2013 ICD-9-CM Diagnosis Code 710.1
Systemic sclerosis
- chronic hardening and thickening of the skin caused by swelling and thickening of fibrous tissue leading to eventual atrophy of the epidermis; can occur as a localized or a systemic disease.
- A chronic disorder marked by hardening and thickening of the skin. Scleroderma can be localized or it can affect the entire body (systemic).
- systemic disorder of the connective tissue; manifested by hardening and thickening of the skin, by abnormalities involving the microvasculature and larger vessels, and by fibrotic degenerative changes in various body organs including the heart, lungs, kidneys, and gastrointestinal tract.
- A chronic disorder, possibly autoimmune, marked by excessive production of collagen which results in hardening and thickening of body tissues. The two types of systemic scleroderma, limited cutaneous and diffuse cutaneous are classified with focus on the extent of affected skin. A relationship exists between the extent of skin area affected and degree of internal organ/system involvement. Systemic scleroderma can manifest itself in pulmonary fibrosis, Raynaud's syndrome, digestive system telangiectasias, renal hypertension and/or pulmonary hypertension.
- ICD-9-CM 710.1 is a billable medical code that can be used to specify a diagnosis on a reimbursement claim.
710.1 Alternative Terminology
710.1 Excludes 
)Applies To
Use Additional
Convert 710.1 to ICD-10-CM
ICD-9-CM Volume 2 Index entries containing back-references to 710.1:
Raynaud's phenomenonsclerodactylytelangiectasis (CRST) 
adultorum 
