ICD-10-CM Code M33.1

Other dermatomyositis

Version 2020 Non-Billable Code

Not Valid for Submission

M33.1 is a "header" nonspecific and non-billable code code, consider using a code with a higher level of specificity for a diagnosis of other dermatomyositis. The code is NOT valid for the year 2020 for the submission of HIPAA-covered transactions.

ICD-10:M33.1
Short Description:Other dermatomyositis
Long Description:Other dermatomyositis

Consider the following ICD-10 codes with a higher level of specificity:

  • M33.10 - ... organ involvement unspecified
  • M33.11 - Other dermatomyositis with respiratory involvement
  • M33.12 - Other dermatomyositis with myopathy
  • M33.13 - Other dermatomyositis without myopathy
  • M33.19 - Other dermatomyositis with other organ involvement

Tabular List of Diseases and Injuries

The Tabular List of Diseases and Injuries is a list of ICD-10 codes, organized "head to toe" into chapters and sections with guidance for inclusions, exclusions, descriptions and more. The following references are applicable to the code M33.1:

Inclusion Terms

Inclusion Terms
These terms are the conditions for which that code is to be used. The terms may be synonyms of the code title, or, in the case of "other specified" codes, the terms are a list of the various conditions assigned to that code. The inclusion terms are not necessarily exhaustive. Additional terms found only in the Alphabetic Index may also be assigned to a code.
  • Adult dermatomyositis

Clinical Information

  • DERMATOMYOSITIS-. a subacute or chronic inflammatory disease of muscle and skin marked by proximal muscle weakness and a characteristic skin rash. the illness occurs with approximately equal frequency in children and adults. the skin lesions usually take the form of a purplish rash or less often an exfoliative dermatitis involving the nose cheeks forehead upper trunk and arms. the disease is associated with a complement mediated intramuscular microangiopathy leading to loss of capillaries muscle ischemia muscle fiber necrosis and perifascicular atrophy. the childhood form of this disease tends to evolve into a systemic vasculitis. dermatomyositis may occur in association with malignant neoplasms. from adams et al. principles of neurology 6th ed pp1405 6

Code Classification

  • Diseases of the musculoskeletal system and connective tissue (M00–M99)
    • Systemic connective tissue disorders (M30-M36)
      • Dermatopolymyositis (M33)

Code History

  • FY 2016 - New Code, effective from 10/1/2015 through 9/30/2016
    (First year ICD-10-CM implemented into the HIPAA code set)
  • FY 2017 - No Change, effective from 10/1/2016 through 9/30/2017
  • FY 2018 - No Change, effective from 10/1/2017 through 9/30/2018
  • FY 2019 - No Change, effective from 10/1/2018 through 9/30/2019
  • FY 2020 - No Change, effective from 10/1/2019 through 9/30/2020

Information for Patients


Myositis

Myositis means inflammation of the muscles that you use to move your body. An injury, infection, or autoimmune disease can cause it. Two specific kinds are polymyositis and dermatomyositis. Polymyositis causes muscle weakness, usually in the muscles closest to the trunk of your body. Dermatomyositis causes muscle weakness, plus a skin rash.

Other symptoms of myositis may include

  • Fatigue after walking or standing
  • Tripping or falling
  • Trouble swallowing or breathing

Doctors may use a physical exam, lab tests, imaging tests and a muscle biopsy to diagnose myositis. There is no cure for these diseases, but you can treat the symptoms. Polymyositis and dermatomyositis are first treated with high doses of a corticosteroid. Other options include medications, physical therapy, exercise, heat therapy, assistive devices, and rest.

NIH: National Institute of Neurological Disorders and Stroke


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