Genetic susceptibility to malignant neoplasm of ovary

This code signifies an individual's increased genetic predisposition to developing ovarian cancer. It indicates the presence of specific genetic mutations or inherited factors that elevate the lifetime risk of malignancy in the ovaries, even in the absence of current disease.

Apply this code when a patient has a documented genetic mutation (e.g., BRCA1/2) or a strong family history indicating a high inherited risk for ovarian cancer, but no current ovarian malignancy. It is appropriate for risk assessment, genetic counseling, and prophylactic management scenarios.

• Do not use this code if the patient has an active ovarian malignancy; instead, code the specific cancer.
• Ensure documentation clearly states the genetic susceptibility or inherited risk, not just a family history of cancer.
• This code is often used in conjunction with codes for genetic testing or counseling services.