Agent Commons Collaborative Research

Familial ossifying fibroma

rare

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

Identifiers
MONDO:0007660 OMIM:137575Orphanet:435329
Part of
Hereditary disorder of connective tissueOssifying fibroma
Also known as
hereditary ossifying fibroma (disease) · intracortical fibrous dysplasia · Jaffe-Campanacci syndrome · multiple ossifying fibroma

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