Trait
Mastoiditis
Infection of the mastoid air cells, arising as a complication of otitis media or occurring in the context of unusual susceptibility to infection.
Summary
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Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.
- Otofaciocervical Syndrome Type 2 (PAX1)Reads 1 of these genesPAX1About this report →
- Hereditary Manganese Transporter DisordersReads 1 of these genesSLC39A14About this report →
- Other Inborn Errors of ImmunityReads 6 of these genesIRF4ITPR3MALT1TPP2RAG1RAG2About this report →
- Severe Combined ImmunodeficiencyReads 2 of these genesRAG1RAG2About this report →
Show 4 more reports
- Rare Monogenic Autoinflammatory DiseasesReads 1 of these genesDOCK11About this report →
- DNA Repair DiseaseReads 1 of these genesNBNAbout this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesITPR3About this report →
- Rare Hereditary Peripheral NeuropathiesReads 1 of these genesITPR3About this report →
Read the genes linked to Mastoiditis, and the rest of your genome, with one test.
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Get my Genome Test10 genes linked to Mastoiditis
Changes in these genes cause rare conditions in which Mastoiditis 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 |
|---|---|---|
| IRF4interferon regulatory factor 4 | Always | In 1 condition |
| ITPR3inositol 1,4,5-trisphosphate receptor type 3 | Always | In 1 condition |
| MALT1MALT1 paracaspase | Always | In 1 condition |
| DOCK11dedicator of cytokinesis 11 | Sometimes (5–29%) | In 1 condition |
| PAX1paired box 1 | Sometimes (5–29%) | In 1 condition |
| TPP2tripeptidyl peptidase 2 | Sometimes (5–29%) | In 1 condition |
| SLC39A14solute carrier family 39 member 14 | Rarely (1–4%) | In 1 condition |
| NBNnibrin | Not recorded | In 1 condition |
| RAG1recombination activating 1 | Not recorded | In 1 condition |
| RAG2recombination activating 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 2026.10.18-e609d43e.
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