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 ×

Limited systemic sclerosis

Progressive systemic sclerosis · Scleroderma

ORPHA:220407

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

OBSOLETE: Pediatric systemic sclerosis

OBSOLETE: Pediatric systemic scleroderma

ORPHA:93567

Reynolds syndrome

Primary biliary cirrhosis and systemic scleroderma

ORPHA:779

Scleroderma

ORPHA:801

Sclerosteosis

Cortical hyperostosis-syndactyly syndrome

ORPHA:3152

Systemic sclerosis

Progressive systemic sclerosis · Scleroderma

ORPHA:90291