M60.14 is the authoritative medical code for Interstitial myositis, hand. This classification is used in medical billing and clinical recording to specify the clinical criteria for interstitial myositis, hand (ICD-10-CM M60.14), ensuring healthcare documentation aligns with 2026 federal coding standards.
Billing Status: NO. This is a clinician non-billable / parent hierarchy grouping in the ICD-10-CM system.
Sequencing, inclusion, and exclusion notes published for M60.14 in the official ICD-10-CM tabular list.
Conditions that can never be reported with this code; the two are mutually exclusive.
Conditions not covered by this code, but which may be reported alongside it when both are present.
No. M60.14 (Interstitial myositis, hand) is a non-billable ICD-10-CM category code. A more specific billable subcode must be selected based on clinical documentation.
Per official ICD-10-CM Excludes1 instructions, M60.14 must not be reported together with: dermatopolymyositis (M33.-); myopathy in amyloidosis (E85.-); myopathy in polyarteritis nodosa (M30.0); myopathy in rheumatoid arthritis (M05.32).
Per official ICD-10-CM Excludes2 instructions, M60.14 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).
Official ICD-10-CM classifications closest to M60.14 in its code family, with their registry titles.