Trait
Persistent CMV viremia
Persistent or recurrent detection of cytomegalovirus (CMV) in the blood that occurs in the context of unusual susceptibility to infection.
Summary
- Also called
- Chronic CMV viremia, Persistent CMV viraemia, Recurrent CMV viremia
Reference genomeGRCh38hg38
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Get my Genome Test8 genes linked to Persistent CMV viremia
Changes in these genes cause rare conditions in which Persistent CMV viremia 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 |
|---|---|---|
| CD28CD28 molecule | Always | In 1 condition |
| IL2RBinterleukin 2 receptor subunit beta | Always | In 1 condition |
| LATlinker for activation of T cells | Always | In 1 condition |
| MAGT1magnesium transporter 1 | Always | In 1 condition |
| RELREL proto-oncogene, NF-kB subunit | Always | In 1 condition |
| TPP2tripeptidyl peptidase 2 | Often (30–79%) | In 1 condition |
| PIK3CDphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | Sometimes (5–29%) | In 1 condition |
| PIK3R1phosphoinositide-3-kinase regulatory subunit 1 | Sometimes (5–29%) | In 2 conditions |
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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