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"

3 matching diseasesClear search ×

Congenital infiltrating lipomatosis of the face

CIL-F · Facial infused lipomatosis

ORPHA:583097

Familial angiolipomatosis

ORPHA:199279

Familial multiple lipomatosis

ORPHA:199276