V16.9
ICD-9-CMThis code indicates a patient's family history of cancer where the specific type of malignancy is not documented or is unknown. It signifies a genetic predisposition or increased risk for cancer due to a family history, but without further detail on the primary site or histological type.
This code is appropriate when a patient reports a family history of cancer, but the medical record lacks specific information about the type of cancer. It is often used for screening purposes or when assessing a patient's risk profile for various cancers based on a general family history.
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