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 ×

Papular mucinosis of infancy

Cutaneous mucinosis of infancy

ORPHA:90395

Localized lichen myxedematosus

Papular mucinosis

ORPHA:86795

Acral persistent papular mucinosis

ORPHA:90396

Self-healing papular mucinosis

ORPHA:90397