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 systemic sclerosis

OBSOLETE: Pediatric systemic scleroderma

ORPHA:93567

Diffuse cutaneous systemic sclerosis

Diffuse cutaneous systemic scleroderma · Progressive cutaneous systemic scleroderma

ORPHA:220393

Limited cutaneous systemic sclerosis

Limited cutaneous systemic scleroderma · Progressive systemic sclerosis

ORPHA:220402

Limited systemic sclerosis

Progressive systemic sclerosis · Scleroderma

ORPHA:220407

OBSOLETE: Pediatric polyarteritis nodosa

OBSOLETE: PAN, pediatric onset

ORPHA:93564

OBSOLETE: Pediatric Sjögren syndrome

ORPHA:93566

Rare pediatric systemic disease

ORPHA:280373

Systemic sclerosis

Progressive systemic sclerosis · Scleroderma

ORPHA:90291