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Kenmerk
Arthritis
Inflammation of a joint.
Samenvatting
- Ook bekend als
- Joint inflammation
- Lichaamssysteem
- Abnormality of the musculoskeletal system
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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/arthritis.json"
page <- fromJSON(url)
page$trait$nameArthritisHP:0001369
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Lees de genen die aan Arthritis gekoppeld zijn, en de rest van uw genoom, met één test.
Vanaf $ 449Gratis verzending · Resultaten binnen 6–8 weken
Mijn Genome Test bestellen84 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.
- Rare Monogenic Autoinflammatory DiseasesReads 17 of these genesELF4LYNPSTPIP1COPAPTPN2IL36RNAbout this report →
- Agammaglobulinaemia (XLA and Autosomal Forms)Reads 9 of these genesBLNKBTKCD79ACD79BIGHMIGLL1About this report →
- Aicardi-Goutieres SyndromeReads 8 of these genesTREX1ADARIFIH1RNASEH2ARNASEH2BRNASEH2CAbout this report →
- Other Inborn Errors of ImmunityReads 41 of these genesIKZF2C4ACD247FASIL10IL23RAbout this report →
Show 80 more reports
- Autoimmune DiseaseReads 10 of these genesFASNOD2CTLA4DNASE1L3PRKCDTREX1About this report →
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 5 of these genesFASCTLA4PRKCDCASP10FASLGAbout this report →
- IPEX Syndrome and Other TregopathiesReads 5 of these genesIL2RAIL2RBCTLA4FOXP3LRBAAbout this report →
- Hereditary Periodic Fever SyndromesReads 4 of these genesNLRP3MVKTNFRSF1ANLRP12About this report →
- Systemic Lupus ErythematosusReads 4 of these genesDNASE1L3PRKCDTREX1SAT1About this report →
- Activated PI3K-Delta Syndrome (APDS)Reads 2 of these genesPIK3CDPIK3R1About this report →
- Hereditary Multiple OsteochondromasReads 2 of these genesEXT1EXT2About this report →
- Inherited ArthropathiesReads 2 of these genesANKHPRG4About this report →
- HemochromatosisReads 3 of these genesHFEHJVTFR2About this report →
- Type I InterferonopathiesReads 4 of these genesCOPATREX1ACP5IFIH1About this report →
- 22q11.2 Deletion SyndromeReads 1 of these genesTBX1About this report →
- AlkaptonuriaReads 1 of these genesHGDAbout this report →
- Bent Bone Dysplasia Syndrome (FGFR2)Reads 1 of these genesFGFR2About this report →
- CLCN7-Related Hypopigmentation, Organomegaly and Delayed Myelination (HOD)Reads 1 of these genesCLCN7About this report →
- Deficiency of Adenosine Deaminase 2 (DADA2)Reads 1 of these genesADA2About this report →
- Dyschromatosis Symmetrica HereditariaReads 1 of these genesADARAbout this report →
- Fabry DiseaseReads 1 of these genesGLAAbout this report →
- Familial Mediterranean FeverReads 1 of these genesMEFVAbout this report →
- FGFR3-Related Chondrodysplasias (Achondroplasia and Related Conditions)Reads 1 of these genesFGFR3About this report →
- Nail-Patella SyndromeReads 1 of these genesLMX1BAbout this report →
- PIK3R1-Related DisordersReads 1 of these genesPIK3R1About this report →
- Rett Syndrome and MECP2-Related DisordersReads 1 of these genesMECP2About this report →
- Wilson DiseaseReads 1 of these genesATP7BAbout this report →
- Mendelian Susceptibility to Mycobacterial Disease (MSMD)Reads 3 of these genesIFNGR1IL23RIL12BAbout this report →
- Other Inherited LeukodystrophiesReads 8 of these genesTREX1ADARIFIH1RNASEH2ARNASEH2BRNASEH2CAbout this report →
- Inherited Complement and Properdin DeficienciesReads 3 of these genesC4AC1QBC4BAbout this report →
- Dent Disease and Lowe SyndromeReads 1 of these genesOCRLAbout this report →
- Familial Hidradenitis SuppurativaReads 1 of these genesPSENENAbout this report →
- Otospondylomegaepiphyseal Dysplasia (OSMED)Reads 1 of these genesCOL2A1About this report →
- Wiskott-Aldrich Syndrome SpectrumReads 1 of these genesWASAbout this report →
- Inherited Neurodegenerative DisordersReads 13 of these genesTBK1ASAH1TREX1ADARIFIH1RNASEH2AAbout this report →
- Common Variable Immunodeficiency (Monogenic CVID)Reads 2 of these genesCR2LRBAAbout this report →
- Disorder of Copper MetabolismReads 1 of these genesATP7BAbout this report →
- EBV-Driven Lymphoproliferation and CARD11 Immune DysregulationReads 1 of these genesIKZF2About this report →
- Neuroacanthocytosis and Huntington Disease PhenocopiesReads 1 of these genesVPS13AAbout this report →
- X-Linked Lymphoproliferative Disease and XMENReads 1 of these genesXIAPAbout this report →
- Severe Combined ImmunodeficiencyReads 3 of these genesCD247RAG1RAG2About this report →
- Hearing Loss and DeafnessReads 5 of these genesIKZF2PRPS1GJB2GJB6MYH14About this report →
- Achondrogenesis panelReads 1 of these genesCOL2A1About this report →
- Familial Paget Disease of BoneReads 1 of these genesTNFRSF11BAbout this report →
- Inherited Iron Metabolism DisordersReads 1 of these genesTFAbout this report →
- Moyamoya DiseaseReads 1 of these genesSAMHD1About this report →
- PorokeratosisReads 1 of these genesMVKAbout this report →
- Neonatal Diabetes MellitusReads 2 of these genesIL2RAHNF1BAbout this report →
- Autosomal Dominant Tubulointerstitial Kidney DiseaseReads 1 of these genesHNF1BAbout this report →
- Lynch SyndromeReads 1 of these genesEPCAMAbout this report →
- Syndromic CraniosynostosisReads 2 of these genesFGFR2FGFR3About this report →
- Heritable Pulmonary Arterial Hypertension (HPAH)Reads 1 of these genesCAV1About this report →
- Inflammatory Bowel Diseases (IBD)Reads 1 of these genesIL10About this report →
- Congenital Disorders of GlycosylationReads 4 of these genesEXT2KRT5POFUT1POGLUT1About this report →
- Lysosomal Storage DiseaseReads 3 of these genesASAH1GLAAGAAbout this report →
- Spinal Muscular AtrophyReads 2 of these genesASAH1UBA1About this report →
- Alpha-Mannosidosis and Other GlycoproteinosesReads 1 of these genesAGAAbout this report →
- Diabetes MellitusReads 2 of these genesIL2RAHNF1BAbout this report →
- Hereditary Rickets (Hypophosphatemic and Vitamin D-Dependent)Reads 1 of these genesPHEXAbout this report →
- Purine & Pyrimidine Metabolism DisordersReads 1 of these genesPRPS1About this report →
- Inherited ThrombocytopeniasReads 2 of these genesGP1BBWASAbout this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 2 of these genesGJB2GJB6About this report →
- Epiphyseal and Spondyloepiphyseal DysplasiasReads 1 of these genesCOL2A1About this report →
- Inherited Platelet Function DisordersReads 1 of these genesGP1BBAbout this report →
- LipodystrophyReads 1 of these genesCAV1About this report →
- Maturity-Onset Diabetes Of The YoungReads 1 of these genesHNF1BAbout this report →
- Severe Congenital NeutropeniaReads 1 of these genesWASAbout this report →
- Aortic AneurysmReads 1 of these genesTHSD4About this report →
- Congenital Diarrhoeas & EnteropathiesReads 1 of these genesEPCAMAbout this report →
- Frontotemporal DementiaReads 1 of these genesTBK1About this report →
- HyperlipidemiaReads 1 of these genesABCG8About this report →
- OsteopetrosisReads 1 of these genesCLCN7About this report →
- Ectodermal DysplasiasReads 1 of these genesGJB6About this report →
- Epidermolysis BullosaReads 1 of these genesKRT5About this report →
- VitreoretinopathyReads 1 of these genesCOL2A1About this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 1 of these genesTBK1About this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesPOGLUT1About this report →
- Osteogenesis ImperfectaReads 1 of these genesIFIH1About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesRNF168About this report →
- Rare Hereditary Peripheral NeuropathiesReads 2 of these genesPRPS1VPS13AAbout this report →
- Intellectual DisabilityReads 2 of these genesMECP2JMJD1CAbout this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesPRPS1About this report →
- Primary Mitochondrial DiseaseReads 1 of these genesC2orf69About this report →
- Epilepsy (Full Panel)Reads 1 of these genesMECP2About this report →
Lees de genen die aan Arthritis gekoppeld zijn, en de rest van uw genoom, met één test.
Vanaf $ 449Gratis verzending · Resultaten binnen 6–8 weken
Mijn Genome Test bestellen173 genen gekoppeld aan Arthritis
Veranderingen in deze genen veroorzaken zeldzame aandoeningen waarbij Arthritis 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 |
|---|---|---|
| ELF4E74 like ETS transcription factor 4 | Altijd | In 1 aandoening |
| IKZF2IKAROS family zinc finger 2 | Altijd | In 1 aandoening |
| LYNLYN proto-oncogene, Src family tyrosine kinase | Altijd | In 1 aandoening |
| NLRP3NLR family pyrin domain containing 3 | Altijd | In 5 aandoeningen |
| PDCD1programmed cell death 1 | Altijd | In 2 aandoeningen |
| PLD4phospholipase D family member 4 | Altijd | In 1 aandoening |
| PSTPIP1proline-serine-threonine phosphatase interacting protein 1 | Altijd | In 2 aandoeningen |
| TBK1TANK binding kinase 1 | Altijd | In 1 aandoening |
| TRAF3TNF receptor associated factor 3 | Altijd | In 1 aandoening |
| ANKHANKH inorganic pyrophosphate transport regulator | Heel vaak (80–99%) | In 1 aandoening |
| ANKRD55ankyrin repeat domain 55 | Heel vaak (80–99%) | In 2 aandoeningen |
| ASAH1N-acylsphingosine amidohydrolase 1 | Heel vaak (80–99%) | In 2 aandoeningen |
| ATP7BATPase copper transporting beta | Heel vaak (80–99%) | In 1 aandoening |
| C4Acomplement C4A (Chido/Rodgers blood group) | Heel vaak (80–99%) | In 2 aandoeningen |
| CCR1C-C motif chemokine receptor 1 | Heel vaak (80–99%) | In 1 aandoening |
| CD247CD247 molecule | Heel vaak (80–99%) | In 2 aandoeningen |
| CD4CD4 molecule | Heel vaak (80–99%) | In 1 aandoening |
| CLCN7Cl-/H+ antiporter 7 | Heel vaak (80–99%) | In 1 aandoening |
| COPAcoat protein complex I subunit alpha | Heel vaak (80–99%) | In 1 aandoening |
| ERAP1endoplasmic reticulum aminopeptidase 1 | Heel vaak (80–99%) | In 1 aandoening |
| FASFas cell surface death receptor | Heel vaak (80–99%) | In 2 aandoeningen |
| GLAgalactosidase alpha | Heel vaak (80–99%) | In 1 aandoening |
| HGDhomogentisate 1,2-dioxygenase | Heel vaak (80–99%) | In 2 aandoeningen |
| HLA-Bmajor histocompatibility complex, class I, B | Heel vaak (80–99%) | In 4 aandoeningen |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Heel vaak (80–99%) | In 6 aandoeningen |
| IFNGR1interferon gamma receptor 1 | Heel vaak (80–99%) | In 1 aandoening |
| IL10interleukin 10 | Heel vaak (80–99%) | In 2 aandoeningen |
| IL12Ainterleukin 12A | Heel vaak (80–99%) | In 1 aandoening |
| IL12A-AS1IL12A antisense RNA 1 | Heel vaak (80–99%) | In 1 aandoening |
| IL23Rinterleukin 23 receptor | Heel vaak (80–99%) | In 1 aandoening |
| IL2RAinterleukin 2 receptor subunit alpha | Heel vaak (80–99%) | In 2 aandoeningen |
| IL2RBinterleukin 2 receptor subunit beta | Heel vaak (80–99%) | In 2 aandoeningen |
| IL6interleukin 6 | Heel vaak (80–99%) | In 1 aandoening |
| IRF4interferon regulatory factor 4 | Heel vaak (80–99%) | In 2 aandoeningen |
| KLRC4killer cell lectin like receptor C4 | Heel vaak (80–99%) | In 1 aandoening |
| LACC1laccase domain multifunctional purine nucleosidase 1 | Heel vaak (80–99%) | In 1 aandoening |
| MEFVMEFV innate immunity regulator, pyrin | Heel vaak (80–99%) | In 3 aandoeningen |
| MIFmacrophage migration inhibitory factor | Heel vaak (80–99%) | In 1 aandoening |
| MMP14matrix metallopeptidase 14 | Heel vaak (80–99%) | In 1 aandoening |
| MMP2matrix metallopeptidase 2 | Heel vaak (80–99%) | In 1 aandoening |
Toon nog 133 genen
| Gen | Hoe vaak het voorkomt | Aandoeningen |
|---|---|---|
| NOD2nucleotide binding oligomerization domain containing 2 | Heel vaak (80–99%) | In 3 aandoeningen |
| PTPN2protein tyrosine phosphatase non-receptor type 2 | Heel vaak (80–99%) | In 2 aandoeningen |
| PTPN22protein tyrosine phosphatase non-receptor type 22 | Heel vaak (80–99%) | In 5 aandoeningen |
| STAT4signal transducer and activator of transcription 4 | Heel vaak (80–99%) | In 5 aandoeningen |
| TLR4toll like receptor 4 | Heel vaak (80–99%) | In 1 aandoening |
| TNFRSF11BTNF receptor superfamily member 11b | Heel vaak (80–99%) | In 1 aandoening |
| UBAC2UBA domain containing 2 | Heel vaak (80–99%) | In 1 aandoening |
| AP1S3adaptor related protein complex 1 subunit sigma 3 | Vaak (30–79%) | In 1 aandoening |
| BANK1B cell scaffold protein with ankyrin repeats 1 | Vaak (30–79%) | In 1 aandoening |
| BLKBLK proto-oncogene, Src family tyrosine kinase | Vaak (30–79%) | In 1 aandoening |
| BLNKB cell linker | Vaak (30–79%) | In 1 aandoening |
| BTKBruton tyrosine kinase | Vaak (30–79%) | In 1 aandoening |
| C1QBcomplement C1q B chain | Vaak (30–79%) | In 1 aandoening |
| C2orf69chromosome 2 open reading frame 69 | Vaak (30–79%) | In 1 aandoening |
| C4Bcomplement C4B (Chido/Rodgers blood group) | Vaak (30–79%) | In 1 aandoening |
| CAV1caveolin 1 | Vaak (30–79%) | In 1 aandoening |
| CCN2cellular communication network factor 2 | Vaak (30–79%) | In 1 aandoening |
| CCR6C-C motif chemokine receptor 6 | Vaak (30–79%) | In 1 aandoening |
| CD79ACD79a molecule | Vaak (30–79%) | In 1 aandoening |
| CD79BCD79b molecule | Vaak (30–79%) | In 1 aandoening |
| COL2A1collagen type II alpha 1 chain | Vaak (30–79%) | In 1 aandoening |
| CR2complement C3d receptor 2 | Vaak (30–79%) | In 1 aandoening |
| CTLA4cytotoxic T-lymphocyte associated protein 4 | Vaak (30–79%) | In 3 aandoeningen |
| DNASE1deoxyribonuclease 1 | Vaak (30–79%) | In 2 aandoeningen |
| DNASE1L3deoxyribonuclease 1L3 | Vaak (30–79%) | In 1 aandoening |
| ETS1ETS proto-oncogene 1, transcription factor | Vaak (30–79%) | In 1 aandoening |
| FCGR2BFc gamma receptor IIb | Vaak (30–79%) | In 2 aandoeningen |
| FCGR3BFc gamma receptor IIIb | Vaak (30–79%) | In 1 aandoening |
| HLA-DPA1major histocompatibility complex, class II, DP alpha 1 | Vaak (30–79%) | In 1 aandoening |
| HLA-DPB1major histocompatibility complex, class II, DP beta 1 | Vaak (30–79%) | In 1 aandoening |
| HPGD15-hydroxyprostaglandin dehydrogenase | Vaak (30–79%) | In 3 aandoeningen |
| IGHG1immunoglobulin heavy constant gamma 1 (G1m marker) | Vaak (30–79%) | In 1 aandoening |
| IGHMimmunoglobulin heavy constant mu | Vaak (30–79%) | In 1 aandoening |
| IGLL1immunoglobulin lambda like polypeptide 1 | Vaak (30–79%) | In 1 aandoening |
| IL12Binterleukin 12B | Vaak (30–79%) | In 1 aandoening |
| IL36RNinterleukin 36 receptor antagonist | Vaak (30–79%) | In 1 aandoening |
| IRAK1interleukin 1 receptor associated kinase 1 | Vaak (30–79%) | In 2 aandoeningen |
| IRF5interferon regulatory factor 5 | Vaak (30–79%) | In 2 aandoeningen |
| ITGAMintegrin subunit alpha M | Vaak (30–79%) | In 1 aandoening |
| JAZF1JAZF zinc finger 1 | Vaak (30–79%) | In 1 aandoening |
| KIAA0319LKIAA0319 like | Vaak (30–79%) | In 1 aandoening |
| KNSTRNkinetochore localized astrin (SPAG5) binding protein | Vaak (30–79%) | In 2 aandoeningen |
| LBRlamin B receptor | Vaak (30–79%) | In 1 aandoening |
| LMX1BLIM homeobox transcription factor 1 beta | Vaak (30–79%) | In 1 aandoening |
| LRRC8Aleucine rich repeat containing 8 VRAC subunit A | Vaak (30–79%) | In 1 aandoening |
| MECP2methyl-CpG binding protein 2 | Vaak (30–79%) | In 1 aandoening |
| MLXMAX dimerization protein MLX | Vaak (30–79%) | In 1 aandoening |
| MVKmevalonate kinase | Vaak (30–79%) | In 2 aandoeningen |
| OCRLOCRL inositol polyphosphate-5-phosphatase | Vaak (30–79%) | In 1 aandoening |
| P4HA2prolyl 4-hydroxylase subunit alpha 2 | Vaak (30–79%) | In 1 aandoening |
| PIK3CDphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | Vaak (30–79%) | In 3 aandoeningen |
| PIK3R1phosphoinositide-3-kinase regulatory subunit 1 | Vaak (30–79%) | In 1 aandoening |
| PRKCDprotein kinase C delta | Vaak (30–79%) | In 1 aandoening |
| PRPS1phosphoribosyl pyrophosphate synthetase 1 | Vaak (30–79%) | In 2 aandoeningen |
| PRTN3proteinase 3 | Vaak (30–79%) | In 1 aandoening |
| PXKPX domain containing serine/threonine kinase like | Vaak (30–79%) | In 1 aandoening |
| SHARPINSHANK associated RH domain interactor | Vaak (30–79%) | In 1 aandoening |
| SLCO2A1solute carrier organic anion transporter family member 2A1 | Vaak (30–79%) | In 1 aandoening |
| SPI1Spi-1 proto-oncogene | Vaak (30–79%) | In 1 aandoening |
| SPP1secreted phosphoprotein 1 | Vaak (30–79%) | In 2 aandoeningen |
| TCF3transcription factor 3 | Vaak (30–79%) | In 1 aandoening |
| TLR7toll like receptor 7 | Vaak (30–79%) | In 1 aandoening |
| TNFAIP3TNF alpha induced protein 3 | Vaak (30–79%) | In 1 aandoening |
| TNFRSF1ATNF receptor superfamily member 1A | Vaak (30–79%) | In 1 aandoening |
| TNFSF4TNF superfamily member 4 | Vaak (30–79%) | In 1 aandoening |
| TNIP1TNFAIP3 interacting protein 1 | Vaak (30–79%) | In 1 aandoening |
| TREX1three prime repair exonuclease 1 | Vaak (30–79%) | In 3 aandoeningen |
| UBE2L3ubiquitin conjugating enzyme E2 L3 | Vaak (30–79%) | In 1 aandoening |
| ACP5acid phosphatase 5, tartrate resistant | Soms (5–29%) | In 1 aandoening |
| ADARadenosine deaminase RNA specific | Soms (5–29%) | In 1 aandoening |
| AGAaspartylglucosaminidase | Soms (5–29%) | In 1 aandoening |
| ARVCFARVCF delta catenin family member | Soms (5–29%) | In 1 aandoening |
| BMP6bone morphogenetic protein 6 | Soms (5–29%) | In 1 aandoening |
| BTNL2butyrophilin like 2 | Soms (5–29%) | In 1 aandoening |
| COMTcatechol-O-methyltransferase | Soms (5–29%) | In 1 aandoening |
| EPCAMepithelial cell adhesion molecule | Soms (5–29%) | In 2 aandoeningen |
| EXT1exostosin glycosyltransferase 1 | Soms (5–29%) | In 1 aandoening |
| EXT2exostosin glycosyltransferase 2 | Soms (5–29%) | In 1 aandoening |
| FOXP3forkhead box P3 | Soms (5–29%) | In 1 aandoening |
| GJB2gap junction protein beta 2 | Soms (5–29%) | In 1 aandoening |
| GJB6gap junction protein beta 6 | Soms (5–29%) | In 1 aandoening |
| GP1BBglycoprotein Ib platelet subunit beta | Soms (5–29%) | In 1 aandoening |
| HFEhomeostatic iron regulator | Soms (5–29%) | In 1 aandoening |
| HIRAhistone cell cycle regulator | Soms (5–29%) | In 1 aandoening |
| HNF1BHNF1 homeobox B | Soms (5–29%) | In 1 aandoening |
| IFIH1interferon induced with helicase C domain 1 | Soms (5–29%) | In 2 aandoeningen |
| IGHG2immunoglobulin heavy constant gamma 2 (G2m marker) | Soms (5–29%) | In 1 aandoening |
| IGKCimmunoglobulin kappa constant | Soms (5–29%) | In 1 aandoening |
| JMJD1Cjumonji domain containing 1C | Soms (5–29%) | In 1 aandoening |
| LRBALPS responsive beige-like anchor protein | Soms (5–29%) | In 1 aandoening |
| LSM11LSM11, U7 small nuclear RNA associated | Soms (5–29%) | In 1 aandoening |
| PHEXphosphate regulating endopeptidase X-linked | Soms (5–29%) | In 1 aandoening |
| RNASEH2Aribonuclease H2 subunit A | Soms (5–29%) | In 1 aandoening |
| RNASEH2Bribonuclease H2 subunit B | Soms (5–29%) | In 1 aandoening |
| RNASEH2Cribonuclease H2 subunit C | Soms (5–29%) | In 1 aandoening |
| RNF168ring finger protein 168 | Soms (5–29%) | In 1 aandoening |
| RNU7-1RNA, U7 small nuclear 1 | Soms (5–29%) | In 1 aandoening |
| RREB1ras responsive element binding protein 1 | Soms (5–29%) | In 1 aandoening |
| SAMHD1SAM and HD domain containing deoxynucleoside triphosphate triphosphohydrolase 1 | Soms (5–29%) | In 1 aandoening |
| SAT1spermidine/spermine N1-acetyltransferase 1 | Soms (5–29%) | In 1 aandoening |
| SEC24CSEC24 homolog C, COPII component | Soms (5–29%) | In 1 aandoening |
| SYKspleen associated tyrosine kinase | Soms (5–29%) | In 1 aandoening |
| TBX1T-box transcription factor 1 | Soms (5–29%) | In 1 aandoening |
| TFtransferrin | Soms (5–29%) | In 1 aandoening |
| THSD4thrombospondin type 1 domain containing 4 | Soms (5–29%) | In 1 aandoening |
| UFD1ubiquitin recognition factor in ER associated degradation 1 | Soms (5–29%) | In 1 aandoening |
| VPS13Avacuolar protein sorting 13 homolog A | Soms (5–29%) | In 1 aandoening |
| WASWASP actin nucleation promoting factor | Soms (5–29%) | In 1 aandoening |
| XIAPX-linked inhibitor of apoptosis | Soms (5–29%) | In 1 aandoening |
| CASP10caspase 10 | Zelden (1–4%) | In 1 aandoening |
| FASLGFas ligand | Zelden (1–4%) | In 1 aandoening |
| FGF10fibroblast growth factor 10 | Zelden (1–4%) | In 1 aandoening |
| FGFR2fibroblast growth factor receptor 2 | Zelden (1–4%) | In 1 aandoening |
| FGFR3fibroblast growth factor receptor 3 | Zelden (1–4%) | In 1 aandoening |
| KRT5keratin 5 | Zelden (1–4%) | In 1 aandoening |
| MYH14myosin heavy chain 14 | Zelden (1–4%) | In 1 aandoening |
| POFUT1protein O-fucosyltransferase 1 | Zelden (1–4%) | In 1 aandoening |
| POGLUT1protein O-glucosyltransferase 1 | Zelden (1–4%) | In 1 aandoening |
| PSENENpresenilin enhancer, gamma-secretase subunit | Zelden (1–4%) | In 1 aandoening |
| ABCG2ATP binding cassette subfamily G member 2 (JR blood group) | Niet vastgelegd | In 1 aandoening |
| ABCG8ATP binding cassette subfamily G member 8 | Niet vastgelegd | In 1 aandoening |
| ADA2adenosine deaminase 2 | Niet vastgelegd | In 1 aandoening |
| FCGR2AFc gamma receptor IIa | Niet vastgelegd | In 1 aandoening |
| HJVhemojuvelin BMP co-receptor | Niet vastgelegd | In 1 aandoening |
| HLA-Cmajor histocompatibility complex, class I, C | Niet vastgelegd | In 1 aandoening |
| HOXD10homeobox D10 | Niet vastgelegd | In 1 aandoening |
| NLRP12NLR family pyrin domain containing 12 | Niet vastgelegd | In 1 aandoening |
| PRG4proteoglycan 4 | Niet vastgelegd | In 1 aandoening |
| PSMB4proteasome 20S subunit beta 4 | Niet vastgelegd | In 1 aandoening |
| RAG1recombination activating 1 | Niet vastgelegd | In 1 aandoening |
| RAG2recombination activating 2 | Niet vastgelegd | In 1 aandoening |
| TFR2transferrin receptor 2 | Niet vastgelegd | In 1 aandoening |
| UBA1ubiquitin like modifier activating enzyme 1 | 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 2026.10.18-8b139e39.
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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.
Vanaf $ 449
Gratis verzending · Resultaten binnen 6–8 weken
