Trait
Progressive leukoencephalopathy
Leukoencephalopathy that gets more severe with time.
Summary
- Also called
- Leukoencephalopathy, progressive
- Body system
- Abnormality of the nervous system
Reference genomeGRCh38hg38
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Get my Genome Test5 genes linked to Progressive leukoencephalopathy
Changes in these genes cause rare conditions in which Progressive leukoencephalopathy 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 |
|---|---|---|
| KIF5Akinesin family member 5A | Always | In 1 condition |
| PLAAphospholipase A2 activating protein | Always | In 1 condition |
| COA8cytochrome c oxidase assembly factor 8 | Very often (80–99%) | In 1 condition |
| AARS2alanyl-tRNA synthetase 2, mitochondrial | Not recorded | In 1 condition |
| SDHAsuccinate dehydrogenase complex flavoprotein subunit A | Not recorded | 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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