AtlasEgenskap
Fatty deposits in skin around the eyes
Klinisk navn: Xanthelasma
The presence of xanthomata in the skin of the eyelid.
Sammendrag
- Også kalt
- Fatty deposits on eyelids, Xanthelasma palpebrarum, Xanthoma
AtlasDenne siden som data
Legg til .json etter adressen til siden, eller be om application/json, for å lese den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/xanthelasma.json"
page <- fromJSON(url)
page$trait$nameLes genene knyttet til Fatty deposits in skin around the eyes, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test24 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.
- HyperlipidemiaReads 6 of these genesABCG8APOELPLAPOBLDLRPCSK9About this report →
- Familial HypercholesterolemiaReads 3 of these genesAPOBLDLRPCSK9About this report →
- Hereditary HypolipoproteinemiasReads 3 of these genesABCA1APOA1APOBAbout this report →
- Cerebrotendinous XanthomatosisReads 1 of these genesCYP27A1About this report →
Show 20 more reports
- Hereditary FibromatosesReads 1 of these genesPDGFRBAbout this report →
- STAT1 and STAT3 Gain-of-Function DiseaseReads 1 of these genesSTAT3About this report →
- Glycogen Storage DiseaseReads 2 of these genesSLC37A4G6PC1About this report →
- Alzheimer diseaseReads 1 of these genesAPOEAbout this report →
- Growth Hormone Insensitivity & IGF-1 Axis DisordersReads 1 of these genesGHRAbout this report →
- Basal Ganglia CalcificationReads 1 of these genesPDGFRBAbout this report →
- Hyper-IgE SyndromeReads 1 of these genesSTAT3About this report →
- Mendelian Susceptibility to Mycobacterial Disease (MSMD)Reads 1 of these genesIL12RB1About this report →
- Hereditary AmyloidosisReads 1 of these genesAPOA1About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 2 of these genesCYP27A1TTPAAbout this report →
- Autoimmune DiseaseReads 1 of these genesSTAT3About this report →
- Noonan SyndromeReads 1 of these genesSPRED1About this report →
- Rare Hereditary Peripheral NeuropathiesReads 3 of these genesAPOA1CYP27A1TTPAAbout this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesTNPO3About this report →
- Inherited Neurodegenerative DisordersReads 3 of these genesAPOECYP27A1TTPAAbout this report →
- Lysosomal Storage DiseaseReads 1 of these genesCYP27A1About this report →
- Hypertrophic CardiomyopathyReads 1 of these genesSPRED1About this report →
- Other Inherited LeukodystrophiesReads 1 of these genesCYP27A1About this report →
- Congenital Disorders of GlycosylationReads 1 of these genesSLC37A4About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesSTAT3About this report →
Les genene knyttet til Fatty deposits in skin around the eyes, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test27 gener knyttet til Fatty deposits in skin around the eyes
Endringer i disse genene forårsaker sjeldne tilstander der Fatty deposits in skin around the eyes forekommer. De fleste med denne egenskapen har ingen av disse tilstandene, og et gen på denne listen sier ingenting om noens eget genom.
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| ABCG8ATP binding cassette subfamily G member 8 | Alltid | I 1 tilstand |
| ABCA1ATP binding cassette subfamily A member 1 | Ofte (30–79 %) | I 1 tilstand |
| APOA1apolipoprotein A1 | Ofte (30–79 %) | I 1 tilstand |
| APOEapolipoprotein E | Ofte (30–79 %) | I 1 tilstand |
| IL12Ainterleukin 12A | Ofte (30–79 %) | I 1 tilstand |
| IL12RB1interleukin 12 receptor subunit beta 1 | Ofte (30–79 %) | I 1 tilstand |
| IRF5interferon regulatory factor 5 | Ofte (30–79 %) | I 1 tilstand |
| MMEL1membrane metalloendopeptidase like 1 | Ofte (30–79 %) | I 1 tilstand |
| PDGFRBplatelet derived growth factor receptor beta | Ofte (30–79 %) | I 1 tilstand |
| POU2AF1POU class 2 homeobox associating factor 1 | Ofte (30–79 %) | I 1 tilstand |
| SPIBSpi-B transcription factor | Ofte (30–79 %) | I 1 tilstand |
| STAT3signal transducer and activator of transcription 3 | Ofte (30–79 %) | I 1 tilstand |
| TNFSF15TNF superfamily member 15 | Ofte (30–79 %) | I 1 tilstand |
| TNPO3transportin 3 | Ofte (30–79 %) | I 1 tilstand |
| LPLlipoprotein lipase | Noen ganger (5–29 %) | I 1 tilstand |
| SLC37A4solute carrier family 37 member 4 | Noen ganger (5–29 %) | I 3 tilstander |
| SPRED1sprouty related EVH1 domain containing 1 | Sjelden (1–4%) | I 1 tilstand |
| APOA2apolipoprotein A2 | Ikke registrert | I 1 tilstand |
| APOBapolipoprotein B | Ikke registrert | I 1 tilstand |
| CYP27A1cytochrome P450 family 27 subfamily A member 1 | Ikke registrert | I 1 tilstand |
| EPHX2epoxide hydrolase 2 | Ikke registrert | I 1 tilstand |
| G6PC1glucose-6-phosphatase catalytic subunit 1 | Ikke registrert | I 1 tilstand |
| GHRgrowth hormone receptor | Ikke registrert | I 1 tilstand |
| LDLRlow density lipoprotein receptor | Ikke registrert | I 1 tilstand |
| PCSK9proprotein convertase subtilisin/kexin type 9 | Ikke registrert | I 1 tilstand |
| PPP1R17protein phosphatase 1 regulatory subunit 17 | Ikke registrert | I 1 tilstand |
| TTPAalpha tocopherol transfer protein | Ikke registrert | I 1 tilstand |
Hvor ofte dette forekommer hos personer med en av genets tilstander, oppgitt som den hyppigste forekomsten blant dem, slik Human Phenotype Ontology registrerer den. Disse sidene beskriver egenskaper og forskningen bak dem. De er ikke en diagnose, og om symptomer bør du spørre lege eller genetisk rådgiver.
Bredere egenskaper
Slik er informasjonen samlet
- Human Phenotype Ontology, versjon 2026-09-01: egenskapen, navnene på den, definisjonen og genene som er knyttet til den. Les mer på hpo.jax.org.
- Datautgave 2026.10.19-9814e911.
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