Trait
Prolonged bleeding after surgery
Bleeding that persists longer than the normal time following a surgical procedure.
Summary
- Also called
- Excessive bleeding during surgery, Protracted bleeding after surgery
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome Test23 genes linked to Prolonged bleeding after surgery
Changes in these genes cause rare conditions in which Prolonged bleeding after surgery 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 |
|---|---|---|
| F10coagulation factor X | Always | In 2 conditions |
| ANO6anoctamin 6 | Very often (80–99%) | In 1 condition |
| SERPINE1serpin family E member 1 | Very often (80–99%) | In 1 condition |
| F13Bcoagulation factor XIII B chain | Often (30–79%) | In 2 conditions |
| F7coagulation factor VII | Often (30–79%) | In 1 condition |
| F8coagulation factor VIII | Often (30–79%) | In 3 conditions |
| ITGA2Bintegrin subunit alpha 2b | Often (30–79%) | In 2 conditions |
| ITGB3integrin subunit beta 3 | Often (30–79%) | In 3 conditions |
| VWFvon Willebrand factor | Often (30–79%) | In 2 conditions |
| ACTN1actinin alpha 1 | Sometimes (5–29%) | In 1 condition |
| F13A1coagulation factor XIII A chain | Sometimes (5–29%) | In 1 condition |
| F5coagulation factor V | Sometimes (5–29%) | In 1 condition |
| GFI1Bgrowth factor independent 1B transcriptional repressor | Sometimes (5–29%) | In 1 condition |
| GP1BAglycoprotein Ib platelet subunit alpha | Sometimes (5–29%) | In 3 conditions |
| GP1BBglycoprotein Ib platelet subunit beta | Sometimes (5–29%) | In 3 conditions |
| GP9glycoprotein IX platelet | Sometimes (5–29%) | In 2 conditions |
| LMAN1lectin, mannose binding 1 | Sometimes (5–29%) | In 1 condition |
| MCFD2multiple coagulation factor deficiency 2, ER cargo receptor complex subunit | Sometimes (5–29%) | In 1 condition |
| TPM4tropomyosin 4 | Sometimes (5–29%) | In 2 conditions |
| TRPM7transient receptor potential cation channel subfamily M member 7 | Sometimes (5–29%) | In 1 condition |
| TUBA8tubulin alpha 8 | Sometimes (5–29%) | In 1 condition |
| TUBB1tubulin beta 1 class VI | Sometimes (5–29%) | In 1 condition |
| P2RY12purinergic receptor P2Y12 | Not recorded | 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.
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 2026.10.16-c6eea6bf.
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