M60.031 is the authoritative medical code for Infective myositis, right forearm. This classification is used in medical billing and clinical recording to specify the clinical criteria for infective myositis, right forearm (ICD-10-CM M60.031), ensuring healthcare documentation aligns with current federal coding standards.
Billing Status: YES. This is a valid, specific, and billable ICD-10-CM reference.
Official Registry Overview & Definition
Infective myositis, right forearm is a billable ICD-10-CM diagnosis code M60.031. Excludes1 (not coded here): dermatopolymyositis M33.-; myopathy in amyloidosis E85.-; myopathy in polyarteritis nodosa M30.0; myopathy in rheumatoid arthritis M05.32; myopathy in scleroderma M34.-; myopathy in Sjögren's syndrome M35.03; myopathy in systemic lupus erythematosus M32.-. Excludes2 (not included here): inclusion body myositis IBM; muscular dystrophies and myopathies G71-G72. Use additional code: code B95-B97 to identify infectious agent.
Official Tabular Instructional Notes
Sequencing, inclusion, and exclusion notes published for M60.031 in the official ICD-10-CM tabular list.
Excludes1 — Not Coded Here
Conditions that can never be reported with this code; the two are mutually exclusive.
- dermatopolymyositis M33.-
- myopathy in amyloidosis E85.-
- myopathy in polyarteritis nodosa M30.0
- myopathy in rheumatoid arthritis M05.32
- myopathy in scleroderma M34.-
- myopathy in Sjögren's syndrome M35.03
- myopathy in systemic lupus erythematosus M32.-
Excludes2 — Not Included Here
Conditions not covered by this code, but which may be reported alongside it when both are present.
- inclusion body myositis IBM
- muscular dystrophies and myopathies G71-G72
Use Additional Code
Supplementary codes the tabular list directs you to add.
- code B95-B97 to identify infectious agent
Frequently Asked Questions (FAQ) & Clinical Guidance
What can't be coded together with M60.031?
Per official ICD-10-CM Excludes1 instructions, M60.031 must not be reported together with: dermatopolymyositis (M33.-); myopathy in amyloidosis (E85.-); myopathy in polyarteritis nodosa (M30.0); myopathy in rheumatoid arthritis (M05.32).
Can M60.031 be reported alongside related conditions?
Per official ICD-10-CM Excludes2 instructions, M60.031 and the following are not considered part of each other and may both be reported when both conditions are present: inclusion body myositis [IBM] (G72.41); muscular dystrophies and myopathies (G71-G72).
Is an additional code needed with M60.031?
Use additional code(s) to specify: code (B95-B97) to identify infectious agent.
Nearest Codes in This Family
Official ICD-10-CM classifications closest to M60.031 in its code family, with their registry titles.
- M60.02 — Infective myositis, upper arm
- M60.021 — Infective myositis, right upper arm
- M60.022 — Infective myositis, left upper arm
- M60.029 — Infective myositis, unspecified upper arm
- M60.03 — Infective myositis, forearm
- M60.032 — Infective myositis, left forearm
- M60.039 — Infective myositis, unspecified forearm
- M60.04 — Infective myositis, hand and fingers
- M60.041 — Infective myositis, right hand
- M60.042 — Infective myositis, left hand
View all 40 codes in the M60 family