Trait
Internal bleeding
Clinical name: Internal hemorrhage
The presence of hemorrhage within the body.
Summary
- Also called
- Internal haemorrhage
Reference genomeGRCh38hg38
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Get my Genome Test11 genes linked to Internal bleeding
Changes in these genes cause rare conditions in which Internal bleeding 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 |
|---|---|---|
| WASWASP actin nucleation promoting factor | Very often (80–99%) | In 1 condition |
| COL3A1collagen type III alpha 1 chain | Often (30–79%) | In 1 condition |
| AGGF1angiogenic factor with G-patch and FHA domains 1 | Sometimes (5–29%) | In 1 condition |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Sometimes (5–29%) | In 1 condition |
| CD46CD46 molecule | Rarely (1–4%) | In 1 condition |
| CFHcomplement factor H | Rarely (1–4%) | In 1 condition |
| CFIcomplement factor I | Rarely (1–4%) | In 1 condition |
| HELLPARHELLP associated long non-coding RNA | Rarely (1–4%) | In 1 condition |
| IFNGinterferon gamma | Rarely (1–4%) | In 1 condition |
| TSC1TSC complex subunit 1 | Rarely (1–4%) | In 1 condition |
| TSC2TSC complex subunit 2 | 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.
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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 2026.10.16-c6eea6bf.
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