Trait
Cephalohematoma
Hemorrhage between the skull and periosteum of a newborn resulting from rupture of blood vessels that cross the periosteum.
Summary
- Also called
- Cephalohaematoma
Reference genomeGRCh38hg38
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Read the genes linked to Cephalohematoma, and the rest of your genome, with one test.
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Get my Genome Test13 genes linked to Cephalohematoma
Changes in these genes cause rare conditions in which Cephalohematoma 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 |
|---|---|---|
| CD109CD109 molecule | Often (30–79%) | In 1 condition |
| EMILIN1elastin microfibril interfacer 1 | Often (30–79%) | In 1 condition |
| GP1BAglycoprotein Ib platelet subunit alpha | Often (30–79%) | In 1 condition |
| GP1BBglycoprotein Ib platelet subunit beta | Often (30–79%) | In 1 condition |
| ITGA2integrin subunit alpha 2 | Often (30–79%) | In 1 condition |
| ITGA2Bintegrin subunit alpha 2b | Often (30–79%) | In 1 condition |
| ITGB3integrin subunit beta 3 | Often (30–79%) | In 1 condition |
| AXIN1axin 1 | Sometimes (5–29%) | In 1 condition |
| CDC42BPBCDC42 binding protein kinase beta | Sometimes (5–29%) | In 1 condition |
| F2coagulation factor II, thrombin | Sometimes (5–29%) | In 1 condition |
| F8coagulation factor VIII | Sometimes (5–29%) | In 1 condition |
| GGCXgamma-glutamyl carboxylase | Sometimes (5–29%) | In 1 condition |
| VKORC1vitamin K epoxide reductase complex subunit 1 | 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.
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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