V18.2
ICD-9-CMThis code indicates a patient's personal history of a family member (e.g., parent, sibling, child) having been diagnosed with anemia. It signifies a genetic predisposition or familial pattern of anemia, rather than the patient currently suffering from the condition. This information is crucial for assessing risk and guiding preventive or diagnostic strategies.
Use this code when documentation explicitly states a family history of anemia, even if the specific type of anemia is not detailed. It is appropriate for patients undergoing routine physicals, risk assessments, or when a clinician is investigating potential hereditary factors contributing to a patient's symptoms or conditions.
AI-generated reference. Verify against official guidelines.
Code History