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"

7 matching diseasesClear search ×

Dubin-Johnson syndrome

Dubin-Sprinz disease · Hyperbilirubinemia type 2

ORPHA:234

Infantile mercury poisoning

Erythroedema polyneuritis · Feer disease

ORPHA:247165

Mucopolysaccharidosis type 7

Beta-glucuronidase deficiency · MPS7

ORPHA:584

Rare skin disease

ORPHA:89826

Salla disease

ORPHA:309334

Systemic-onset juvenile idiopathic arthritis

Still disease · Systemic-onset JIA

ORPHA:85414

X-linked lymphoproliferative disease

Duncan disease · Purtilo syndrome

ORPHA:2442