Diseases of the musculoskeletal system and connective tissue
Systemic connective tissue disorders
Other necrotizing vasculopathies
2017/18 ICD-10-CM Diagnosis Code M31.3
2016 2017 2018 Non-Billable/Non-Specific Code
- M31.3 should not be used for reimbursement purposes as there are multiple codes below it that contain a greater level of detail.
- The 2018 edition of ICD-10-CM M31.3 became effective on October 1, 2017.
- This is the American ICD-10-CM version of M31.3 - other international versions of ICD-10 M31.3 may differ.
- Necrotizing respiratory granulomatosis
The following code(s) above M31.3
contain annotation back-references
In this context, annotation back-references refer to codes that contain:
- Applicable To annotations, or
- Code Also annotations, or
- Code First annotations, or
- Excludes1 annotations, or
- Excludes2 annotations, or
- Includes annotations, or
- Note annotations, or
- Use Additional annotations
that may be applicable to M31.3
- A multisystemic disease of a complex genetic background. It is characterized by inflammation of the blood vessels (vasculitis) leading to damage in any number of organs. The common features include granulomatous inflammation of the respiratory tract and kidneys. Most patients have measurable autoantibodies (antineutrophil cytoplasmic antibodies) against neutrophil proteinase-3 (wegener autoantigen).
- A rare, autoimmune, systemic medium and small size vasculitis. It is characterized by the formation of necrotizing granulomas in the respiratory tract, necrotizing angiitis, and glomerulonephritis.
- Multisystem disease chiefly affecting males, characterized by necrotizing granulomatous vasculitis involving the upper and lower respiratory tracts, glomerulonephritis, and variable degrees of systemic small vessel vasculitis; considered an aberrant hypersensitivity reaction to an unknown antigen.
- Wegener's granulomatosis is a rare disease. It is a type of vasculitis, or inflammation of the blood vessels. The inflammation limits the flow of blood to important organs, causing damage. It can affect any organ, but it mainly affects the sinuses, nose, trachea (windpipe), lungs, and kidneys. The cause of wegener's granulomatosis is unknown. It can affect people at any age. Men and women are equally affected. It is more common in whites. Symptoms may include joint pain, weakness, tiredness, and cold symptoms such as a runny nose that doesn't get better. Doctors use blood tests, chest x-rays, and biopsies to diagnose the disease and rule out other causes of the symptoms.early treatment is important. Most people improve with medicines to slow or stop the inflammation.
- 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
- 2017 (effective 10/1/2016): No change
- 2018 (effective 10/1/2017): No change
Code annotations containing back-references to M31.3:
ICD-10-CM Codes Adjacent To M31.3
Polyarteritis nodosa and related conditions
Polyarteritis with lung involvement [Churg-Strauss]
Mucocutaneous lymph node syndrome [Kawasaki]
Other conditions related to polyarteritis nodosa
Other necrotizing vasculopathies
Lethal midline granuloma
…… without renal involvement
…… with renal involvement
Aortic arch syndrome [Takayasu]
Giant cell arteritis with polymyalgia rheumatica
Other giant cell arteritis
Other specified necrotizing vasculopathies
Necrotizing vasculopathy, unspecified
Systemic lupus erythematosus (SLE)
Drug-induced systemic lupus erythematosus
Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.