interstitial lung disease amyopathic dermatomyositis https://github.com/monarch-initiative/mondo/issues/8118 A form of dermatomyositis characterized by the presence of typical skin finding swithout muscle weakness. Some of the skin changes that suggest dermatomyositis include a pink rash on the face, neck, forearms and upper chest; Gottron's papules and heliotrope eyelids. Pruritis and photosensitivity are common, as is scalp inflammation and thinning of the hair.While patients with amyopathic dermatomyositis should not have clinically evident muscle weakness, minor muscle abnormalities may be included.Fatigue is reported in at least 50% of patients. Some cases have beenassociated with internal malignancy and/or interstitial lung disease. Treatment may include sun avoidance, ample use of sunscreen, topical corticosteroids, antimalarial agents, methotrexate, mycophenolate mofetil, or intravenous (IV) immunoglobulin. GARD:0009907 NANDO:1200275 icd11.foundation:727262285 MEDGEN:96065 amyopathic dermatomyositis SCTID:238935002 MESH:C538250 MONDO:0043317 UMLS:C0406645 Orphanet:645617 ADM dermatomyositis sine myositis clinically amyopathic dermatomyositis