Trait
Splenic infarction
Ischemia and necrosis of part or all of the spleen resulting from compromise of blood supply resulting from arterial or venous occlusion.
Summary
- Also called
- Spleen infarct, Spleen infarction, Splenic infarct
Reference genomeGRCh38hg38
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Get my Genome Test8 genes linked to Splenic infarction
Changes in these genes cause rare conditions in which Splenic infarction 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 |
|---|---|---|
| F8coagulation factor VIII | Always | In 1 condition |
| BCL11ABCL11 transcription factor A | Sometimes (5–29%) | In 1 condition |
| GBA1glucosylceramidase beta 1 | Sometimes (5–29%) | In 1 condition |
| HBBhemoglobin subunit beta | Sometimes (5–29%) | In 3 conditions |
| HBG1hemoglobin subunit gamma 1 | Sometimes (5–29%) | In 1 condition |
| HBG2hemoglobin subunit gamma 2 | Sometimes (5–29%) | In 1 condition |
| KLF1KLF transcription factor 1 | Sometimes (5–29%) | In 1 condition |
| SCARB2scavenger receptor class B member 2 | 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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