Polyarteritis nodosa and related conditions (M30)
The ICD-10 code M30 covers polyarteritis nodosa and related conditions, a group of disorders involving inflammation of medium-sized arteries throughout the body. These codes are used to classify different forms and manifestations of this systemic vasculitis, including variants affecting lungs, children, and mucocutaneous tissues.
The main code, M30.0, represents polyarteritis nodosa itself, which is sometimes also called primary systemic arteritis or vasculitis of medium sized vessels. This code helps identify cases where arteries become inflamed causing diverse symptoms like neuropathy, myopathy, or nephrotic syndrome. When lung involvement occurs, M30.1 is applied; this includes conditions such as Churg-Strauss syndrome or eosinophilic granulomatosis with polyangiitis. The pediatric form, known as juvenile polyarteritis, is captured by M30.2. M30.3 covers Kawasaki disease, a mucocutaneous lymph node syndrome linked to inflammation of coronary arteries and aneurysm risk. Other related necrotizing vasculitis types fall under M30.8. These precise ICD-10 codes provide essential tools for medical coders to document specific types of polyarteritis nodosa and its variants for accurate diagnosis, treatment, and statistical tracking.
Diseases of the musculoskeletal system and connective tissue (M00–M99)
Systemic connective tissue disorders (M30-M36)
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
Polyarteritis nodosa and related conditions (M30)
Instructional Notations
Type 1 Excludes
A type 1 excludes note is a pure excludes note. It means "NOT CODED HERE!" An Excludes1 note indicates that the code excluded should never be used at the same time as the code above the Excludes1 note. An Excludes1 is used when two conditions cannot occur together, such as a congenital form versus an acquired form of the same condition.
- microscopic polyarteritis M31.7
Clinical Terms
The following clinical terms provide additional context, helping users better understand the clinical background and common associations for each diagnosis listed in this section. Including related terms alongside ICD-10-CM codes supports coders, billers, and healthcare professionals in improving accuracy, enhancing documentation, and facilitating research or patient education.
Mucocutaneous Lymph Node Syndrome
An acute, febrile, mucocutaneous condition accompanied by swelling of cervical lymph nodes in infants and young children. The principal symptoms are fever, congestion of the ocular conjunctivae, reddening of the lips and oral cavity, protuberance of tongue papillae, and edema or erythema of the extremities.
Polyarteritis Nodosa
A form of necrotizing non-granulomatous inflammation occurring primarily in medium-sized ARTERIES, often with microaneurysms. It is characterized by muscle, joint, and abdominal pain resulting from arterial infarction and scarring in affected organs. Polyarteritis nodosa with lung involvement is called CHURG-STRAUSS SYNDROME.