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Normocytic anemia
A kind of anemia in which the volume of the red blood cells is normal.
Resumé
- Også kaldet
- Normocytic anaemia
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library(jsonlite)
url <- "https://dantelabs.com/traits/normocytic-anemia.json"
page <- fromJSON(url)
page$trait$nameLæs de gener, der er knyttet til Normocytic anemia, og resten af dit genom, med én test.
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Bestil min Genome Test22 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.
- Shwachman-Diamond SyndromeReads 2 of these genesEFL1SBDSAbout this report →
- Ghosal Haematodiaphyseal DysplasiaReads 1 of these genesTBXAS1About this report →
- Pyruvate Kinase Deficiency and Other Red Cell Enzyme DisordersReads 2 of these genesHK1TPI1About this report →
- Hereditary Gastrointestinal Stromal TumourReads 1 of these genesKITAbout this report →
Show 18 more reports
- Other Inborn Errors of ImmunityReads 6 of these genesATP6AP1ITPR3MYD88SBDSTET2TREX1About this report →
- Rare Inherited Bone Marrow Failure SyndromesReads 1 of these genesDNAJC21About this report →
- Systemic Lupus ErythematosusReads 1 of these genesTREX1About this report →
- Aicardi-Goutieres SyndromeReads 1 of these genesTREX1About this report →
- HyperinsulinismReads 1 of these genesHK1About this report →
- Type I InterferonopathiesReads 1 of these genesTREX1About this report →
- Diamond-Blackfan AnemiaReads 1 of these genesRPS29About this report →
- Charcot-Marie-Tooth DiseaseReads 2 of these genesITPR3HK1About this report →
- Homocystinuria & Cobalamin DisordersReads 1 of these genesMTRRAbout this report →
- Autoimmune DiseaseReads 1 of these genesTREX1About this report →
- Rare Monogenic Autoinflammatory DiseasesReads 1 of these genesTREX1About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesTOR1AAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 2 of these genesITPR3HK1About this report →
- Other Inherited LeukodystrophiesReads 1 of these genesTREX1About this report →
- Retinitis PigmentosaReads 1 of these genesHK1About this report →
- Congenital Disorders of GlycosylationReads 1 of these genesATP6AP1About this report →
- Intellectual DisabilityReads 1 of these genesASXL1About this report →
- Inherited Neurodegenerative DisordersReads 1 of these genesTREX1About this report →
Læs de gener, der er knyttet til Normocytic anemia, og resten af dit genom, med én test.
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Bestil min Genome Test19 gener knyttet til Normocytic anemia
Ændringer i disse gener forårsager sjældne tilstande, hvor Normocytic anemia 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 |
|---|---|---|
| ATP6AP1ATPase H+ transporting accessory protein 1 | Altid | I 1 tilstand |
| ITPR3inositol 1,4,5-trisphosphate receptor type 3 | Altid | I 1 tilstand |
| MTRR5-methyltetrahydrofolate-homocysteine methyltransferase reductase | Altid | I 1 tilstand |
| TBXAS1thromboxane A synthase 1 | Altid | I 1 tilstand |
| TOR1Atorsin family 1 member A | Altid | I 1 tilstand |
| EFL1elongation factor like GTPase 1 | Meget ofte (80–99 %) | I 2 tilstande |
| ASXL1ASXL transcriptional regulator 1 | Ofte (30–79 %) | I 1 tilstand |
| DNAJC21DnaJ heat shock protein family (Hsp40) member C21 | Ofte (30–79 %) | I 1 tilstand |
| KITKIT proto-oncogene, receptor tyrosine kinase | Ofte (30–79 %) | I 1 tilstand |
| MYD88MYD88 innate immune signal transduction adaptor | Ofte (30–79 %) | I 1 tilstand |
| SBDSSBDS ribosome maturation factor | Ofte (30–79 %) | I 1 tilstand |
| SF3B1splicing factor 3b subunit 1 | Ofte (30–79 %) | I 1 tilstand |
| SRSF2serine and arginine rich splicing factor 2 | Ofte (30–79 %) | I 1 tilstand |
| TET2tet methylcytosine dioxygenase 2 | Ofte (30–79 %) | I 3 tilstande |
| TREX1three prime repair exonuclease 1 | Ofte (30–79 %) | I 1 tilstand |
| ALDOAaldolase, fructose-bisphosphate A | Ikke registreret | I 1 tilstand |
| HK1hexokinase 1 | Ikke registreret | I 1 tilstand |
| RPS29ribosomal protein S29 | Ikke registreret | I 1 tilstand |
| TPI1triosephosphate isomerase 1 | 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 2026.10.21-777c9289.
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