ORPHA:779
Reynolds syndrome
Also called Primary biliary cirrhosis and systemic scleroderma
- Body system
- Skin diseases
- Inheritance pattern
- Not applicable
- Typical age of onset
- Adult
- Estimated prevalence
- Unknown (Worldwide)
- Rarity class
- Unknown
ORPHA:779 is classified under "Skin diseases" in the Orphanet nomenclature.
Common signs
- Pruritus
- Gastroesophageal reflux
- Hepatomegaly
- Myalgia
- Abnormality of the gastric mucosa
- Generalized abnormality of skin