V16.8
ICD-9-CMThis code indicates a patient's family history of a malignant neoplasm that is not specifically classified elsewhere in the ICD-9-CM system. It signifies a genetic predisposition or increased risk for a type of cancer that doesn't have a more precise family history code.
Use this code when a patient reports a family history of a malignant neoplasm, and the specific type of cancer is known but does not have a dedicated family history code (e.g., family history of adrenal carcinoma, pancreatic neuroendocrine tumor). It is appropriate when the family history is relevant to the patient's current risk assessment or management.
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