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"

8 matching diseasesClear search ×

Mazabraud syndrome

Myxoma with fibrous dysplasia

ORPHA:57782

Acute panmyelosis with myelofibrosis

Acute myelodysplasia with myelofibrosis · Acute myelofibrosis

ORPHA:86843

Fibromuscular dysplasia

FMD

ORPHA:698012

Fibrous dysplasia of bone

ORPHA:249

Fibrous dysplasia/McCune-Albright syndrome

Fibrous dysplasia/McCune-Albright spectrum · FD/MAS spectrum

ORPHA:595216

Monostotic fibrous dysplasia

Jaffe-Lichtenstein disease

ORPHA:93277

Osteofibrous dysplasia

OFD

ORPHA:488265

Polyostotic fibrous dysplasia

ORPHA:93276