Rare Zebra

Rare disease search prototype built on Orphanet data

← Back to search

ORPHA:221

Dermatomyositis

Also called Adult dermatomyositis

Body system
Skin diseases
Inheritance pattern
Not applicable
Typical age of onset
Adult, Elderly
Estimated prevalence
1-9 / 1 000 000 (Australia)
Rarity class
1-9 / 1 000 000

ORPHA:221 is classified under "Skin diseases" in the Orphanet nomenclature.

Common signs

  • Edema
  • Autoimmunity
  • Limb-girdle muscle weakness
  • Myalgia
  • Proximal muscle weakness
  • Inflammatory myopathy