Trait
Recurrent Aspergillus infection
Increased susceptibility to Aspergillus infections as manifested by recurrent episodes of Aspergillus infection.
Summary
- Also called
- Aspergillus infections, recurrent, Chronic aspergillosis, Persistent aspergillus infection, Recurrent aspergillosis, Recurrent Aspergillus infections
- Body system
- Abnormality of the immune system
Reference genomeGRCh38hg38
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Get my Genome Test24 genes linked to Recurrent Aspergillus infection
Changes in these genes cause rare conditions in which Recurrent Aspergillus infection 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 |
|---|---|---|
| CEACAM3CEA cell adhesion molecule 3 | Sometimes (5–29%) | In 1 condition |
| CEACAM6CEA cell adhesion molecule 6 | Sometimes (5–29%) | In 1 condition |
| CFTRCF transmembrane conductance regulator | Sometimes (5–29%) | In 1 condition |
| CLCA4chloride channel accessory 4 | Sometimes (5–29%) | In 1 condition |
| DCTN4dynactin subunit 4 | Sometimes (5–29%) | In 1 condition |
| EDNRAendothelin receptor type A | Sometimes (5–29%) | In 1 condition |
| GCLCglutamate-cysteine ligase catalytic subunit | Sometimes (5–29%) | In 1 condition |
| GSTM3glutathione S-transferase mu 3 | Sometimes (5–29%) | In 1 condition |
| HFEhomeostatic iron regulator | Sometimes (5–29%) | In 1 condition |
| HMOX1heme oxygenase 1 | Sometimes (5–29%) | In 1 condition |
| KCNN4potassium calcium-activated channel subfamily N member 4 | Sometimes (5–29%) | In 1 condition |
| MIFmacrophage migration inhibitory factor | Sometimes (5–29%) | In 1 condition |
| SERPINA1serpin family A member 1 | Sometimes (5–29%) | In 1 condition |
| SLC11A1solute carrier family 11 member 1 | Sometimes (5–29%) | In 1 condition |
| SLC26A9solute carrier family 26 member 9 | Sometimes (5–29%) | In 1 condition |
| SLC6A14solute carrier family 6 member 14 | Sometimes (5–29%) | In 1 condition |
| SLC9A3solute carrier family 9 member A3 | Sometimes (5–29%) | In 1 condition |
| STAT1signal transducer and activator of transcription 1 | Sometimes (5–29%) | In 1 condition |
| STX1Asyntaxin 1A | Sometimes (5–29%) | In 1 condition |
| TGFB1transforming growth factor beta 1 | Sometimes (5–29%) | In 1 condition |
| CYBAcytochrome b-245 alpha chain | Not recorded | In 1 condition |
| CYBBcytochrome b-245 beta chain | Not recorded | In 1 condition |
| NCF1neutrophil cytosolic factor 1 | Not recorded | In 1 condition |
| NCF2neutrophil cytosolic factor 2 | 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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