Short answer · Medically reviewed summary · Last updated: 2026-05-08
Churg Strauss Syndrome, now clinically known as Eosinophilic Granulomatosis with Polyangiitis (EGPA), is classified under the ICD-10 code M30.1 (Polyarteritis with lung involvement). In the older ICD-9 coding system, this condition was identified by the code 446.4. What exactly is Churg Strauss Syndrome? Churg Strauss Syndrome is a rare systemic necrotizing vasculitis characterized by asthma, peripheral blood eosinophilia, and inflammation of the blood vessels.
Churg Strauss Syndrome, now clinically known as Eosinophilic Granulomatosis with Polyangiitis (EGPA), is classified under the ICD-10 code M30.1 (Polyarteritis with lung involvement). In the older ICD-9 coding system, this condition was identified by the code 446.4.
Churg Strauss Syndrome is a rare systemic necrotizing vasculitis characterized by asthma, peripheral blood eosinophilia, and inflammation of the blood vessels. Because Churg Strauss Syndrome affects multiple organ systems, including the lungs, skin, nerves, and heart, accurate coding is essential for insurance documentation and tracking clinical outcomes within the 126-member community at DiseaseMaps.org.
While many patients still use the term Churg Strauss Syndrome, the medical community adopted the name Eosinophilic Granulomatosis with Polyangiitis (EGPA) to better reflect the underlying pathology of the disease. Despite this change in nomenclature, the ICD-10 code M30.1 remains the standard identifier for Churg Strauss Syndrome in clinical and administrative settings worldwide.
Medical coding for Churg Strauss Syndrome typically involves the following considerations:
Medical disclaimer: This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment; always consult with a qualified healthcare provider regarding your specific health needs.