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Chronic infections of the middle ear
Klinisk navn: Chronic otitis media
Chronic otitis media refers to fluid, swelling, or infection of the middle ear that does not heal and may cause permanent damage to the ear.
Resumé
- Også kaldet
- Chronic middle ear infection, Otitis media, chronic
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Tilføj .json til sidens adresse, eller bed om application/json, for at læse den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/chronic-otitis-media.json"
page <- fromJSON(url)
page$trait$nameChronic infections of the middle earHP:0000389
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Læs de gener, der er knyttet til Chronic infections of the middle ear, og resten af dit genom, med én test.
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Bestil min Genome Test53 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 47 of these genesDNAAF2DNAAF6DNAI1DNAI2DNAL1ODAD4About this report →
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- Other Inborn Errors of ImmunityReads 22 of these genesAK2BLNKBTKCD79ACD79BDOCK8About this report →
- Activated PI3K-Delta Syndrome (APDS)Reads 2 of these genesPIK3CDPIK3R1About this report →
Show 49 more reports
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- Catel-Manzke SyndromeReads 1 of these genesTGDSAbout this report →
- Fragile X SyndromeReads 1 of these genesFMR1About this report →
- OFD1-Related CiliopathyReads 1 of these genesOFD1About this report →
- PIK3R1-Related DisordersReads 1 of these genesPIK3R1About this report →
- Hereditary Orofacial CleftingReads 2 of these genesIRF6MSX1About this report →
- Hyper-IgE SyndromeReads 2 of these genesDOCK8STAT3About this report →
- Cleidocranial DysplasiaReads 1 of these genesRUNX2About this report →
- Dent Disease and Lowe SyndromeReads 1 of these genesOCRLAbout this report →
- STAT1 and STAT3 Gain-of-Function DiseaseReads 1 of these genesSTAT3About this report →
- Wiskott-Aldrich Syndrome SpectrumReads 1 of these genesWASAbout this report →
- Syndromic CraniosynostosisReads 3 of these genesFGFR2IL11RAKAT6AAbout this report →
- Myelodysplastic Syndrome (MDS)Reads 1 of these genesGATA2About this report →
- Van der Woude and Popliteal Pterygium Syndromes (IRF6)Reads 1 of these genesIRF6About this report →
- Severe Combined ImmunodeficiencyReads 3 of these genesAK2CARMIL2FOXN1About this report →
- Intellectual DisabilityReads 8 of these genesAHDC1JMJD1CRAI1TAF1ANKRD11KAT6AAbout this report →
- Inherited Predisposition to Myeloid Blood CancersReads 1 of these genesGATA2About this report →
- Overgrowth Syndromes (Sotos, Weaver, Tatton-Brown-Rahman, Malan)Reads 1 of these genesNSD1About this report →
- Ectodermal DysplasiasReads 2 of these genesNECTIN1TP63About this report →
- Male InfertilityReads 3 of these genesDNAH1FKBP6SPEF2About this report →
- GPI Anchor Biosynthesis DefectsReads 2 of these genesPIGHPIGGAbout this report →
- Autoimmune DiseaseReads 2 of these genesSTAT3CTLA4About this report →
- Chronic Granulomatous DiseaseReads 1 of these genesNCF1About this report →
- Alpha-Mannosidosis and Other GlycoproteinosesReads 1 of these genesAGAAbout this report →
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 1 of these genesCTLA4About this report →
- Hypodontia and AnodontiaReads 1 of these genesMSX1About this report →
- Inherited Predisposition to Acute Myeloid LeukaemiaReads 1 of these genesGATA2About this report →
- IPEX Syndrome and Other TregopathiesReads 1 of these genesCTLA4About this report →
- Inherited ThrombocytopeniasReads 2 of these genesWASGP1BBAbout this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 1 of these genesNSD1About this report →
- Inherited Platelet Function DisordersReads 1 of these genesGP1BBAbout this report →
- Heterotaxy & Laterality DefectsReads 1 of these genesDAW1About this report →
- Severe Congenital NeutropeniaReads 1 of these genesWASAbout this report →
- Inherited Congenital Heart DefectsReads 1 of these genesELNAbout this report →
- Female InfertilityReads 2 of these genesFMR1TP63About this report →
- Complex Cortical Dysplasia and Frontoparietal PolymicrogyriaReads 1 of these genesAPC2About this report →
- Cutis LaxaReads 1 of these genesELNAbout this report →
- Retinitis PigmentosaReads 2 of these genesOFD1RPGRAbout this report →
- Lissencephaly Spectrum DisordersReads 1 of these genesAPC2About this report →
- Congenital Disorders of GlycosylationReads 2 of these genesPGM3PIGGAbout this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesTAF1About this report →
- Joubert Syndrome And Related DisordersReads 1 of these genesOFD1About this report →
- Epilepsy (Full Panel)Reads 2 of these genesSLC25A12CPLX1About this report →
- Lysosomal Storage DiseaseReads 1 of these genesAGAAbout this report →
- Hypertrophic CardiomyopathyReads 1 of these genesNSD1About this report →
- Inherited Neurodegenerative DisordersReads 2 of these genesFMR1LETM1About this report →
- Primary Mitochondrial DiseaseReads 1 of these genesDNAJC30About this report →
Læs de gener, der er knyttet til Chronic infections of the middle ear, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test142 gener knyttet til Chronic infections of the middle ear
Ændringer i disse gener forårsager sjældne tilstande, hvor Chronic infections of the middle ear 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 |
|---|---|---|
| AHDC1AT-hook DNA binding motif containing 1 | Altid | I 1 tilstand |
| BORCS8BLOC-1 related complex subunit 8 | Altid | I 1 tilstand |
| DNAAF2dynein axonemal assembly factor 2 | Altid | I 2 tilstande |
| DNAAF6dynein axonemal assembly factor 6 | Altid | I 2 tilstande |
| DNAI1dynein axonemal intermediate chain 1 | Altid | I 2 tilstande |
| DNAI2dynein axonemal intermediate chain 2 | Altid | I 2 tilstande |
| DNAL1dynein axonemal light chain 1 | Altid | I 2 tilstande |
| ODAD4outer dynein arm docking complex subunit 4 | Altid | I 2 tilstande |
| AK2adenylate kinase 2 | Meget ofte (80–99 %) | I 1 tilstand |
| BLNKB cell linker | Meget ofte (80–99 %) | I 1 tilstand |
| BTKBruton tyrosine kinase | Meget ofte (80–99 %) | I 1 tilstand |
| CD79ACD79a molecule | Meget ofte (80–99 %) | I 1 tilstand |
| CD79BCD79b molecule | Meget ofte (80–99 %) | I 1 tilstand |
| DOCK8dedicator of cytokinesis 8 | Meget ofte (80–99 %) | I 1 tilstand |
| FMR1fragile X messenger ribonucleoprotein 1 | Meget ofte (80–99 %) | I 1 tilstand |
| IGHMimmunoglobulin heavy constant mu | Meget ofte (80–99 %) | I 1 tilstand |
| IGLL1immunoglobulin lambda like polypeptide 1 | Meget ofte (80–99 %) | I 1 tilstand |
| LRRC8Aleucine rich repeat containing 8 VRAC subunit A | Meget ofte (80–99 %) | I 1 tilstand |
| PIK3CDphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | Meget ofte (80–99 %) | I 1 tilstand |
| PIK3R1phosphoinositide-3-kinase regulatory subunit 1 | Meget ofte (80–99 %) | I 1 tilstand |
| SPI1Spi-1 proto-oncogene | Meget ofte (80–99 %) | I 1 tilstand |
| TCF3transcription factor 3 | Meget ofte (80–99 %) | I 1 tilstand |
| WASWASP actin nucleation promoting factor | Meget ofte (80–99 %) | I 1 tilstand |
| APC2APC regulator of Wnt signaling pathway 2 | Ofte (30–79 %) | I 1 tilstand |
| ARVCFARVCF delta catenin family member | Ofte (30–79 %) | I 1 tilstand |
| BAZ1Bbromodomain adjacent to zinc finger domain 1B | Ofte (30–79 %) | I 1 tilstand |
| BRWD1bromodomain and WD repeat domain containing 1 | Ofte (30–79 %) | I 1 tilstand |
| BUD23BUD23 rRNA methyltransferase and ribosome maturation factor | Ofte (30–79 %) | I 1 tilstand |
| CCDC39coiled-coil domain 39 molecular ruler complex subunit | Ofte (30–79 %) | I 1 tilstand |
| CCDC40coiled-coil domain 40 molecular ruler complex subunit | Ofte (30–79 %) | I 1 tilstand |
| CCNOcyclin O | Ofte (30–79 %) | I 1 tilstand |
| CFAP221cilia and flagella associated protein 221 | Ofte (30–79 %) | I 1 tilstand |
| CFAP298cilia and flagella associated protein 298 | Ofte (30–79 %) | I 1 tilstand |
| CFAP300cilia and flagella associated protein 300 | Ofte (30–79 %) | I 2 tilstande |
| CFAP45cilia and flagella associated protein 45 | Ofte (30–79 %) | I 1 tilstand |
| CFAP74cilia and flagella associated protein 74 | Ofte (30–79 %) | I 1 tilstand |
| CLIP2CAP-Gly domain containing linker protein 2 | Ofte (30–79 %) | I 1 tilstand |
| CLXNcalaxin | Ofte (30–79 %) | I 1 tilstand |
| COMTcatechol-O-methyltransferase | Ofte (30–79 %) | I 1 tilstand |
| DAW1dynein assembly factor with WD repeats 1 | Ofte (30–79 %) | I 1 tilstand |
Vis 102 gener mere
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| DNAAF1dynein axonemal assembly factor 1 | Ofte (30–79 %) | I 1 tilstand |
| DNAAF11dynein axonemal assembly factor 11 | Ofte (30–79 %) | I 1 tilstand |
| DNAAF19dynein axonemal assembly factor 19 | Ofte (30–79 %) | I 1 tilstand |
| DNAAF3dynein axonemal assembly factor 3 | Ofte (30–79 %) | I 1 tilstand |
| DNAAF4dynein axonemal assembly factor 4 | Ofte (30–79 %) | I 1 tilstand |
| DNAAF5dynein axonemal assembly factor 5 | Ofte (30–79 %) | I 1 tilstand |
| DNAH1dynein axonemal heavy chain 1 | Ofte (30–79 %) | I 1 tilstand |
| DNAH11dynein axonemal heavy chain 11 | Ofte (30–79 %) | I 1 tilstand |
| DNAH5dynein axonemal heavy chain 5 | Ofte (30–79 %) | I 1 tilstand |
| DNAH7dynein axonemal heavy chain 7 | Ofte (30–79 %) | I 1 tilstand |
| DNAH9dynein axonemal heavy chain 9 | Ofte (30–79 %) | I 1 tilstand |
| DNAJB13DnaJ heat shock protein family (Hsp40) member B13 | Ofte (30–79 %) | I 1 tilstand |
| DNAJC30DnaJ heat shock protein family (Hsp40) member C30 | Ofte (30–79 %) | I 1 tilstand |
| DRC1dynein regulatory complex subunit 1 | Ofte (30–79 %) | I 1 tilstand |
| DRC2dynein regulatory complex subunit 2 | Ofte (30–79 %) | I 1 tilstand |
| DRC4dynein regulatory complex subunit 4 | Ofte (30–79 %) | I 1 tilstand |
| EIF4Heukaryotic translation initiation factor 4H | Ofte (30–79 %) | I 1 tilstand |
| ELNelastin | Ofte (30–79 %) | I 1 tilstand |
| FGFR2fibroblast growth factor receptor 2 | Ofte (30–79 %) | I 1 tilstand |
| FKBP6FKBP prolyl isomerase family member 6 (inactive) | Ofte (30–79 %) | I 1 tilstand |
| FOXJ1forkhead box J1 | Ofte (30–79 %) | I 1 tilstand |
| GAS2L2growth arrest specific 2 like 2 | Ofte (30–79 %) | I 1 tilstand |
| GATA2GATA binding protein 2 | Ofte (30–79 %) | I 1 tilstand |
| GP1BBglycoprotein Ib platelet subunit beta | Ofte (30–79 %) | I 1 tilstand |
| GTF2Igeneral transcription factor IIi | Ofte (30–79 %) | I 1 tilstand |
| GTF2IRD1GTF2I repeat domain containing 1 | Ofte (30–79 %) | I 1 tilstand |
| GTF2IRD2GTF2I repeat domain containing 2 | Ofte (30–79 %) | I 1 tilstand |
| HIRAhistone cell cycle regulator | Ofte (30–79 %) | I 1 tilstand |
| HYDINHYDIN axonemal central pair apparatus protein | Ofte (30–79 %) | I 1 tilstand |
| IL11RAinterleukin 11 receptor subunit alpha | Ofte (30–79 %) | I 1 tilstand |
| IRF6interferon regulatory factor 6 | Ofte (30–79 %) | I 1 tilstand |
| JMJD1Cjumonji domain containing 1C | Ofte (30–79 %) | I 1 tilstand |
| KDM6Alysine demethylase 6A | Ofte (30–79 %) | I 1 tilstand |
| KMT2Dlysine methyltransferase 2D | Ofte (30–79 %) | I 1 tilstand |
| LIMK1LIM domain kinase 1 | Ofte (30–79 %) | I 1 tilstand |
| LRRC56leucine rich repeat containing 56 | Ofte (30–79 %) | I 1 tilstand |
| MCIDASmulticiliate differentiation and DNA synthesis associated cell cycle protein | Ofte (30–79 %) | I 1 tilstand |
| METTL27methyltransferase like 27 | Ofte (30–79 %) | I 1 tilstand |
| MSX1msh homeobox 1 | Ofte (30–79 %) | I 1 tilstand |
| NCF1neutrophil cytosolic factor 1 | Ofte (30–79 %) | I 1 tilstand |
| NECTIN1nectin cell adhesion molecule 1 | Ofte (30–79 %) | I 1 tilstand |
| NEK10NIMA related kinase 10 | Ofte (30–79 %) | I 1 tilstand |
| NME5NME/NM23 family member 5 | Ofte (30–79 %) | I 1 tilstand |
| NME8NME/NM23 family member 8 | Ofte (30–79 %) | I 1 tilstand |
| NSD1nuclear receptor binding SET domain protein 1 | Ofte (30–79 %) | I 1 tilstand |
| NXNnucleoredoxin | Ofte (30–79 %) | I 1 tilstand |
| ODAD1outer dynein arm docking complex subunit 1 | Ofte (30–79 %) | I 1 tilstand |
| ODAD2outer dynein arm docking complex subunit 2 | Ofte (30–79 %) | I 1 tilstand |
| ODAD3outer dynein arm docking complex subunit 3 | Ofte (30–79 %) | I 1 tilstand |
| OFD1OFD1 centriole and centriolar satellite protein | Ofte (30–79 %) | I 2 tilstande |
| PGM3phosphoglucomutase 3 | Ofte (30–79 %) | I 1 tilstand |
| PIGHphosphatidylinositol glycan anchor biosynthesis class H | Ofte (30–79 %) | I 1 tilstand |
| RAI1retinoic acid induced 1 | Ofte (30–79 %) | I 1 tilstand |
| RFC2replication factor C subunit 2 | Ofte (30–79 %) | I 1 tilstand |
| ROR2ROR family WNT receptor 2 | Ofte (30–79 %) | I 1 tilstand |
| RPGRretinitis pigmentosa GTPase regulator | Ofte (30–79 %) | I 1 tilstand |
| RREB1ras responsive element binding protein 1 | Ofte (30–79 %) | I 1 tilstand |
| RSPH1radial spoke head component 1 | Ofte (30–79 %) | I 1 tilstand |
| RSPH3radial spoke head 3 | Ofte (30–79 %) | I 1 tilstand |
| RSPH4Aradial spoke head component 4A | Ofte (30–79 %) | I 1 tilstand |
| RSPH9radial spoke head component 9 | Ofte (30–79 %) | I 2 tilstande |
| RUNX2RUNX family transcription factor 2 | Ofte (30–79 %) | I 1 tilstand |
| SEC24CSEC24 homolog C, COPII component | Ofte (30–79 %) | I 1 tilstand |
| SHARPINSHANK associated RH domain interactor | Ofte (30–79 %) | I 1 tilstand |
| SLC25A12solute carrier family 25 member 12 | Ofte (30–79 %) | I 1 tilstand |
| SPAG1sperm associated antigen 1 | Ofte (30–79 %) | I 1 tilstand |
| SPEF2sperm flagellar and cilia associated 2 | Ofte (30–79 %) | I 1 tilstand |
| STAT3signal transducer and activator of transcription 3 | Ofte (30–79 %) | I 1 tilstand |
| STK36serine/threonine kinase 36 | Ofte (30–79 %) | I 1 tilstand |
| STX1Asyntaxin 1A | Ofte (30–79 %) | I 1 tilstand |
| TAF1TATA-box binding protein associated factor 1 | Ofte (30–79 %) | I 2 tilstande |
| TAF11TATA-box binding protein associated factor 11 | Ofte (30–79 %) | I 1 tilstand |
| TBL2transducin beta like 2 | Ofte (30–79 %) | I 1 tilstand |
| TBX1T-box transcription factor 1 | Ofte (30–79 %) | I 1 tilstand |
| TGDSTDP-glucose 4,6-dehydratase | Ofte (30–79 %) | I 1 tilstand |
| TMEM270transmembrane protein 270 | Ofte (30–79 %) | I 1 tilstand |
| TP63tumor protein p63 | Ofte (30–79 %) | I 1 tilstand |
| TTC12tetratricopeptide repeat domain 12 | Ofte (30–79 %) | I 1 tilstand |
| UFD1ubiquitin recognition factor in ER associated degradation 1 | Ofte (30–79 %) | I 1 tilstand |
| VPS37DVPS37D subunit of ESCRT-I | Ofte (30–79 %) | I 1 tilstand |
| ZMYND10zinc finger MYND-type containing 10 | Ofte (30–79 %) | I 1 tilstand |
| AGAaspartylglucosaminidase | Nogle gange (5–29 %) | I 1 tilstand |
| ANKRD11ankyrin repeat domain 11 | Nogle gange (5–29 %) | I 1 tilstand |
| CARMIL2capping protein regulator and myosin 1 linker 2 | Nogle gange (5–29 %) | I 1 tilstand |
| CPLX1complexin 1 | Nogle gange (5–29 %) | I 1 tilstand |
| CTBP1C-terminal binding protein 1 | Nogle gange (5–29 %) | I 1 tilstand |
| CTLA4cytotoxic T-lymphocyte associated protein 4 | Nogle gange (5–29 %) | I 1 tilstand |
| FOXN1forkhead box N1 | Nogle gange (5–29 %) | I 1 tilstand |
| GNB2G protein subunit beta 2 | Nogle gange (5–29 %) | I 1 tilstand |
| HLA-DPA1major histocompatibility complex, class II, DP alpha 1 | Nogle gange (5–29 %) | I 1 tilstand |
| HLA-DPB1major histocompatibility complex, class II, DP beta 1 | Nogle gange (5–29 %) | I 1 tilstand |
| KAT6Alysine acetyltransferase 6A | Nogle gange (5–29 %) | I 1 tilstand |
| LETM1leucine zipper and EF-hand containing transmembrane protein 1 | Nogle gange (5–29 %) | I 1 tilstand |
| NELFAnegative elongation factor complex member A | Nogle gange (5–29 %) | I 1 tilstand |
| NSD2nuclear receptor binding SET domain protein 2 | Nogle gange (5–29 %) | I 1 tilstand |
| OCRLOCRL inositol polyphosphate-5-phosphatase | Nogle gange (5–29 %) | I 1 tilstand |
| PIGGphosphatidylinositol glycan anchor biosynthesis class G (EMM blood group) | Nogle gange (5–29 %) | I 1 tilstand |
| PRTN3proteinase 3 | Nogle gange (5–29 %) | I 1 tilstand |
| PTPN22protein tyrosine phosphatase non-receptor type 22 | Nogle gange (5–29 %) | I 1 tilstand |
| TBX4T-box transcription factor 4 | Nogle gange (5–29 %) | I 1 tilstand |
| TAP1transporter 1, ATP binding cassette subfamily B member | Ikke registreret | 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 2026.10.19-9814e911.
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