Z84.89
ICD-10-CMThis code indicates a documented family history of a medical condition that is not specifically categorized elsewhere in the Z80-Z84 range. It signifies a genetic predisposition or increased risk for a particular disease or disorder within a patient's biological family. This information is crucial for risk assessment and preventive care planning.
Apply this code when a patient reports a family history of a specific condition for which a more precise family history code (e.g., Z80 for malignant neoplasm, Z81 for mental and behavioral disorders) does not exist. Examples include family history of specific autoimmune diseases, rare genetic disorders, or certain congenital anomalies not covered by other Z codes.
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