AtlasEgenskap
Facial puffiness
Klinisk navn: Facial edema
Sammendrag
- Også kalt
- Facial swelling, Facial oedema, Swelling of the face
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/facial-edema.json"
page <- fromJSON(url)
page$trait$nameLes genene knyttet til Facial puffiness, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test28 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.
- Congenital HypothyroidismReads 13 of these genesFOXE1NKX2-1NKX2-5PAX8SLC26A4TSHBAbout this report →
- Thyroid CancerReads 12 of these genesNKX2-5PAX8SLC26A4TSHBTSHRALBAbout this report →
- Hereditary AngioedemaReads 3 of these genesSERPING1F12PLGAbout this report →
- HyperthyroidismReads 2 of these genesTSHRALBAbout this report →
Show 24 more reports
- Rothmund-Thomson SyndromeReads 2 of these genesANAPC1RECQL4About this report →
- Congenital AnalbuminaemiaReads 1 of these genesALBAbout this report →
- Congenital Factor XII DeficiencyReads 1 of these genesF12About this report →
- High-Molecular-Weight Kininogen DeficiencyReads 1 of these genesKNG1About this report →
- Pendred SyndromeReads 1 of these genesSLC26A4About this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 5 of these genesHESX1LHX3LHX4POU1F1PROP1About this report →
- Primary Lymphoedema & Lymphatic MalformationsReads 3 of these genesEPHB4GJC2PIEZO1About this report →
- Hypogonadotropic HypogonadismReads 5 of these genesHESX1LHX3LHX4POU1F1PROP1About this report →
- Tetralogy of FallotReads 1 of these genesNKX2-5About this report →
- Hereditary Vascular MalformationsReads 1 of these genesEPHB4About this report →
- Inherited Fibrinolytic DisordersReads 1 of these genesPLGAbout this report →
- Syndromic and Metabolic CardiomyopathiesReads 1 of these genesNKX2-5About this report →
- Alpha-Mannosidosis and Other GlycoproteinosesReads 1 of these genesNEU1About this report →
- Hyper-IgE SyndromeReads 1 of these genesSPINK5About this report →
- Red Blood Cell Membrane DisordersReads 1 of these genesPIEZO1About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesNKX2-5About this report →
- Syndromic CraniosynostosisReads 1 of these genesRECQL4About this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 1 of these genesGJC2About this report →
- Lysosomal Storage DiseaseReads 1 of these genesNEU1About this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesGJC2About this report →
- Other Inherited LeukodystrophiesReads 1 of these genesGJC2About this report →
- Hearing Loss and DeafnessReads 1 of these genesSLC26A4About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesSPINK5About this report →
- Inherited Neurodegenerative DisordersReads 1 of these genesGJC2About this report →
Les genene knyttet til Facial puffiness, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test35 gener knyttet til Facial puffiness
Endringer i disse genene forårsaker sjeldne tilstander der Facial puffiness 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 |
|---|---|---|
| MYOFmyoferlin | Alltid | I 1 tilstand |
| SPINK5serine peptidase inhibitor Kazal type 5 | Alltid | I 1 tilstand |
| KNG1kininogen 1 | Svært ofte (80–99 %) | I 1 tilstand |
| SERPING1serpin family G member 1 | Svært ofte (80–99 %) | I 1 tilstand |
| XPNPEP2X-prolyl aminopeptidase 2 | Svært ofte (80–99 %) | I 1 tilstand |
| FOXE1forkhead box E1 | Ofte (30–79 %) | I 1 tilstand |
| HESX1HESX homeobox 1 | Ofte (30–79 %) | I 1 tilstand |
| LHX3LIM homeobox 3 | Ofte (30–79 %) | I 1 tilstand |
| LHX4LIM homeobox 4 | Ofte (30–79 %) | I 1 tilstand |
| NKX2-1NK2 homeobox 1 | Ofte (30–79 %) | I 1 tilstand |
| NKX2-5NK2 homeobox 5 | Ofte (30–79 %) | I 1 tilstand |
| PAX8paired box 8 | Ofte (30–79 %) | I 1 tilstand |
| POU1F1POU class 1 homeobox 1 | Ofte (30–79 %) | I 1 tilstand |
| PROP1PROP paired-like homeobox 1 | Ofte (30–79 %) | I 1 tilstand |
| SLC26A4solute carrier family 26 member 4 | Ofte (30–79 %) | I 1 tilstand |
| TSHBthyroid stimulating hormone subunit beta | Ofte (30–79 %) | I 1 tilstand |
| TSHRthyroid stimulating hormone receptor | Ofte (30–79 %) | I 1 tilstand |
| ALBalbumin | Noen ganger (5–29 %) | I 1 tilstand |
| ANAPC1anaphase promoting complex subunit 1 | Noen ganger (5–29 %) | I 1 tilstand |
| DUOX2dual oxidase 2 | Noen ganger (5–29 %) | I 1 tilstand |
| DUOXA2dual oxidase maturation factor 2 | Noen ganger (5–29 %) | I 1 tilstand |
| EPHB4EPH receptor B4 | Noen ganger (5–29 %) | I 2 tilstander |
| GJC2gap junction protein gamma 2 | Noen ganger (5–29 %) | I 1 tilstand |
| IYDiodotyrosine deiodinase | Noen ganger (5–29 %) | I 1 tilstand |
| RECQL4RecQ like helicase 4 | Noen ganger (5–29 %) | I 1 tilstand |
| SLC5A5solute carrier family 5 member 5 | Noen ganger (5–29 %) | I 1 tilstand |
| TGthyroglobulin | Noen ganger (5–29 %) | I 1 tilstand |
| TPOthyroid peroxidase | Noen ganger (5–29 %) | I 1 tilstand |
| HAVCR2hepatitis A virus cellular receptor 2 | Sjelden (1–4%) | I 1 tilstand |
| ANGPT1angiopoietin 1 | Ikke registrert | I 1 tilstand |
| F12coagulation factor XII | Ikke registrert | I 1 tilstand |
| HS3ST6heparan sulfate-glucosamine 3-sulfotransferase 6 | Ikke registrert | I 1 tilstand |
| NEU1neuraminidase 1 | Ikke registrert | I 1 tilstand |
| PIEZO1piezo type mechanosensitive ion channel component 1 (Er blood group) | Ikke registrert | I 1 tilstand |
| PLGplasminogen | 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.
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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.
AtlasFrom traits to your genome
Read the genes behind these traits in your own DNA.
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