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M30.2

Billable

Juvenile polyarteritis

HCC Category Mapping

V28HCC 94Reactive and Specified Arthropathies
0.000
V24HCC 40Rheumatoid Arthritis and Inflammatory Connective Tissue Disease
0.307
ESRDHCC 40Rheumatoid Arthritis and Inflammatory Connective Tissue Disease
0.000
RxHCCHCC 84Vasculitis and Other Autoimmune Disorders
0.000

What This Code Means

A rare form of polyarteritis nodosa that occurs in children, causing inflammation of medium-sized arteries and potentially affecting multiple organs.

Coding Tips

  • Always verify the patient's age is consistent with juvenile classification
  • Document the specific organs involved and any complications to guide treatment decisions

Clinical Significance

Juvenile polyarteritis is a rare pediatric form of systemic necrotizing vasculitis affecting medium-sized arteries in children. Early recognition and aggressive treatment are crucial to prevent organ damage and optimize long-term outcomes in growing patients.

Documentation Requirements

  • Patient age confirming pediatric population
  • Clinical evidence of medium-vessel necrotizing arteritis
  • Biopsy confirmation or characteristic imaging findings
  • Documentation of systemic manifestations
  • Exclusion of other pediatric vasculitides
  • Assessment of growth and development impact
  • Family history and genetic considerations
  • Long-term monitoring plan for complications

Commonly Confused Codes

Code Hierarchy

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