosesReads 2 of these genesCTSAMAN2B1About this report →
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 2 of these genesCASP8CTLA4About this report →
- Hyper-IgE SyndromeReads 2 of these genesDOCK8SPINK5About this report →
- Aicardi-Goutieres SyndromeReads 2 of these genesIFIH1TREX1About this report →
- Activated PI3K-Delta Syndrome (APDS)Reads 1 of these genesPIK3CDAbout this report →
- Encephalopathy due to Mitochondrial and Peroxisomal Fission DefectReads 1 of these genesDNM1LAbout this report →
- Malignant Hyperthermia SusceptibilityReads 1 of these genesRYR1About this report →
- WHIM SyndromeReads 1 of these genesCXCR4About this report →
- Epidermolysis BullosaReads 3 of these genesLAMA3LAMB3LAMC2About this report →
- EBV-Driven Lymphoproliferation and CARD11 Immune DysregulationReads 1 of these genesCARD11About this report →
- Immuno-Osseous DysplasiasReads 1 of these genesRMRPAbout this report →
- Leukocyte Adhesion DeficiencyReads 1 of these genesSLC35C1About this report →
- Tetralogy of FallotReads 1 of these genesNKX2-5About this report →
- Primary Ciliary DyskinesiaReads 4 of these genesCFAP54MCIDASDNAI1DNAI2About this report →
- DNA Repair DiseaseReads 3 of these genesDCLRE1CFANCFNBNAbout this report →
- Other Inherited LeukodystrophiesReads 4 of these genesPOLR3AIFIH1TREX1ALDH3A2About this report →
- Neonatal Diabetes MellitusReads 2 of these genesGATA4GATA6About this report →
- Autosomal Dominant Tubulointerstitial Kidney DiseaseReads 1 of these genesSEC61A1About this report →
- Chronic Mucocutaneous CandidiasisReads 1 of these genesIL17RAAbout this report →
- Dilated CardiomyopathyReads 3 of these genesSGCGACTC1TBX20About this report →
- Dyskeratosis CongenitaReads 2 of these genesDNMT3BZBTB24About this report →
- Cornelia de Lange SyndromeReads 1 of these genesNIPBLAbout this report →
- Rare Inherited Bone Marrow Failure SyndromesReads 1 of these genesDNAJC21About this report →
- Syndromic and Metabolic CardiomyopathiesReads 1 of these genesNKX2-5About this report →
- Systemic Lupus ErythematosusReads 1 of these genesTREX1About this report →
- Lysosomal Storage DiseaseReads 3 of these genesCTSAARSBMAN2B1About this report →
- Hypertrophic CardiomyopathyReads 3 of these genesACADVLACTC1MYH6About this report →
- Left Ventricular NoncompactionReads 1 of these genesACTC1About this report →
- Inherited Neurodegenerative DisordersReads 7 of these genesDNM1LRTN2POLR3ARNF168IFIH1TREX1About this report →
- Diabetes MellitusReads 2 of these genesGATA4GATA6About this report →
- Osteogenesis ImperfectaReads 2 of these genesPOLR3AIFIH1About this report →
- Hemolytic Uremic Syndrome, Interstitial NephritisReads 1 of these genesCFBAbout this report →
- Agammaglobulinaemia (XLA and Autosomal Forms)Reads 1 of these genesBTKAbout this report →
- Long QT SyndromeReads 1 of these genesCACNA1CAbout this report →
- Congenital Disorders of GlycosylationReads 3 of these genesPIGASLC35A1SLC35C1About this report →
- Hereditary Optic NeuropathyReads 1 of these genesDNM1LAbout this report →
- Myofibrillar MyopathiesReads 1 of these genesRYR1About this report →
- OsteopetrosisReads 1 of these genesTCIRG1About this report →
- Fatty Acid Oxidation & Carnitine Cycle DisordersReads 1 of these genesACADVLAbout this report →
- Amelogenesis ImperfectaReads 1 of these genesLAMB3About this report →
- Ectodermal DysplasiasReads 1 of these genesIKBKGAbout this report →
- Fanconi AnemiaReads 1 of these genesFANCFAbout this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 1 of these genesGATA4About this report →
- Charcot-Marie-Tooth DiseaseReads 2 of these genesITPR3RTN2About this report →
- Congenital HypothyroidismReads 1 of these genesNKX2-5About this report →
- GPI Anchor Biosynthesis DefectsReads 1 of these genesPIGAAbout this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 1 of these genesPOLR3AAbout this report →
- Intellectual DisabilityReads 3 of these genesKDM6BCREBBPEP300About this report →
- VitreoretinopathyReads 1 of these genesIKBKGAbout this report →
- Congenital Muscular DystrophiesReads 1 of these genesSELENONAbout this report →
- Thyroid CancerReads 1 of these genesNKX2-5About this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesSGCGAbout this report →
- Hypogonadotropic HypogonadismReads 1 of these genesCHD7About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesRNF168About this report →
- Rare Hereditary Peripheral NeuropathiesReads 2 of these genesITPR3RTN2About this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesRTN2About this report →
- Epilepsy (Full Panel)Reads 1 of these genesPIGAAbout this report →
Olvassa el a(z) Pneumonia nevű génhez kapcsolódó információkat, valamint a genomja többi részét egyetlen teszttel.
449 $-tólIngyenes szállítás · Eredmények 6–8 hét alatt
Kérem a Genome Testemet114 gén kapcsolódik ehhez: Pneumonia
Ezeknek a géneknek a változásai olyan ritka betegségeket okoznak, amelyekben előfordul a(z) Pneumonia. A tulajdonsággal rendelkező emberek többségének nincs ezek közül egyik betegsége sem, a listán szereplő gének pedig semmit nem mondanak el senki saját genomjáról.
| Gén | Milyen gyakran fordul elő | Betegségek |
|---|---|---|
| CASP8caspase 8 | Mindig | 1 betegségben |
| CFAP54cilia and flagella associated protein 54 | Mindig | 1 betegségben |
| CILK1ciliogenesis associated kinase 1 | Mindig | 1 betegségben |
| COPZ1coat protein complex I subunit zeta 1 | Mindig | 1 betegségben |
| CTSAcathepsin A | Mindig | 1 betegségben |
| DCLRE1CDNA cross-link repair 1C | Mindig | 3 betegségben |
| DNM1Ldynamin 1L | Mindig | 1 betegségben |
| EPG5ectopic P-granules 5 autophagy tethering factor | Mindig | 1 betegségben |
| FANCFFA complementation group F | Mindig | 1 betegségben |
| ICOSLGinducible T cell costimulator ligand | Mindig | 1 betegségben |
| IKBKGinhibitor of nuclear factor kappa B kinase regulatory subunit gamma | Mindig | 1 betegségben |
| IRF1interferon regulatory factor 1 | Mindig | 1 betegségben |
| ITPR3inositol 1,4,5-trisphosphate receptor type 3 | Mindig | 1 betegségben |
| JAK3Janus kinase 3 | Mindig | 1 betegségben |
| KDM6Blysine demethylase 6B | Mindig | 1 betegségben |
| LRBALPS responsive beige-like anchor protein | Mindig | 1 betegségben |
| MCIDASmulticiliate differentiation and DNA synthesis associated cell cycle protein | Mindig | 1 betegségben |
| MDGA2MAM domain containing glycosylphosphatidylinositol anchor 2 | Mindig | 1 betegségben |
| NBNnibrin | Mindig | 1 betegségben |
| NHEJ1non-homologous end joining factor 1 | Mindig | 1 betegségben |
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Mindig | 1 betegségben |
| PPFIA3PPFI scaffold protein A3 | Mindig | 1 betegségben |
| RAG1recombination activating 1 | Mindig | 3 betegségben |
| RAG2recombination activating 2 | Mindig | 3 betegségben |
| RELREL proto-oncogene, NF-kB subunit | Mindig | 1 betegségben |
| RTN2reticulon 2 | Mindig | 1 betegségben |
| SEC61A1SEC61 translocon subunit alpha 1 | Mindig | 1 betegségben |
| DOCK8dedicator of cytokinesis 8 | Nagyon gyakran (80–99%) | 1 betegségben |
| IL2RGinterleukin 2 receptor subunit gamma | Nagyon gyakran (80–99%) | 4 betegségben |
| SLC35A1solute carrier family 35 member A1 | Nagyon gyakran (80–99%) | 1 betegségben |
| ACTA1actin alpha 1, skeletal muscle | Gyakran (30–79%) | 1 betegségben |
| ADAadenosine deaminase | Gyakran (30–79%) | 2 betegségben |
| ARSBarylsulfatase B | Gyakran (30–79%) | 1 betegségben |
| CARD11caspase recruitment domain family member 11 | Gyakran (30–79%) | 1 betegségben |
| CHD7chromodomain helicase DNA binding protein 7 | Gyakran (30–79%) | 1 betegségben |
| CLPBClpB family mitochondrial disaggregase | Gyakran (30–79%) | 1 betegségben |
| CTLA4cytotoxic T-lymphocyte associated protein 4 | Gyakran (30–79%) | 1 betegségben |
| CXCR4C-X-C motif chemokine receptor 4 | Gyakran (30–79%) | 1 betegségben |
| ELANEelastase, neutrophil expressed | Gyakran (30–79%) | 1 betegségben |
| FCGR3BFc gamma receptor IIIb | Gyakran (30–79%) | 1 betegségben |
További 74 gén megjelenítése
| Gén | Milyen gyakran fordul elő | Betegségek |
|---|---|---|
| FOXN1forkhead box N1 | Gyakran (30–79%) | 2 betegségben |
| GFI1growth factor independent 1 transcriptional repressor | Gyakran (30–79%) | 1 betegségben |
| IL7Rinterleukin 7 receptor | Gyakran (30–79%) | 2 betegségben |
| MAN2B1mannosidase alpha class 2B member 1 | Gyakran (30–79%) | 2 betegségben |
| MTM1myotubularin 1 | Gyakran (30–79%) | 1 betegségben |
| NUDCD3NudC domain containing 3 | Gyakran (30–79%) | 1 betegségben |
| POLR3ARNA polymerase III subunit A | Gyakran (30–79%) | 1 betegségben |
| PSMB10proteasome 20S subunit beta 10 | Gyakran (30–79%) | 1 betegségben |
| PSMB9proteasome 20S subunit beta 9 | Gyakran (30–79%) | 1 betegségben |
| RFX5regulatory factor X5 | Gyakran (30–79%) | 1 betegségben |
| RMRPRNA component of mitochondrial RNA processing endoribonuclease | Gyakran (30–79%) | 1 betegségben |
| RNF168ring finger protein 168 | Gyakran (30–79%) | 1 betegségben |
| SELENONselenoprotein N | Gyakran (30–79%) | 1 betegségben |
| SPINK5serine peptidase inhibitor Kazal type 5 | Gyakran (30–79%) | 1 betegségben |
| SRP19signal recognition particle 19 | Gyakran (30–79%) | 1 betegségben |
| SYKspleen associated tyrosine kinase | Gyakran (30–79%) | 1 betegségben |
| TCIRG1T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 | Gyakran (30–79%) | 1 betegségben |
| ZAP70zeta chain of T cell receptor associated protein kinase 70 | Gyakran (30–79%) | 2 betegségben |
| ABCA3ATP binding cassette subfamily A member 3 | Néha (5–29%) | 1 betegségben |
| BLMBLM RecQ like helicase | Néha (5–29%) | 1 betegségben |
| BORCS5BLOC-1 related complex subunit 5 | Néha (5–29%) | 1 betegségben |
| CACNA1Ccalcium voltage-gated channel subunit alpha1 C | Néha (5–29%) | 1 betegségben |
| CD247CD247 molecule | Néha (5–29%) | 1 betegségben |
| CD3DCD3 delta subunit of T-cell receptor complex | Néha (5–29%) | 1 betegségben |
| CD3ECD3 epsilon subunit of T-cell receptor complex | Néha (5–29%) | 1 betegségben |
| CREBBPCREB binding lysine acetyltransferase | Néha (5–29%) | 2 betegségben |
| DNAJC21DnaJ heat shock protein family (Hsp40) member C21 | Néha (5–29%) | 1 betegségben |
| EFL1elongation factor like GTPase 1 | Néha (5–29%) | 1 betegségben |
| EP300EP300 lysine acetyltransferase | Néha (5–29%) | 1 betegségben |
| FOCADfocadhesin | Néha (5–29%) | 1 betegségben |
| IFIH1interferon induced with helicase C domain 1 | Néha (5–29%) | 1 betegségben |
| IGHG2immunoglobulin heavy constant gamma 2 (G2m marker) | Néha (5–29%) | 1 betegségben |
| IGKCimmunoglobulin kappa constant | Néha (5–29%) | 1 betegségben |
| IL12RB1interleukin 12 receptor subunit beta 1 | Néha (5–29%) | 1 betegségben |
| IL17RAinterleukin 17 receptor A | Néha (5–29%) | 1 betegségben |
| LAMA3laminin subunit alpha 3 | Néha (5–29%) | 1 betegségben |
| LAMB3laminin subunit beta 3 | Néha (5–29%) | 1 betegségben |
| LAMC2laminin subunit gamma 2 | Néha (5–29%) | 1 betegségben |
| RYR1ryanodine receptor 1 | Néha (5–29%) | 1 betegségben |
| SBDSSBDS ribosome maturation factor | Néha (5–29%) | 1 betegségben |
| SFTPBsurfactant protein B | Néha (5–29%) | 1 betegségben |
| SFTPCsurfactant protein C | Néha (5–29%) | 1 betegségben |
| SGCGsarcoglycan gamma | Néha (5–29%) | 1 betegségben |
| TREX1three prime repair exonuclease 1 | Néha (5–29%) | 1 betegségben |
| ZNF699zinc finger protein 699 | Néha (5–29%) | 1 betegségben |
| ACADVLacyl-CoA dehydrogenase very long chain | Ritkán (1–4%) | 1 betegségben |
| ACP5acid phosphatase 5, tartrate resistant | Ritkán (1–4%) | 2 betegségben |
| ACTC1actin alpha cardiac muscle 1 | Ritkán (1–4%) | 1 betegségben |
| ALDH3A2aldehyde dehydrogenase 3 family member A2 | Ritkán (1–4%) | 1 betegségben |
| CITED2Cbp/p300 interacting transactivator with ED-rich tail 2 | Ritkán (1–4%) | 1 betegségben |
| FOXP3forkhead box P3 | Ritkán (1–4%) | 1 betegségben |
| GATA4GATA binding protein 4 | Ritkán (1–4%) | 1 betegségben |
| GATA6GATA binding protein 6 | Ritkán (1–4%) | 1 betegségben |
| MYH6myosin heavy chain 6 | Ritkán (1–4%) | 1 betegségben |
| NKX2-5NK2 homeobox 5 | Ritkán (1–4%) | 1 betegségben |
| TBX20T-box transcription factor 20 | Ritkán (1–4%) | 1 betegségben |
| TLL1tolloid like 1 | Ritkán (1–4%) | 1 betegségben |
| BTKBruton tyrosine kinase | Nincs rögzítve | 1 betegségben |
| CFBcomplement factor B | Nincs rögzítve | 1 betegségben |
| DNAI1dynein axonemal intermediate chain 1 | Nincs rögzítve | 1 betegségben |
| DNAI2dynein axonemal intermediate chain 2 | Nincs rögzítve | 1 betegségben |
| DNMT3BDNA methyltransferase 3 beta | Nincs rögzítve | 1 betegségben |
| ICOSinducible T cell costimulator | Nincs rögzítve | 1 betegségben |
| IFNGR1interferon gamma receptor 1 | Nincs rögzítve | 1 betegségben |
| IRF8interferon regulatory factor 8 | Nincs rögzítve | 1 betegségben |
| KNSTRNkinetochore localized astrin (SPAG5) binding protein | Nincs rögzítve | 1 betegségben |
| LTBP3latent transforming growth factor beta binding protein 3 | Nincs rögzítve | 1 betegségben |
| NIPBLNIPBL cohesin loading factor | Nincs rögzítve | 1 betegségben |
| PIK3CDphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | Nincs rögzítve | 1 betegségben |
| PNPpurine nucleoside phosphorylase | Nincs rögzítve | 1 betegségben |
| RANBP2RAN binding protein 2 | Nincs rögzítve | 1 betegségben |
| SLC35C1solute carrier family 35 member C1 | Nincs rögzítve | 1 betegségben |
| SREBF1sterol regulatory element binding transcription factor 1 | Nincs rögzítve | 1 betegségben |
| ZBTB24zinc finger and BTB domain containing 24 | Nincs rögzítve | 1 betegségben |
Az, hogy milyen gyakran fordul elő a gén valamelyik állapotával élő emberek körében (a leggyakoribb érték, ahogyan a Human Phenotype Ontology rögzíti). Ezek az oldalak tulajdonságokat és az azok mögött álló kutatásokat ismertetik; nem diagnózist jelentenek. A tünetekkel kapcsolatban orvoshoz vagy genetikai tanácsadóhoz érdemes fordulni.
Szűkebb tulajdonságok
Tágabb tulajdonságok
Forrás
- Human Phenotype Ontology, 2026-09-01 kiadás: a tulajdonság, a nevei, a definíciója és a hozzá kapcsolt gének. További információ: hpo.jax.org.
- Adatkiadás: 2026.10.18-8b139e39.
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Ingyenes szállítás · Eredmények 6–8 hét alatt
