2027 ICD-10-CM Diagnosis Code M33Dermatopolymyositis
M33 is a non-billable ICD-10-CM category code for dermatopolymyositis, so it cannot be submitted on claims. Use a more specific code from this category instead, such as M33.00, M33.01, M33.02, and M33.03.
Code Identity
Code Classification
Specific Coding for DermatopolymyositisOverview
Non-specific codes like M33 require more characters. Use one of these billable codes instead:
M33.0 for Juvenile dermatomyositis
Use M33.00 for Juvenile dermatomyositis, organ involvement unspecified
Use M33.01 for Juvenile dermatomyositis with respiratory involvement
Use M33.02 for Juvenile dermatomyositis with myopathy
Use M33.03 for Juvenile dermatomyositis without myopathy
Use M33.09 for Juvenile dermatomyositis with other organ involvement
M33.1 for Other dermatomyositis
Use M33.10 for Other dermatomyositis, organ involvement unspecified
Use M33.11 for Other dermatomyositis with respiratory involvement
Use M33.12 for Other dermatomyositis with myopathy
Use M33.13 for Other dermatomyositis without myopathy
Use M33.19 for Other dermatomyositis with other organ involvement
M33.2 for Polymyositis
Use M33.20 for Polymyositis, organ involvement unspecified
Use M33.21 for Polymyositis with respiratory involvement
Use M33.22 for Polymyositis with myopathy
Use M33.29 for Polymyositis with other organ involvement
M33.9 for Dermatopolymyositis, unspecified
Use M33.90 for Dermatopolymyositis, unspecified, organ involvement unspecified
Use M33.91 for Dermatopolymyositis, unspecified with respiratory involvement
Use M33.92 for Dermatopolymyositis, unspecified with myopathy
Use M33.93 for Dermatopolymyositis, unspecified without myopathy
Use M33.99 for Dermatopolymyositis, unspecified with other organ involvement
Instructional NotesGuidance
Instructions from the official ICD-10-CM Tabular List that apply to M33: its own notes plus those printed at block M30-M36 and Chapter 13. A note printed at a category, block or chapter applies to every code under it.
Includes
Further defines, or gives examples of, the content of the category.
- autoimmune disease NOS
- collagen (vascular) disease NOS
- systemic autoimmune disease
- systemic collagen (vascular) disease
Excludes1
Not coded here: the excluded code is never reported together with this one, unless the two conditions are unrelated.
- autoimmune disease, single organ or single cell-type -code to relevant condition category
Excludes2
Not included here: the excluded condition is not part of this code, but a patient may have both, so both codes may be reported.
- arthropathic psoriasis (L40.5-)
- certain conditions originating in the perinatal period (P04-P96)
- certain infectious and parasitic diseases (A00-B99)
- compartment syndrome (traumatic) (T79.A-)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
Notes
General instructions on how these codes are used.
- Use an external cause code following the code for the musculoskeletal condition, if applicable, to identify the cause of the musculoskeletal condition
Source: CMS ICD-10-CM Tabular List. How to read instructional notes.
Referenced in Other NotesGuidance
Instructional notes printed at other codes that name M33, its category, or a range that includes it.
Excludes1 3
These codes carry an Excludes1 note naming M33: they are not reported together with it, unless the two conditions are unrelated.
- G72 Other and unspecified myopathiesdermatopolymyositis (M33.-)
- Block M60-M63 Disorders of musclesdermatopolymyositis (M33.-)
- L94 Other localized connective tissue disorders
Excludes2 4
These codes carry an Excludes2 note naming M33: its condition is not part of those codes, and both may be reported when the patient has both.
- Chapter 9 (I00-I99) Diseases of the circulatory system
- I77 Other disorders of arteries and arterioles
- J82 Pulmonary eosinophilia, not elsewhere classified
- Chapter 12 (L00-L99) Diseases of the skin and subcutaneous tissue
Code First 1
These codes say to code first a condition named in the note, and M33 is one of the conditions named.
- J84.170 Interstitial lung disease with progressive fibrotic phenotype in diseases classified elsewhere
Clinical InformationClinical
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)
Patient EducationClinical
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.
Read the full article at MedlinePlus
Courtesy of MedlinePlus, a service of the U.S. National Library of Medicine.
Code HistoryHistory
Questions About M33Overview
What is the ICD-10 code for dermatopolymyositis?
M33 is the ICD-10-CM category for dermatopolymyositis, but it is a non-billable header: claims need a more specific code from this category, listed on this page.