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"

9 matching diseasesClear search ×

Scleroderma

ORPHA:801

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

Systemic sclerosis

Progressive systemic sclerosis · Scleroderma

ORPHA:90291

Localized scleroderma

Localized fibrosing scleroderma

ORPHA:90289

Neonatal scleroderma

ORPHA:398127

Scleredema

Buschke scleredema

ORPHA:352763

Scleromyxedema

Arndt-Gottron disease · Generalized lichenoid papular eruption

ORPHA:167635