Version 2024

2024 ICD-10-CM Diagnosis Code M33.1

Other dermatomyositis

ICD-10-CM Code:
M33.1
ICD-10 Code for:
Other dermatomyositis
Is Billable?
Not Valid for Submission
Code Navigator:

Code Classification

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

M33.1 is a non-specific and non-billable diagnosis code code, consider using a code with a higher level of specificity for a diagnosis of other dermatomyositis. The code is not specific and is NOT valid for the year 2024 for the submission of HIPAA-covered transactions. Category or Header define the heading of a category of codes that may be further subdivided by the use of 4th, 5th, 6th or 7th characters.

Specific Coding Applicable to Other dermatomyositis

Non-specific codes like M33.1 require more digits to indicate the appropriate level of specificity. Consider using any of the following ICD-10-CM codes with a higher level of specificity when coding for other dermatomyositis:

  • Use M33.10 for Other dermatomyositis, organ involvement unspecified - BILLABLE CODE

  • Use M33.11 for Other dermatomyositis with respiratory involvement - BILLABLE CODE

  • Use M33.12 for Other dermatomyositis with myopathy - BILLABLE CODE

  • Use M33.13 for Other dermatomyositis without myopathy - BILLABLE CODE

  • Use M33.19 for Other dermatomyositis with other organ involvement - BILLABLE CODE

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)
  • Adult Dermatomyositis

    dermatomyositis in an adult.
  • Childhood Dermatomyositis|JDM|JDM|Juvenile Dermatomyositis|Juvenile Dermatomyositis

    an inflammatory myopathy of childhood resulting in muscle weakness, and associated with a characteristic skin rash.
  • Cutaneous Dermatomyositis Disease Area and Severity Index|CDASI|CDASI

    an instrument that measures activity and damage in the skin of dermatomyositis patients.
  • Dermatomyositis

    inflammation of the skin and muscle.
  • Dermatomyositis Skin Severity Index|DSSI|DSSI

    an assessment of disease activity in the skin of patients with dermatomyositis.
  • Interferon-Induced Helicase C Domain-Containing Protein 1|CADM-140 Autoantigen|Clinically Amyopathic Dermatomyositis Autoantigen 140 kDa|EC 3.6.4.13|Helicard|Helicase with 2 CARD Domains|IFIH1|Interferon-Induced With Helicase C Domain Protein 1|MDA-5|Melanoma Differentiation Associated Protein-5|Melanoma Differentiation-Associated Protein 5|Murabutide Down-Regulated Protein|RLR-2|RNA Helicase-DEAD Box Protein 116

    interferon-induced helicase c domain-containing protein 1 (1025 aa, ~117 kda) is encoded by the human ifih1 gene. this protein is involved in the positive regulation of antiviral responses.
  • Juvenile Dermatomyositis Sine Myositis|Juvenile Amyopathic Dermatomyositis|Juvenile Amyopathic Dermatomyositis|Juvenile Dermatomyositis sine Myositis|Juvenile dermatomyositis without myopathy

    a rare form of juvenile dermatomyositis that manifests with characteristic cutaneous findings for at least six months in the absence of any detectable muscle involvement.
  • Juvenile Dermatomyositis with Myopathy|Juvenile dermatomyositis with myopathy

    evidence of juvenile dermatomyositis with myopathy.
  • Juvenile Dermatomyositis with Other Organ Involvement|Juvenile dermatomyositis with other organ involvement

    evidence of juvenile dermatomyositis with other organ involvement.
  • Juvenile Dermatomyositis with Respiratory Involvement|Juvenile dermatomyositis with respiratory involvement

    evidence of juvenile dermatomyositis with respiratory involvement.
  • Juvenile Dermatomyositis, Organ Involvement Unspecified|Juvenile dermatomyositis, organ involvement unspecified

    evidence of juvenile dermatomyositis, organ involvement unspecified.
  • Other Dermatomyositis with Myopathy|Other dermatomyositis with myopathy

    evidence of other dermatomyositis with myopathy not specified elsewhere.
  • Other Dermatomyositis with Other Organ Involvement|Other dermatomyositis with other organ involvement

    evidence of other dermatomyositis with other organ involvement not specified elsewhere.
  • Other Dermatomyositis with Respiratory Involvement|Other dermatomyositis with respiratory involvement

    evidence of other dermatomyositis with respiratory involvement not specified elsewhere.
  • Other Dermatomyositis without Myopathy|Other dermatomyositis without myopathy

    evidence of other dermatomyositis without myopathy not specified elsewhere.
  • Other Dermatomyositis, Organ Involvement Unspecified|Other dermatomyositis, organ involvement unspecified

    evidence of other dermatomyositis, organ involvement unspecified not specified elsewhere.

Tabular List of Diseases and Injuries

The following annotation back-references are applicable to this diagnosis code. The Tabular List of Diseases and Injuries is a list of ICD-10-CM codes, organized "head to toe" into chapters and sections with coding notes and guidance for inclusions, exclusions, descriptions and more.


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

Patient Education


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


[Learn More in MedlinePlus]

Code History

  • FY 2024 - No Change, effective from 10/1/2023 through 9/30/2024
  • FY 2023 - No Change, effective from 10/1/2022 through 9/30/2023
  • FY 2022 - No Change, effective from 10/1/2021 through 9/30/2022
  • FY 2021 - No Change, effective from 10/1/2020 through 9/30/2021
  • FY 2020 - No Change, effective from 10/1/2019 through 9/30/2020
  • FY 2019 - No Change, effective from 10/1/2018 through 9/30/2019
  • FY 2018 - No Change, effective from 10/1/2017 through 9/30/2018
  • FY 2017 - No Change, effective from 10/1/2016 through 9/30/2017
  • FY 2016 - New Code, effective from 10/1/2015 through 9/30/2016. This was the first year ICD-10-CM was implemented into the HIPAA code set.