Polyarteritis with lung involvement [Churg-Strauss]
Billable / specificHCC V28 278
M30.1 is a billable, specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes in FY2027.
Inclusion terms
Applicable to
- Allergic granulomatous angiitis
- Eosinophilic granulomatosis with polyangiitis [EGPA]
Includes (from M30)
- autoimmune disease NOS
- collagen (vascular) disease NOS
- systemic autoimmune disease
- systemic collagen (vascular) disease
- Note: Use an external cause code following the code for the musculoskeletal condition, if applicable, to identify the cause of the musculoskeletal condition
Excludes1
Not coded here — never report together with this code.
Excludes2
Not included here — may be reported together when both conditions exist.
- arthropathic psoriasis (L40.5-) (from M30)
- certain conditions originating in the perinatal period (P04-P96) (from M30)
- certain infectious and parasitic diseases (A00-B99) (from M30)
- compartment syndrome (traumatic) (T79.A-) (from M30)
- complications of pregnancy, childbirth and the puerperium (O00-O9A) (from M30)
- congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99) (from M30)
- endocrine, nutritional and metabolic diseases (E00-E88) (from M30)
- injury, poisoning and certain other consequences of external causes (S00-T88) (from M30)
- neoplasms (C00-D49) (from M30)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94) (from M30)
Also known as
- Allergic granulomatous angiitis
- Eosinophilic granulomatosis with polyangiitis [EGPA]
- Angiitis, allergic granulomatous
- Churg-Strauss syndrome
- EGPA
- Granulomatosis, eosinophilic, with polyangiitis [EGPA]
- Polyarteritis, nodosa, with lung involvement
- Syndrome, Churg-Strauss
Parent code
- M30Polyarteritis nodosa and related conditionsHeader