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ICD-10-CM Codes
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M00-M99
Diseases of the musculoskeletal system and connective tissue
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M30-M36
Systemic connective tissue disorders
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M30-
Polyarteritis nodosa and related conditions
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2022 ICD-10-CM Diagnosis Code M30.1
2022 ICD-10-CM Diagnosis Code M30.1
Polyarteritis with lung involvement [Churg-Strauss]
2016 2017 2018 2019 2020 2021 2022 Billable/Specific Code
- M30.1 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- The 2022 edition of ICD-10-CM M30.1 became effective on October 1, 2021.
- This is the American ICD-10-CM version of M30.1 - other international versions of ICD-10 M30.1 may differ.
Applicable To- Allergic granulomatous angiitis
- Eosinophilic granulomatosis with polyangiitis [EGPA]
The following code(s) above
M30.1 contain annotation back-references
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
M30.1:
- M00-M99
2022 ICD-10-CM Range M00-M99
Diseases of the musculoskeletal system and connective tissueNote- Use an external cause code following the code for the musculoskeletal condition, if applicable, to identify the cause of the musculoskeletal condition
Type 2 Excludes- 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)
- M30-M36
2022 ICD-10-CM Range M30-M36
Systemic connective tissue disordersIncludes- autoimmune disease NOS
- collagen (vascular) disease NOS
- systemic autoimmune disease
- systemic collagen (vascular) disease
Type 1 Excludes- autoimmune disease, single organ or single cell-type -code to relevant condition category
- M30
ICD-10-CM Diagnosis Code M30
Polyarteritis nodosa and related conditions
2016 2017 2018 2019 2020 2021 2022 Non-Billable/Non-Specific Code
Type 1 Excludes- microscopic polyarteritis (M31.7)
- Allergic granulomatosis angiitis
- Churg strauss polyarteritis w pulmonary involvement
- Pulmonary disease due to allergic granulomatosis angiitis
Clinical Information
- An autoimmune necrotizing vasculitis with the formation of granulomas. It is a pulmonary and systemic vasculitis associated with eosinophilia.
- Widespread necrotizing angiitis with granulomas. Pulmonary involvement is frequent. Asthma or other respiratory infection may precede evidence of vasculitis. Eosinophilia and lung involvement differentiate this disease from polyarteritis nodosa.
ICD-10-CM M30.1 is grouped within Diagnostic Related Group(s) (MS-DRG v39.0):
- 542 Pathological fractures and musculoskeletal and connective tissue malignancy with mcc
- 543 Pathological fractures and musculoskeletal and connective tissue malignancy with cc
- 544 Pathological fractures and musculoskeletal and connective tissue malignancy without cc/mcc
Convert M30.1 to ICD-9-CM
Code History
- 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
- 2019 (effective 10/1/2018): No change
- 2020 (effective 10/1/2019): No change
- 2021 (effective 10/1/2020): No change
- 2022 (effective 10/1/2021): No change
Code annotations containing back-references to M30.1:
- Angiitis I77.6
ICD-10-CM Diagnosis Code I77.6
Arteritis, unspecified
2016 2017 2018 2019 2020 2021 2022 Billable/Specific Code
Applicable To- Aortitis NOS
- Endarteritis NOS
- allergic granulomatous M30.1
- Churg-Strauss syndrome M30.1
- EGPA M30.1 (eosinophilic granulomatosis with polyangiitis)
- Granulomatosis L92.9
ICD-10-CM Diagnosis Code L92.9
Granulomatous disorder of the skin and subcutaneous tissue, unspecified
2016 2017 2018 2019 2020 2021 2022 Billable/Specific Code
- eosinophilic, with polyangiitis [EGPA] M30.1
- Polyarteritis
- nodosa M30.0
ICD-10-CM Diagnosis Code M30.0
Polyarteritis nodosa
2016 2017 2018 2019 2020 2021 2022 Billable/Specific Code
- with lung involvement M30.1
- Syndrome - see also Disease
ICD-10-CM Codes Adjacent To M30.1
M27.59 Other periradicular pathology associated with previous endodontic treatment
M27.6 Endosseous dental implant failure
M27.61 Osseointegration failure of dental implant
M27.62 Post-osseointegration biological failure of dental implant
M27.63 Post-osseointegration mechanical failure of dental implant
M27.69 Other endosseous dental implant failure
M27.8 Other specified diseases of jaws
M27.9 Disease of jaws, unspecified
M30 Polyarteritis nodosa and related conditions
M30.0 Polyarteritis nodosa
M30.1
Polyarteritis with lung involvement [Churg-Strauss]
M30.2 Juvenile polyarteritis
M30.3 Mucocutaneous lymph node syndrome [Kawasaki]
M30.8 Other conditions related to polyarteritis nodosa
M31 Other necrotizing vasculopathies
M31.0 Hypersensitivity angiitis
M31.1 Thrombotic microangiopathy
M31.11 Hematopoietic stem cell transplantation-associated thrombotic microangiopathy [HSCT-TMA]
M31.19 Other thrombotic microangiopathy
M31.2 Lethal midline granuloma
Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.
