Rare Disease Library

Browse Orphanet-curated rare diseases with HPO phenotype annotations, synonyms, and linked support programs. Search by name, abbreviation, or synonym.

Try: "IgA nephropathy", "C3G", "Berger's disease", "PKU", "Duchenne"

4 matching diseasesClear search ×

Familial ossifying fibroma

Multiple ossifying fibroma · Familial Gigantiform cementoma

ORPHA:435329

Familial multiple discoid fibromas

Familial multiple trichodiscomas

ORPHA:538756

Familial multiple fibrofolliculoma

ORPHA:338

Multiple non-ossifying fibromatosis

Jaffe-Campanacci syndrome

ORPHA:2029