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"

8 matching diseasesClear search ×

OBSOLETE: Pediatric polyarteritis nodosa

OBSOLETE: PAN, pediatric onset

ORPHA:93564

OBSOLETE: Hereditary pediatric Behçet-like disease

OBSOLETE: Behçet-like disease due to HA20 · OBSOLETE: Behçet-like disease due to haploinsufficiency of A20

ORPHA:476102

OBSOLETE: Pediatric Castleman disease

ORPHA:93682

OBSOLETE: Pediatric Sjögren syndrome

ORPHA:93566

OBSOLETE: Pediatric systemic sclerosis

OBSOLETE: Pediatric systemic scleroderma

ORPHA:93567

Pediatric systemic lupus erythematosus

Disseminated lupus erythematosus · Lupus

ORPHA:93552

Pediatric-onset glaucoma

ORPHA:523000

Pediatric-onset Graves disease

Pediatric-onset Basedow disease

ORPHA:525731