Specific code 2006 ICD-9-CM Diagnosis Code 710.1
Systemic sclerosis
  • ICD-9-CM 710.1 will be replaced by an equivalent ICD-10-CM code (or codes) when the United States transitions from ICD-9-CM to ICD-10-CM on October 1, 2015.
  • ICD-9-CM 710.1 is a billable medical code that can be used to specify a diagnosis on a reimbursement claim.
  • You are viewing the 2006 version of ICD-9-CM 710.1.
  • More recent version(s) of ICD-9-CM 710.1: 2007 2008 2009 2010 2011 2012 2013 2014.
Disease Synonyms
  • Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome (disorder)
  • Crest syndrome
  • Lipodermatosclerosis
  • Lung disease with systemic sclerosis
  • Myopathy due to scleroderma (disorder)
  • Myopathy due to systemic sclerosis
  • Polyneuropathy due to systemic sclerosis
  • Progressive systemic sclerosis
  • Scleredema
  • Scleredema buschkes
  • Scleroderma
  • Scleroderma of lung
  • Scleroderma w glomerulonephritis
  • Scleroderma with glomerulonephritis
  • Scleroderma with glomerulonephritis (gn)
  • Systemic sclerosis induced by chemical, including drug
  • Systemic sclerosis induced by chemical, including drugs
  • Systemic sclerosis induced by drugs and chemicals
  • Systemic sclerosis w myopathy
  • Systemic sclerosis w polyneuropathy
710.1 Excludes
  • circumscribed scleroderma (701.0)
Applies To
  • Acrosclerosis
  • CRST syndrome
  • Progressive systemic sclerosis
  • Scleroderma
Use Additional
  • Use additional code to identify manifestation, as:
Convert to ICD-10-CM: 710.1 converts approximately to:
  • 2014 ICD-10-CM M34.0 Progressive systemic sclerosis
    Or:
  • 2014 ICD-10-CM M34.1 CR(E)ST syndrome
    Or:
  • 2014 ICD-10-CM M34.9 Systemic sclerosis, unspecified
ICD-9-CM Volume 2 Index entries containing back-references to 710.1:
  • Acroscleriasis (see also Scleroderma) 710.1
  • Acroscleroderma (see also Scleroderma) 710.1
  • Acrosclerosis (see also Scleroderma) 710.1
  • Buschke's disease or scleredema (adultorum) 710.1
  • Calcinosis (generalized) (interstitial) (tumoral) (universalis) 275.49
    • Raynaud's phenomenonsclerodactylytelangiectasis (CRST) 710.1
  • Chorionitis (see also Scleroderma) 710.1
  • CRST syndrome (cutaneous systemic sclerosis) 710.1
  • Dermatosclerosis (see also Scleroderma) 710.1
  • Disease, diseased - see also Syndrome
    • Buschke's 710.1
  • Scleredema
    • adultorum 710.1
    • Buschke's 710.1
  • Sclerema
    • adultorum 710.1
  • Scleroderma, sclerodermia (acrosclerotic) (diffuse) (generalized) (progressive) (pulmonary) 710.1
  • Sclerosis, sclerotic
    • progressive systemic 710.1
    • systemic (progressive) 710.1
      • with lung involvement 710.1 [517.2]
  • Syndrome - see also Disease
    • CRST (cutaneous systemic sclerosis) 710.1
    • Thibierge-Weissenbach (cutaneous systemic sclerosis) 710.1
    • Weissenbach-Thibierge (cutaneous systemic sclerosis) 710.1
  • Thibierge-Weissenbach syndrome (cutaneous systemic sclerosis) 710.1
  • Trophoneurosis NEC 356.9
    • disseminated 710.1
  • Weissenbach-Thibierge syndrome (cutaneous systemic sclerosis) 710.1
ICD-9-CM codes are used in medical billing and coding to describe diseases, injuries, symptoms and conditions. ICD-9-CM 710.1 is one of thousands of ICD-9-CM codes used in healthcare. Although ICD-9-CM and CPT codes are largely numeric, they differ in that CPT codes describe medical procedures and services. Can't find a code? Start at the root of ICD-9-CM, check the 2006 ICD-9-CM Index or use the search engine at the top of this page to lookup any code.