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 ×

Lysosomal storage disease with skeletal involvement

Dysostosis multiplex

ORPHA:93448

Dysostosis

ORPHA:364559

Maxillonasal dysplasia

Binder syndrome · Maxillonasal dysostosis

ORPHA:1248

Patellar dysostosis

ORPHA:93455