Z15.89
ICD-10-CMThis code signifies a patient's increased likelihood of developing a specific disease due to inherited genetic factors, where the particular disease is not specified by a more precise genetic susceptibility code. It indicates a predisposition identified through genetic testing or family history, but not yet a current manifestation of the disease itself.
Use this code when a patient has a documented genetic susceptibility to a disease that doesn't have a more specific Z15 code (e.g., Z15.01 for malignant neoplasm of breast). This is appropriate for patients undergoing genetic counseling or surveillance due to a known genetic risk for conditions like certain autoimmune disorders, neurological conditions, or other non-neoplastic diseases.
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