Familial ossifying fibroma

MONDO:0007660

An instance of ossifying fibroma (disease) that is caused by an inherited modification of the individual's genome.

Also known as: hereditary ossifying fibroma (disease), multiple ossifying fibroma, Cementomas, familial multiple, GIGANTIFORM cementoma, familial, Jaffe-Campanacci syndrome, cemental dysplasia, periapical, intracortical fibrous dysplasia

1445 clinical trials for this condition and its sub-types, 0 tagged with Familial ossifying fibroma itself.

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↑ Hereditary disorder of connective tissue (1314) ↑ Ossifying fibroma (0)

Including sub-types (1445) Tagged with Familial ossifying fibroma (0)

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