Trait
Ossifying fibroma
A benign central bone tumor composed of fibrous connective tissue within which bone is formed.
Summary
- Body system
- Abnormal tissue mass
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Get my Genome Test1 gene linked to Ossifying fibroma
Changes in these genes cause rare conditions in which Ossifying fibroma 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 |
|---|---|---|
| NF1neurofibromin 1 | Rarely (1–4%) | 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.
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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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