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"

10 matching diseasesClear search ×

Systemic sclerosis

Progressive systemic sclerosis · Scleroderma

ORPHA:90291

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

Localized scleroderma

Localized fibrosing scleroderma

ORPHA:90289

Neonatal scleroderma

ORPHA:398127

OBSOLETE: Pediatric systemic sclerosis

OBSOLETE: Pediatric systemic scleroderma

ORPHA:93567

Reynolds syndrome

Primary biliary cirrhosis and systemic scleroderma

ORPHA:779

Scleroderma

ORPHA:801

Systemic polyarteritis nodosa

Systemic PAN · Systemic periarteritis nodosa

ORPHA:439762