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"

2 matching diseasesClear search ×

Sialidosis type 2

Infantile dysmorphic sialidosis

ORPHA:87876

Sialidosis type 1

Cherry-red spot-myoclonus syndrome · Lipomucopolysaccharidosis

ORPHA:812