Trait
Bleeding below the skin
Clinical name: Subcutaneous hemorrhage
This term refers to an abnormally increased susceptibility to bruising (purpura, petechiae, or ecchymoses).
Summary
- Also called
- Subcutaneous haemorrhage
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/subcutaneous-hemorrhage.json"
page <- fromJSON(url)
page$trait$nameRead the genes linked to Bleeding below the skin, and the rest of your genome, with one test.
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Get my Genome Test15 genes linked to Bleeding below the skin
Changes in these genes cause rare conditions in which Bleeding below the skin 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 |
|---|---|---|
| EPHB2EPH receptor B2 | Always | In 1 condition |
| ADAMTS2ADAM metallopeptidase with thrombospondin type 1 motif 2 | Very often (80–99%) | In 1 condition |
| ADAMTSL2ADAMTS like 2 | Very often (80–99%) | In 1 condition |
| ARL6IP6ARF like GTPase 6 interacting protein 6 | Very often (80–99%) | In 1 condition |
| CHST14carbohydrate sulfotransferase 14 | Very often (80–99%) | In 1 condition |
| DSEdermatan sulfate epimerase | Very often (80–99%) | In 1 condition |
| GNA11G protein subunit alpha 11 | Very often (80–99%) | In 1 condition |
| SLC35A1solute carrier family 35 member A1 | Very often (80–99%) | In 2 conditions |
| F13A1coagulation factor XIII A chain | Often (30–79%) | In 1 condition |
| F13Bcoagulation factor XIII B chain | Often (30–79%) | In 1 condition |
| F8coagulation factor VIII | Often (30–79%) | In 1 condition |
| PROS1protein S | Often (30–79%) | In 1 condition |
| PTENphosphatase and tensin homolog | Often (30–79%) | In 1 condition |
| SERPINE1serpin family E member 1 | Often (30–79%) | In 1 condition |
| CBScystathionine beta-synthase | Sometimes (5–29%) | 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.
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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 2026.10.17-8666dff2.
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