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 ×

Papular mucinosis of infancy

Cutaneous mucinosis of infancy

ORPHA:90395

Cutaneous mastocytosis

ORPHA:66646

Cutaneous myiasis

ORPHA:99983