AtlasEgenskap
Microcytic anemia
A kind of anemia in which the volume of the red blood cells is reduced.
Sammanfattning
- Även kallad
- Microcytic anaemia
- Kroppssystem
- Abnormality of blood and blood-forming tissues
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library(jsonlite)
url <- "https://dantelabs.com/traits/microcytic-anemia.json"
page <- fromJSON(url)
page$trait$nameLäs generna kopplade till Microcytic anemia, och resten av ditt genom, med ett enda test.
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Beställ mitt Genome Test31 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.
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- Acid Sphingomyelinase Deficiency (Niemann-Pick Disease Types A and B)Reads 1 of these genesSMPD1About this report →
Show 27 more reports
- H SyndromeReads 1 of these genesSLC29A3About this report →
- Sickle Cell DiseaseReads 1 of these genesHBBAbout this report →
- Wiskott-Aldrich Syndrome SpectrumReads 1 of these genesWASAbout this report →
- Leukocyte Adhesion DeficiencyReads 1 of these genesSLC35C1About this report →
- Rare Monogenic Autoinflammatory DiseasesReads 3 of these genesPSTPIP1LPIN2PSMB8About this report →
- Hereditary Vascular MalformationsReads 1 of these genesTEKAbout this report →
- MTOR Pathway Megalencephaly and Overgrowth DisordersReads 1 of these genesPIK3CAAbout this report →
- Hyper-IgE SyndromeReads 1 of these genesIL6STAbout this report →
- GlaucomaReads 1 of these genesTEKAbout this report →
- Hepatic Porphyria DisordersReads 1 of these genesFECHAbout this report →
- Hereditary Sideroblastic AnaemiasReads 1 of these genesPUS1About this report →
- PorphyriaReads 1 of these genesFECHAbout this report →
- Congenital Disorders of GlycosylationReads 3 of these genesSLC37A4SLC35C1SRD5A3About this report →
- Severe Congenital NeutropeniaReads 1 of these genesWASAbout this report →
- Type I InterferonopathiesReads 1 of these genesPSMB8About this report →
- Frontotemporal DementiaReads 1 of these genesTBK1About this report →
- Glycogen Storage DiseaseReads 1 of these genesSLC37A4About this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 1 of these genesATRXAbout this report →
- Other Inborn Errors of ImmunityReads 3 of these genesIL6STRIPK1WASAbout this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 1 of these genesTBK1About this report →
- Inherited ThrombocytopeniasReads 1 of these genesWASAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 2 of these genesSUCLA2SMPD1About this report →
- Lysosomal Storage DiseaseReads 1 of these genesSMPD1About this report →
- Leigh SyndromeReads 1 of these genesSUCLA2About this report →
- Inherited Neurodegenerative DisordersReads 2 of these genesIREB2TBK1About this report →
- Primary Mitochondrial DiseaseReads 1 of these genesSUCLA2About this report →
- Intellectual DisabilityReads 1 of these genesATRXAbout this report →
Läs generna kopplade till Microcytic anemia, och resten av ditt genom, med ett enda test.
Från 449 $Fri frakt · Resultat inom 6–8 veckor
Beställ mitt Genome Test32 gener kopplade till Microcytic anemia
Förändringar i dessa gener orsakar sällsynta tillstånd där Microcytic anemia förekommer. De flesta med denna egenskap har inget av dessa tillstånd, och en gen på listan säger ingenting om någons eget genom.
| Gen | Hur ofta den förekommer | Tillstånd |
|---|---|---|
| FARSAphenylalanyl-tRNA synthetase subunit alpha | Alltid | I 1 tillstånd |
| HBBhemoglobin subunit beta | Alltid | I 4 tillstånd |
| IL6STinterleukin 6 cytokine family signal transducer | Alltid | I 1 tillstånd |
| IREB2iron responsive element binding protein 2 | Alltid | I 1 tillstånd |
| IRX5iroquois homeobox 5 | Alltid | I 1 tillstånd |
| PSTPIP1proline-serine-threonine phosphatase interacting protein 1 | Alltid | I 1 tillstånd |
| RIPK1receptor interacting serine/threonine kinase 1 | Alltid | I 1 tillstånd |
| SLC25A10solute carrier family 25 member 10 | Alltid | I 1 tillstånd |
| SLC25A21solute carrier family 25 member 21 | Alltid | I 1 tillstånd |
| SLC37A4solute carrier family 37 member 4 | Alltid | I 1 tillstånd |
| SUCLA2succinate-CoA ligase ADP-forming subunit beta | Alltid | I 1 tillstånd |
| ATRXATRX chromatin remodeler | Mycket ofta (80–99 %) | I 1 tillstånd |
| HBA1hemoglobin subunit alpha 1 | Mycket ofta (80–99 %) | I 1 tillstånd |
| HBA2hemoglobin subunit alpha 2 | Mycket ofta (80–99 %) | I 1 tillstånd |
| HBDhemoglobin subunit delta | Mycket ofta (80–99 %) | I 1 tillstånd |
| HBG1hemoglobin subunit gamma 1 | Mycket ofta (80–99 %) | I 1 tillstånd |
| LPIN2lipin 2 | Ofta (30–79 %) | I 1 tillstånd |
| SLC35C1solute carrier family 35 member C1 | Ofta (30–79 %) | I 1 tillstånd |
| SRD5A3steroid 5 alpha-reductase 3 | Ofta (30–79 %) | I 2 tillstånd |
| TBK1TANK binding kinase 1 | Ofta (30–79 %) | I 1 tillstånd |
| WASWASP actin nucleation promoting factor | Ofta (30–79 %) | I 1 tillstånd |
| AGGF1angiogenic factor with G-patch and FHA domains 1 | Ibland (5–29 %) | I 1 tillstånd |
| CATcatalase | Ibland (5–29 %) | I 1 tillstånd |
| FECHferrochelatase | Ibland (5–29 %) | I 1 tillstånd |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Ibland (5–29 %) | I 1 tillstånd |
| PSMB8proteasome 20S subunit beta 8 | Ibland (5–29 %) | I 1 tillstånd |
| SLC29A3solute carrier family 29 member 3 | Ibland (5–29 %) | I 1 tillstånd |
| TEKTEK receptor tyrosine kinase | Ibland (5–29 %) | I 1 tillstånd |
| FDX2ferredoxin 2 | Sällan (1–4%) | I 1 tillstånd |
| PUS1pseudouridine synthase 1 | Inte registrerat | I 1 tillstånd |
| SMPD1sphingomyelin phosphodiesterase 1 | Inte registrerat | I 1 tillstånd |
| TKFCtriokinase and FMN cyclase | Inte registrerat | I 1 tillstånd |
Hur ofta det förekommer hos personer med ett av genens tillstånd, den vanligaste frekvensen bland dem, enligt Human Phenotype Ontology. Dessa sidor beskriver egenskaper och forskningen bakom dem. De är inte en diagnos, och det är läkare eller genetisk rådgivare du bör fråga om symtom.
Mer specifika egenskaper
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Varifrån informationen kommer
- Human Phenotype Ontology, version 2026-09-01: egenskapen, dess namn, definition och de gener som är kopplade till den. Läs mer på hpo.jax.org.
- Dataversion 2026.10.21-777c9289.
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