ORPHA:90291
Systemic sclerosis
Also called Systemic scleroderma
- Body system
- Skin diseases
- Inheritance pattern
- Multigenic/multifactorial, Not applicable
- Typical age of onset
- Adult
- Estimated prevalence
- 1-5 / 10 000 (Europe)
- Rarity class
- 1-5 / 10 000
ORPHA:90291 is classified under "Skin diseases" in the Orphanet nomenclature.
Common signs
- Thickened skin
- Arthralgia
- Myalgia
- Antinuclear antibody positivity
- Abnormality of the gastrointestinal tract
- Raynaud phenomenon