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Traits
Traits linked to SERPINC1
serpin family C member 1
The Human Phenotype Ontology links 15 traits to SERPINC1, by body system: features seen in people with one of the gene's rare conditions.
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Abnormality of blood and blood-forming tissues
| Trait | How often it is seen |
|---|---|
| Decreased level of heparin co-factor II | Always |
| Recurrent thrombophlebitis | Always |
| Reduced antithrombin antigen | Very often (80–99%) |
| Reduced antithrombin III activity | Very often (80–99%) |
| Blood clot in a deep vein | Often (30–79%) |
| Recurrent thromboembolism | Often (30–79%) |
| Superficial thrombophlebitis | Often (30–79%) |
| Blood clot in artery | Sometimes (5–29%) |
| Blood clot in liver vein | Sometimes (5–29%) |
| Blood clot in portal vein | Sometimes (5–29%) |
| Mesenteric venous thrombosis | Sometimes (5–29%) |
| Blood clot in cerebral vein | Rarely (1–4%) |
Abnormality of the cardiovascular system
| Trait | How often it is seen |
|---|---|
| Blood clot in artery of lung | Often (30–79%) |
| Retinal venous occlusion | Sometimes (5–29%) |
| Arterial occlusion | Not recorded |
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.
Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to SERPINC1 and how often each is seen. Find out more at hpo.jax.org.
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