Trait
Subdural hemorrhage
Hemorrhage occurring between the dura mater and the arachnoid mater.
Summary
- Also called
- Subdural haematoma, Subdural haemorrhage, Subdural hematoma
Reference genomeGRCh38hg38
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Get my Genome Test17 genes linked to Subdural hemorrhage
Changes in these genes cause rare conditions in which Subdural hemorrhage 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 |
|---|---|---|
| ACTA1actin alpha 1, skeletal muscle | Always | In 1 condition |
| GTPBP2GTP binding protein 2 | Always | In 1 condition |
| ITGA2Bintegrin subunit alpha 2b | Always | In 1 condition |
| SPOUT1SPOUT domain containing methyltransferase 1 | Always | In 1 condition |
| GCDHglutaryl-CoA dehydrogenase | Very often (80–99%) | In 2 conditions |
| BICD2BICD cargo adaptor 2 | Often (30–79%) | In 1 condition |
| DNM2dynamin 2 | Often (30–79%) | In 1 condition |
| RBM10RNA binding motif protein 10 | Often (30–79%) | In 1 condition |
| F8coagulation factor VIII | Sometimes (5–29%) | In 2 conditions |
| FGAfibrinogen alpha chain | Sometimes (5–29%) | In 1 condition |
| FGBfibrinogen beta chain | Sometimes (5–29%) | In 1 condition |
| FGGfibrinogen gamma chain | Sometimes (5–29%) | In 1 condition |
| MMACHCmetabolism of cobalamin associated C | Sometimes (5–29%) | In 1 condition |
| STT3ASTT3 oligosaccharyltransferase complex catalytic subunit A | Sometimes (5–29%) | In 1 condition |
| ZFXzinc finger protein X-linked | Sometimes (5–29%) | In 1 condition |
| ERCC6ERCC excision repair 6, chromatin remodeling factor | Rarely (1–4%) | In 1 condition |
| ERCC8ERCC excision repair 8, CSA ubiquitin ligase complex subunit | 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.
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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