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Tunnus
Hemolytic anemia
A type of anemia caused by premature destruction of red blood cells (hemolysis).
Kokkuvõte
- Teised nimetused
- Haemolytic anaemia, Haemolytic anemia, Hemolytic anaemia, Increased hemolysis
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Selle lehe andmed
Lehe aadressile saab lisada .json või päringusse application/json, et lugeda seda JSON-vormingus.
library(jsonlite)
url <- "https://dantelabs.com/traits/hemolytic-anemia.json"
page <- fromJSON(url)
page$trait$nameHemolytic anemiaHP:0001878
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Lugege välja geenid, mis on seotud Hemolytic anemia-ga, ja kogu ülejäänud genoom ühe testiga.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test62 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.
- Red Blood Cell Membrane DisordersReads 8 of these genesKCNN4RHAGRHCESLC4A1SPTBPIEZO1About this report →
- Hereditary SpherocytosisReads 5 of these genesANK1SLC4A1SPTBSPTA1EPB42About this report →
- PorphyriaReads 5 of these genesUROSURODALADCPOXFECHAbout this report →
- Aicardi-Goutieres SyndromeReads 4 of these genesADARIFIH1RNU7-1TREX1About this report →
Show 58 more reports
- Hepatic Porphyria DisordersReads 4 of these genesURODALADCPOXFECHAbout this report →
- Pyruvate Kinase Deficiency and Other Red Cell Enzyme DisordersReads 4 of these genesGCLCNT5C3AAK1TPI1About this report →
- Kabuki SyndromeReads 2 of these genesKDM6AKMT2DAbout this report →
- Other Inborn Errors of ImmunityReads 20 of these genesCYBC1IL2RACD46CFHCFIDEF6About this report →
- Hereditary Methaemoglobinaemia and Unstable HaemoglobinsReads 3 of these genesHBBHBA1HBA2About this report →
- ThalassaemiaReads 3 of these genesHBBHBA1HBA2About this report →
- Hemolytic Uremic Syndrome, Interstitial NephritisReads 4 of these genesCD46CFHCFIDGKEAbout this report →
- IPEX Syndrome and Other TregopathiesReads 3 of these genesIL2RADEF6CTLA4About this report →
- PolycythemiaReads 3 of these genesHBBHBA1HBA2About this report →
- Congenital Dyserythropoietic AnaemiasReads 2 of these genesCDAN1KLF1About this report →
- AlkaptonuriaReads 1 of these genesHGDAbout this report →
- COL4A1-Related DisorderReads 1 of these genesCOL4A1About this report →
- Dyschromatosis Symmetrica HereditariaReads 1 of these genesADARAbout this report →
- Glutathione Synthetase DeficiencyReads 1 of these genesGSSAbout this report →
- Rett Syndrome and MECP2-Related DisordersReads 1 of these genesMECP2About this report →
- Sickle Cell DiseaseReads 1 of these genesHBBAbout this report →
- Wilson DiseaseReads 1 of these genesATP7BAbout this report →
- Rare Monogenic Autoinflammatory DiseasesReads 5 of these genesADARIFIH1RNU7-1TNFAIP3TREX1About this report →
- Inherited Complement and Properdin DeficienciesReads 3 of these genesCFIC4AC4BAbout this report →
- Age-Related Macular DegenerationReads 1 of these genesCFHAbout this report →
- Hereditary Von Willebrand DiseaseReads 1 of these genesGP1BAAbout this report →
- Wiskott-Aldrich Syndrome SpectrumReads 1 of these genesWASAbout this report →
- Type I InterferonopathiesReads 2 of these genesIFIH1TREX1About this report →
- Disorder of Copper MetabolismReads 1 of these genesATP7BAbout this report →
- HyperlipidemiaReads 2 of these genesABCG5ABCG8About this report →
- GalactosemiaReads 1 of these genesGALTAbout this report →
- Hyper-IgM SyndromesReads 1 of these genesCD40LGAbout this report →
- Other Inherited LeukodystrophiesReads 4 of these genesADARIFIH1RNU7-1TREX1About this report →
- GPI Anchor Biosynthesis DefectsReads 2 of these genesPIGTPIGAAbout this report →
- Autoimmune DiseaseReads 2 of these genesCTLA4TREX1About this report →
- Chronic Granulomatous DiseaseReads 1 of these genesCYBC1About this report →
- Inflammatory Bowel Diseases (IBD)Reads 1 of these genesIL10About this report →
- Renal Tubular AcidosisReads 1 of these genesSLC4A1About this report →
- Systemic Lupus ErythematosusReads 1 of these genesTREX1About this report →
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 1 of these genesCTLA4About this report →
- Hereditary HypolipoproteinemiasReads 1 of these genesLCATAbout this report →
- Inherited ThrombocytopeniasReads 2 of these genesGATA1WASAbout this report →
- Inherited Platelet Function DisordersReads 1 of these genesGP1BAAbout this report →
- Common Variable Immunodeficiency (Monogenic CVID)Reads 1 of these genesCR2About this report →
- Congenital Disorders of GlycosylationReads 3 of these genesPIGTPIGAPGM3About this report →
- Severe Congenital NeutropeniaReads 1 of these genesWASAbout this report →
- Diamond-Blackfan AnemiaReads 1 of these genesGATA1About this report →
- Glycogen Storage DiseaseReads 1 of these genesPGK1About this report →
- Primary Lymphoedema & Lymphatic MalformationsReads 1 of these genesPIEZO1About this report →
- Neonatal Diabetes MellitusReads 1 of these genesIL2RAAbout this report →
- Epilepsy (Full Panel)Reads 3 of these genesSLC2A1PIGAMECP2About this report →
- Noonan SyndromeReads 1 of these genesNRASAbout this report →
- Syndromic Complex Neurodevelopmental DisorderReads 1 of these genesPAN2About this report →
- Inherited Neurodegenerative DisordersReads 4 of these genesADARIFIH1RNU7-1TREX1About this report →
- Nephrotic SyndromeReads 1 of these genesDGKEAbout this report →
- Diabetes MellitusReads 1 of these genesIL2RAAbout this report →
- Osteogenesis ImperfectaReads 1 of these genesIFIH1About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesSLC2A1About this report →
- DNA Repair DiseaseReads 1 of these genesNBNAbout this report →
- Female InfertilityReads 1 of these genesGALTAbout this report →
- Hypertrophic CardiomyopathyReads 1 of these genesNRASAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 1 of these genesCD59About this report →
- Intellectual DisabilityReads 1 of these genesMECP2About this report →
Lugege välja geenid, mis on seotud Hemolytic anemia-ga, ja kogu ülejäänud genoom ühe testiga.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test99 geeni on seotud tunnusega Hemolytic anemia
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Hemolytic anemia. Enamikul selle tunnusega inimestest ei ole ühtegi neist haigustest. Selles loendis olev geen ei ütle midagi kellegi enda genoomi kohta.
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| ANK1ankyrin 1 | Alati | Esineb 2 haiguses |
| ATP11CATPase phospholipid transporting 11C (ATP11C blood group) | Alati | Esineb 1 haiguses |
| CDAN1codanin 1 | Alati | Esineb 1 haiguses |
| CYBC1cytochrome b-245 chaperone 1 | Alati | Esineb 1 haiguses |
| GATA1GATA binding protein 1 | Alati | Esineb 3 haiguses |
| GCLCglutamate-cysteine ligase catalytic subunit | Alati | Esineb 2 haiguses |
| GSSglutathione synthetase | Alati | Esineb 2 haiguses |
| HMOX1heme oxygenase 1 | Alati | Esineb 2 haiguses |
| IL2RAinterleukin 2 receptor subunit alpha | Alati | Esineb 1 haiguses |
| KCNN4potassium calcium-activated channel subfamily N member 4 | Alati | Esineb 2 haiguses |
| KLF1KLF transcription factor 1 | Alati | Esineb 2 haiguses |
| NT5C3A5'-nucleotidase, cytosolic IIIA | Alati | Esineb 1 haiguses |
| PAN2poly(A) specific ribonuclease subunit PAN2 | Alati | Esineb 1 haiguses |
| PGK1phosphoglycerate kinase 1 | Alati | Esineb 2 haiguses |
| PIGTphosphatidylinositol glycan anchor biosynthesis class T | Alati | Esineb 1 haiguses |
| RHAGRh associated glycoprotein | Alati | Esineb 4 haiguses |
| RHCERh blood group CcEe antigens | Alati | Esineb 2 haiguses |
| SLC2A1solute carrier family 2 member 1 | Alati | Esineb 2 haiguses |
| SLC4A1solute carrier family 4 member 1 (Diego blood group) | Alati | Esineb 6 haiguses |
| SPTBspectrin beta, erythrocytic | Alati | Esineb 2 haiguses |
| CD46CD46 molecule | Väga sageli (80–99%) | Esineb 1 haiguses |
| CFHcomplement factor H | Väga sageli (80–99%) | Esineb 1 haiguses |
| CFIcomplement factor I | Väga sageli (80–99%) | Esineb 1 haiguses |
| HBBhemoglobin subunit beta | Väga sageli (80–99%) | Esineb 2 haiguses |
| HELLPARHELLP associated long non-coding RNA | Väga sageli (80–99%) | Esineb 1 haiguses |
| NBNnibrin | Väga sageli (80–99%) | Esineb 1 haiguses |
| PIEZO1piezo type mechanosensitive ion channel component 1 (Er blood group) | Väga sageli (80–99%) | Esineb 1 haiguses |
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Väga sageli (80–99%) | Esineb 1 haiguses |
| RHDRh blood group D antigen | Väga sageli (80–99%) | Esineb 1 haiguses |
| ABCG5ATP binding cassette subfamily G member 5 | Sageli (30–79%) | Esineb 1 haiguses |
| ABCG8ATP binding cassette subfamily G member 8 | Sageli (30–79%) | Esineb 1 haiguses |
| ALDOAaldolase, fructose-bisphosphate A | Sageli (30–79%) | Esineb 1 haiguses |
| ATP7BATPase copper transporting beta | Sageli (30–79%) | Esineb 2 haiguses |
| C1GALT1C1C1GALT1 specific chaperone 1 | Sageli (30–79%) | Esineb 1 haiguses |
| DEF6DEF6 guanine nucleotide exchange factor | Sageli (30–79%) | Esineb 1 haiguses |
| TPP2tripeptidyl peptidase 2 | Sageli (30–79%) | Esineb 1 haiguses |
| UROSuroporphyrinogen III synthase | Sageli (30–79%) | Esineb 2 haiguses |
| WASWASP actin nucleation promoting factor | Sageli (30–79%) | Esineb 1 haiguses |
| ADARadenosine deaminase RNA specific | Mõnikord (5–29%) | Esineb 1 haiguses |
| BANK1B cell scaffold protein with ankyrin repeats 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
Näita veel 59 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| BLKBLK proto-oncogene, Src family tyrosine kinase | Mõnikord (5–29%) | Esineb 1 haiguses |
| C4Acomplement C4A (Chido/Rodgers blood group) | Mõnikord (5–29%) | Esineb 1 haiguses |
| C4Bcomplement C4B (Chido/Rodgers blood group) | Mõnikord (5–29%) | Esineb 1 haiguses |
| CR2complement C3d receptor 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CTLA4cytotoxic T-lymphocyte associated protein 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DGKEdiacylglycerol kinase epsilon | Mõnikord (5–29%) | Esineb 1 haiguses |
| DNASE1deoxyribonuclease 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| EPB41erythrocyte membrane protein band 4.1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| ETS1ETS proto-oncogene 1, transcription factor | Mõnikord (5–29%) | Esineb 1 haiguses |
| FCGR2BFc gamma receptor IIb | Mõnikord (5–29%) | Esineb 2 haiguses |
| FCGR3BFc gamma receptor IIIb | Mõnikord (5–29%) | Esineb 1 haiguses |
| GNB2G protein subunit beta 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GYPCglycophorin C (Gerbich blood group) | Mõnikord (5–29%) | Esineb 1 haiguses |
| HGDhomogentisate 1,2-dioxygenase | Mõnikord (5–29%) | Esineb 1 haiguses |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| IFIH1interferon induced with helicase C domain 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| IGHG1immunoglobulin heavy constant gamma 1 (G1m marker) | Mõnikord (5–29%) | Esineb 1 haiguses |
| IL10interleukin 10 | Mõnikord (5–29%) | Esineb 1 haiguses |
| IRAK1interleukin 1 receptor associated kinase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| IRF5interferon regulatory factor 5 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ITGAMintegrin subunit alpha M | Mõnikord (5–29%) | Esineb 1 haiguses |
| JAZF1JAZF zinc finger 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| KIAA0319LKIAA0319 like | Mõnikord (5–29%) | Esineb 1 haiguses |
| MECP2methyl-CpG binding protein 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PDCD1programmed cell death 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PGM3phosphoglucomutase 3 | Mõnikord (5–29%) | Esineb 2 haiguses |
| PTPN22protein tyrosine phosphatase non-receptor type 22 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PXKPX domain containing serine/threonine kinase like | Mõnikord (5–29%) | Esineb 1 haiguses |
| RNU7-1RNA, U7 small nuclear 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SPP1secreted phosphoprotein 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SPTA1spectrin alpha, erythrocytic 1 | Mõnikord (5–29%) | Esineb 4 haiguses |
| STAT4signal transducer and activator of transcription 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TLR7toll like receptor 7 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TNFAIP3TNF alpha induced protein 3 | Mõnikord (5–29%) | Esineb 2 haiguses |
| TNFSF4TNF superfamily member 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TNIP1TNFAIP3 interacting protein 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TREX1three prime repair exonuclease 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| UBE2L3ubiquitin conjugating enzyme E2 L3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| URODuroporphyrinogen decarboxylase | Mõnikord (5–29%) | Esineb 1 haiguses |
| BTNL2butyrophilin like 2 | Harva (1–4%) | Esineb 1 haiguses |
| AK1adenylate kinase 1 | Pole registreeritud | Esineb 1 haiguses |
| ALADaminolevulinate dehydratase | Pole registreeritud | Esineb 1 haiguses |
| CD40LGCD40 ligand | Pole registreeritud | Esineb 1 haiguses |
| CD59CD59 molecule (CD59 blood group) | Pole registreeritud | Esineb 1 haiguses |
| COL4A1collagen type IV alpha 1 chain | Pole registreeritud | Esineb 1 haiguses |
| CPOXcoproporphyrinogen oxidase | Pole registreeritud | Esineb 1 haiguses |
| EPB42erythrocyte membrane protein band 4.2 | Pole registreeritud | Esineb 1 haiguses |
| FCGR2AFc gamma receptor IIa | Pole registreeritud | Esineb 1 haiguses |
| FECHferrochelatase | Pole registreeritud | Esineb 1 haiguses |
| GALTgalactose-1-phosphate uridylyltransferase | Pole registreeritud | Esineb 1 haiguses |
| GP1BAglycoprotein Ib platelet subunit alpha | Pole registreeritud | Esineb 1 haiguses |
| HBA1hemoglobin subunit alpha 1 | Pole registreeritud | Esineb 1 haiguses |
| HBA2hemoglobin subunit alpha 2 | Pole registreeritud | Esineb 1 haiguses |
| KDM6Alysine demethylase 6A | Pole registreeritud | Esineb 1 haiguses |
| KMT2Dlysine methyltransferase 2D | Pole registreeritud | Esineb 1 haiguses |
| LCATlecithin-cholesterol acyltransferase | Pole registreeritud | Esineb 1 haiguses |
| NRASNRAS proto-oncogene, GTPase | Pole registreeritud | Esineb 1 haiguses |
| PFKMphosphofructokinase, muscle | Pole registreeritud | Esineb 1 haiguses |
| TPI1triosephosphate isomerase 1 | Pole registreeritud | Esineb 1 haiguses |
Kui sageli see esineb geenist tulenevate seisunditega inimeste seas, kõige sagedamini nende kõigi seas, nagu on märgitud Inimese fenotüübi ontoloogias. Need lehed kirjeldavad tunnuseid ja nende taga olevaid uuringuid; need ei ole diagnoos ning sümptomite kohta tuleks küsida arstilt või geneetilt nõustajalt.
Kitsamad tunnused
- Autoimmune hemolytic anemia48 geeni
- Microangiopathic hemolytic anemia15 geeni
- Nonspherocytic hemolytic anemia11 geeni
- Coombs-positive hemolytic anemia10 geeni
- Congenital hemolytic anemia8 geeni
- Spontaneous hemolytic crises7 geeni
- Chronic hemolytic anemia5 geeni
- Episodic hemolytic anemia3 geeni
- Fava bean-induced hemolytic anemia3 geeni
- Heinz body anemia3 geeni
- Compensated hemolytic anemia1 geen
- Drug-sensitive hemolytic anemia1 geen
- Exercise-induced hemolysis1 geen
- Increased red cell hemolysis by shear stress1 geen
Laiemad tunnused
Allikas
- Inimese fenotüübi ontoloogia, versioon 2026-09-01: tunnus, selle nimetused, määratlus ja sellega seotud geenid. Lisateave leiab aadressilt hpo.jax.org.
- Andmeversioon 2026.10.19-9814e911.
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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.
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Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
