Trait
Facial telangiectasia
Telangiectases (small dilated blood vessels) located near the surface of the skin of the face.
Summary
- Also called
- Facial telangiectatic vessels, Telangiectasia, facial
Share this page
This page as data
Add .json to the page's address, or ask for application/json, to read it as JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/facial-telangiectasia.json"
page <- fromJSON(url)
page$trait$nameRead the genes linked to Facial telangiectasia, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome Test12 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.
- H SyndromeReads 1 of these genesSLC29A3About this report →
- Hereditary Hemorrhagic TelangiectasiaReads 1 of these genesACVRL1About this report →
- Hypodontia and AnodontiaReads 1 of these genesWNT10AAbout this report →
- Hereditary Pheochromocytoma and ParagangliomaReads 1 of these genesSDHDAbout this report →
Show 8 more reports
- Ectodermal DysplasiasReads 1 of these genesWNT10AAbout this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 1 of these genesATRXAbout this report →
- Pontocerebellar Hypoplasia (TSEN54 and MINPP1)Reads 1 of these genesVPS53About this report →
- Lissencephaly Spectrum DisordersReads 1 of these genesARXAbout this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 1 of these genesWNT10AAbout this report →
- Hearing Loss and DeafnessReads 1 of these genesOSBPL2About this report →
- Epilepsy (Full Panel)Reads 1 of these genesARXAbout this report →
- Intellectual DisabilityReads 1 of these genesATRXAbout this report →
Read the genes linked to Facial telangiectasia, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome Test11 genes linked to Facial telangiectasia
Changes in these genes cause rare conditions in which Facial telangiectasia is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.
| Gene | How often it is seen | Conditions |
|---|---|---|
| ATRATR checkpoint kinase | Always | In 1 condition |
| OSBPL2oxysterol binding protein like 2 | Always | In 1 condition |
| VPS53VPS53 subunit of GARP complex | Always | In 1 condition |
| ACVRL1activin A receptor like type 1 | Very often (80–99%) | In 1 condition |
| WNT10AWnt family member 10A | Very often (80–99%) | In 1 condition |
| SLC29A3solute carrier family 29 member 3 | Often (30–79%) | In 2 conditions |
| ARPC4actin related protein 2/3 complex subunit 4 | Sometimes (5–29%) | In 1 condition |
| ARXaristaless related homeobox | Sometimes (5–29%) | In 1 condition |
| SDHDsuccinate dehydrogenase complex subunit D | Sometimes (5–29%) | In 1 condition |
| TTI1TELO2 interacting protein 1 | Sometimes (5–29%) | In 1 condition |
| ATRXATRX chromatin remodeler | Rarely (1–4%) | In 1 condition |
How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.
Narrower traits
Broader traits
Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
- Data release 2026.10.19-9814e911.
From 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.
Free shipping · Results in 6–8 weeks
