M61.162
ICD-10-CMThis code describes a rare, severe genetic disorder characterized by progressive heterotopic ossification (bone formation in soft tissues) specifically affecting the left lower leg. This condition leads to debilitating stiffness and immobility as muscle, tendons, and ligaments gradually transform into bone.
Use this code when documentation confirms a diagnosis of myositis ossificans progressiva with the primary site of involvement being the left lower leg. This diagnosis is typically made based on clinical presentation, genetic testing (ACVR1 mutation), and imaging studies showing heterotopic bone formation.
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