M61.179
ICD-10-CMThis code represents a rare, severe genetic disorder characterized by progressive heterotopic ossification (bone formation in soft tissues) affecting the unspecified toe(s). The condition leads to debilitating stiffness and loss of mobility as muscle and connective tissues are gradually replaced by bone.
Apply this code when documentation explicitly states a diagnosis of myositis ossificans progressiva affecting an unspecified toe or toes. This diagnosis is typically made based on clinical presentation, genetic testing, and imaging studies confirming heterotopic ossification.
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