AtlasKenmerk
Decreased circulating complement C3 concentration
Concentration of the complement component C3 in the blood circulation below the lower limit of normal.
Samenvatting
- Ook bekend als
- Decreased serum C3, Decreased serum complement C3, Decreased serum complement C3 level
- Lichaamssysteem
- Abnormality of the immune system
AtlasDeze 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/decreased-circulating-complement-c3-concentration.json"
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page$trait$nameLees de genen die aan Decreased circulating complement C3 concentration gekoppeld zijn, en de rest van uw genoom, met één test.
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Mijn Genome Test bestellen21 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.
- Hemolytic Uremic Syndrome, Interstitial NephritisReads 6 of these genesC3CD46CFIDGKETHBDCFHAbout this report →
- Systemic Lupus ErythematosusReads 4 of these genesDNASE1L3SAT1PRKCDTREX1About this report →
- Autoimmune DiseaseReads 5 of these genesDNASE1L3SAT1CTLA4PRKCDTREX1About this report →
- Rett Syndrome and MECP2-Related DisordersReads 1 of these genesMECP2About this report →
Show 17 more reports
- Inherited Complement and Properdin DeficienciesReads 4 of these genesC3C4AC4BCFIAbout this report →
- Other Inborn Errors of ImmunityReads 14 of these genesC3SPINK5C4AC4BCD46CFIAbout this report →
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 2 of these genesCTLA4PRKCDAbout this report →
- Age-Related Macular DegenerationReads 1 of these genesCFHAbout this report →
- Inflammatory Bowel Diseases (IBD)Reads 1 of these genesIL10About this report →
- Hyper-IgE SyndromeReads 1 of these genesSPINK5About this report →
- IPEX Syndrome and Other TregopathiesReads 1 of these genesCTLA4About this report →
- Aicardi-Goutieres SyndromeReads 1 of these genesTREX1About this report →
- Rare Monogenic Autoinflammatory DiseasesReads 2 of these genesTNFAIP3TREX1About this report →
- ThrombophiliaReads 1 of these genesTHBDAbout this report →
- Common Variable Immunodeficiency (Monogenic CVID)Reads 1 of these genesCR2About this report →
- Type I InterferonopathiesReads 1 of these genesTREX1About this report →
- Nephrotic SyndromeReads 1 of these genesDGKEAbout this report →
- Epilepsy (Full Panel)Reads 2 of these genesLMNB2MECP2About this report →
- Intellectual DisabilityReads 2 of these genesMECP2PACS1About this report →
- Other Inherited LeukodystrophiesReads 1 of these genesTREX1About this report →
- Inherited Neurodegenerative DisordersReads 1 of these genesTREX1About this report →
Lees de genen die aan Decreased circulating complement C3 concentration gekoppeld zijn, en de rest van uw genoom, met één test.
Vanaf $ 449Gratis verzending · Resultaten binnen 6–8 weken
Mijn Genome Test bestellen45 genen gekoppeld aan Decreased circulating complement C3 concentration
Veranderingen in deze genen veroorzaken zeldzame aandoeningen waarbij Decreased circulating complement C3 concentration 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 |
|---|---|---|
| C3complement C3 | Altijd | In 2 aandoeningen |
| DNASE1L3deoxyribonuclease 1L3 | Altijd | In 1 aandoening |
| PLCG1phospholipase C gamma 1 | Altijd | In 1 aandoening |
| SPINK5serine peptidase inhibitor Kazal type 5 | Altijd | In 1 aandoening |
| IRAK1interleukin 1 receptor associated kinase 1 | Heel vaak (80–99%) | In 2 aandoeningen |
| SAT1spermidine/spermine N1-acetyltransferase 1 | Heel vaak (80–99%) | In 1 aandoening |
| SPP1secreted phosphoprotein 1 | Heel vaak (80–99%) | In 2 aandoeningen |
| STAT4signal transducer and activator of transcription 4 | Heel vaak (80–99%) | In 2 aandoeningen |
| 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 |
| C4Acomplement C4A (Chido/Rodgers blood group) | Vaak (30–79%) | In 1 aandoening |
| C4Bcomplement C4B (Chido/Rodgers blood group) | Vaak (30–79%) | In 1 aandoening |
| CD46CD46 molecule | Vaak (30–79%) | In 1 aandoening |
| CFIcomplement factor I | Vaak (30–79%) | In 2 aandoeningen |
| CR2complement C3d receptor 2 | Vaak (30–79%) | In 1 aandoening |
| CTLA4cytotoxic T-lymphocyte associated protein 4 | Vaak (30–79%) | In 1 aandoening |
| DGKEdiacylglycerol kinase epsilon | Vaak (30–79%) | In 1 aandoening |
| DNASE1deoxyribonuclease 1 | 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 1 aandoening |
| FCGR3BFc gamma receptor IIIb | Vaak (30–79%) | In 1 aandoening |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Vaak (30–79%) | In 1 aandoening |
| IGHG1immunoglobulin heavy constant gamma 1 (G1m marker) | Vaak (30–79%) | In 1 aandoening |
| IL10interleukin 10 | Vaak (30–79%) | In 1 aandoening |
| IRF5interferon regulatory factor 5 | Vaak (30–79%) | In 1 aandoening |
| 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 |
| LMNB2lamin B2 | Vaak (30–79%) | In 2 aandoeningen |
| MECP2methyl-CpG binding protein 2 | Vaak (30–79%) | In 1 aandoening |
| PDCD1programmed cell death 1 | Vaak (30–79%) | In 1 aandoening |
| PRKCDprotein kinase C delta | Vaak (30–79%) | In 1 aandoening |
| PTPN22protein tyrosine phosphatase non-receptor type 22 | Vaak (30–79%) | In 1 aandoening |
| PXKPX domain containing serine/threonine kinase like | Vaak (30–79%) | In 1 aandoening |
| THBDthrombomodulin | Vaak (30–79%) | In 1 aandoening |
| TLR7toll like receptor 7 | Vaak (30–79%) | In 2 aandoeningen |
| TNFAIP3TNF alpha induced protein 3 | 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 1 aandoening |
Toon nog 5 genen
| Gen | Hoe vaak het voorkomt | Aandoeningen |
|---|---|---|
| UBE2L3ubiquitin conjugating enzyme E2 L3 | Vaak (30–79%) | In 1 aandoening |
| PACS1phosphofurin acidic cluster sorting protein 1 | Soms (5–29%) | In 1 aandoening |
| CFHcomplement factor H | Niet vastgelegd | In 1 aandoening |
| CFHR1complement factor H related 1 | Niet vastgelegd | In 1 aandoening |
| CFHR3complement factor H related 3 | 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.
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.
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