familial ossifying fibroma
MONDO:0007660Mondo
Findings
No curated finding names familial ossifying fibroma yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
An instance of ossifying fibroma (disease) that is caused by an inherited modification of the individual's genome.
Definition from the Mondo Disease Ontology (MONDO:0007660), read 2026-09-29. CC BY 4.0.
Where it sits
Other names
2 names
Resolves to: familial ossifying fibroma
- Also called
- hereditary ossifying fibroma (disease)multiple ossifying fibroma