V17.2
ICD-9-CMThis code indicates a patient's family history of neurological conditions not specifically categorized elsewhere. It signifies a genetic predisposition or increased risk for developing various disorders affecting the brain, spinal cord, or peripheral nerves.
Apply this code when documentation indicates a family history of neurological diseases such as multiple sclerosis, Parkinson's disease, Huntington's disease, or other specified but uncoded neurological conditions. It is used to provide context for a patient's current symptoms or for risk assessment during preventative care.
AI-generated reference. Verify against official guidelines.
Code History