Trait
Splenic rupture
A breach of the capsule of the spleen.
Summary
- Also called
- Ruptured spleen
Reference genomeGRCh38hg38
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Get my Genome Test6 genes linked to Splenic rupture
Changes in these genes cause rare conditions in which Splenic rupture 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 |
|---|---|---|
| COL3A1collagen type III alpha 1 chain | Sometimes (5–29%) | In 1 condition |
| 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 |
| GBA1glucosylceramidase beta 1 | Rarely (1–4%) | In 1 condition |
| SCARB2scavenger receptor class B member 2 | 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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