AtlasTræk
Anemic pallor
A type of pallor that is secondary to the presence of anemia.
Resumé
- Også kaldet
- Anaemic pallor
- Kropssystem
- Abnormality of the integument
AtlasDenne side som data
Tilføj .json til sidens adresse, eller bed om application/json, for at læse den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/anemic-pallor.json"
page <- fromJSON(url)
page$trait$nameLæs de gener, der er knyttet til Anemic pallor, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test20 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.
- Juvenile Polyposis SyndromeReads 2 of these genesBMPR1ASMAD4About this report →
- Neuroblastoma Predisposition (ALK and PHOX2B)Reads 2 of these genesALKPHOX2BAbout this report →
- Hereditary Hemorrhagic TelangiectasiaReads 2 of these genesENGSMAD4About this report →
- Congenital Central Hypoventilation SyndromeReads 1 of these genesPHOX2BAbout this report →
Show 16 more reports
- Feingold Syndrome Type 1Reads 1 of these genesMYCNAbout this report →
- Fanconi AnemiaReads 4 of these genesFANCAFANCCFANCD2FANCEAbout this report →
- Hereditary Mixed Polyposis SyndromeReads 1 of these genesBMPR1AAbout this report →
- DNA Repair DiseaseReads 4 of these genesFANCAFANCCFANCD2FANCEAbout this report →
- Hirschsprung Disease & Related Enteric NeurocristopathiesReads 1 of these genesPHOX2BAbout this report →
- Inherited Iron Metabolism DisordersReads 1 of these genesTMPRSS6About this report →
- Hereditary SpherocytosisReads 1 of these genesSLC4A1About this report →
- Renal Tubular AcidosisReads 1 of these genesSLC4A1About this report →
- Hepatic Porphyria DisordersReads 1 of these genesALAS2About this report →
- Hereditary Sideroblastic AnaemiasReads 1 of these genesALAS2About this report →
- Red Blood Cell Membrane DisordersReads 1 of these genesSLC4A1About this report →
- PorphyriaReads 1 of these genesALAS2About this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesHACE1About this report →
- Epilepsy (Full Panel)Reads 1 of these genesHACE1About this report →
- Intellectual DisabilityReads 1 of these genesSMAD4About this report →
- Inherited Neurodegenerative DisordersReads 1 of these genesHACE1About this report →
Læs de gener, der er knyttet til Anemic pallor, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test16 gener knyttet til Anemic pallor
Ændringer i disse gener forårsager sjældne tilstande, hvor Anemic pallor 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 |
|---|---|---|
| ALAS25'-aminolevulinate synthase 2 | Altid | I 1 tilstand |
| BMPR1Abone morphogenetic protein receptor type 1A | Ofte (30–79 %) | I 1 tilstand |
| ENGendoglin | Ofte (30–79 %) | I 1 tilstand |
| SLC4A1solute carrier family 4 member 1 (Diego blood group) | Ofte (30–79 %) | I 1 tilstand |
| SMAD4SMAD family member 4 | Ofte (30–79 %) | I 1 tilstand |
| ALKALK receptor tyrosine kinase | Nogle gange (5–29 %) | I 1 tilstand |
| HACE1HECT domain and ankyrin repeat containing E3 ubiquitin protein ligase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| LIN28Blin-28 RNA binding posttranscriptional regulator B | Nogle gange (5–29 %) | I 1 tilstand |
| LMO1LIM domain only 1 | Nogle gange (5–29 %) | I 1 tilstand |
| MYCNMYCN proto-oncogene, bHLH transcription factor | Nogle gange (5–29 %) | I 1 tilstand |
| PHOX2Bpaired like homeobox 2B | Nogle gange (5–29 %) | I 1 tilstand |
| TMPRSS6transmembrane serine protease 6 | Nogle gange (5–29 %) | I 1 tilstand |
| FANCAFA complementation group A | Ikke registreret | I 1 tilstand |
| FANCCFA complementation group C | Ikke registreret | I 1 tilstand |
| FANCD2FA complementation group D2 | Ikke registreret | I 1 tilstand |
| FANCEFA complementation group E | 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 2026.10.19-9814e911.
AtlasFrom 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.
Gratis forsendelse · Resultater på 6–8 uger
