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 ×

Mucopolysaccharidosis type 7

Beta-glucuronidase deficiency · MPS7

ORPHA:584

Mucopolysaccharidosis type 2

Hunter syndrome · Iduronate 2-sulfatase deficiency

ORPHA:580

Mucopolysaccharidosis type 3

MPS3 · MPSIII

ORPHA:581

Mucopolysaccharidosis type 6

ARSB deficiency · ASB deficiency

ORPHA:583