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Traits
Traits linked to MCFD2
multiple coagulation factor deficiency 2, ER cargo receptor complex subunit
The Human Phenotype Ontology links 19 traits to MCFD2, 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 |
|---|---|
| Prolonged partial thromboplastin time | Very often (80–99%) |
| Prolonged prothrombin time | Very often (80–99%) |
| Reduced coagulation factor V activity | Very often (80–99%) |
| Reduced factor VIII activity | Very often (80–99%) |
| Bleeding gums | Often (30–79%) |
| Bleeding with minor or no trauma | Often (30–79%) |
| Bloody nose | Often (30–79%) |
| Bruising susceptibility | Often (30–79%) |
| Prolonged bleeding after dental extraction | Often (30–79%) |
| Prolonged bleeding following circumcision | Often (30–79%) |
| Abnormally heavy bleeding during menstruation | Sometimes (5–29%) |
| Bleeding within a joint | Sometimes (5–29%) |
| Bleeding within the skull | Sometimes (5–29%) |
| Gastrointestinal bleeding | Sometimes (5–29%) |
| Prolonged bleeding after surgery | Sometimes (5–29%) |
| Excessive bleeding after minor trauma | Not recorded |
Laboratory abnormality
| Trait | How often it is seen |
|---|---|
| Blood in urine | Sometimes (5–29%) |
| Elevated lipids in blood | Rarely (1–4%) |
| High blood uric acid level | Rarely (1–4%) |
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 MCFD2 and how often each is seen. Find out more at hpo.jax.org.
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