Specific code icon 2017 ICD-10-CM Diagnosis Code M35.1

Other overlap syndromes

    2016 2017 Billable/Specific Code

  • M35.1 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
  • This is the American ICD-10-CM version of M35.1. Other international versions of ICD-10 M35.1 may differ.
  • Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.

Clinical Information
  • A syndrome with overlapping clinical features of systemic lupus erythematosus, scleroderma, polymyositis, and raynaud's phenomenon. The disease is differentially characterized by high serum titers of antibodies to ribonuclease-sensitive extractable (saline soluble) nuclear antigen and a "speckled" epidermal nuclear staining pattern on direct immunofluorescence.
  • An autoimmune overlap syndrome characterized by the presence of symptoms of systemic lupus erythematosus, systemic scleroderma, and polymyositis.
Applicable To
  • Mixed connective tissue disease
Type 1 Excludes
  • polyangiitis overlap syndrome (M30.8)
ICD-10-CM M35.1 is grouped within Diagnostic Related Group(s) (MS-DRG v34.0):
  • 545 Connective tissue disorders with mcc
  • 546 Connective tissue disorders with cc
  • 547 Connective tissue disorders without cc/mcc

Convert ICD-10-CM M35.1 to ICD-9-CM

The following ICD-10-CM Index entries contain back-references to ICD-10-CM M35.1: