M61.139
ICD-10-CMThis code represents a rare, progressive genetic disorder characterized by the abnormal formation of bone in muscles, tendons, ligaments, and other connective tissues, specifically affecting an unspecified forearm. This heterotopic ossification leads to stiffness, pain, and significant functional impairment as the soft tissues gradually turn into bone.
Use this code when documentation confirms a diagnosis of myositis ossificans progressiva (fibrodysplasia ossificans progressiva) affecting an unspecified forearm. This diagnosis is typically made based on clinical presentation, genetic testing, and imaging studies showing heterotopic bone formation.
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