Family history of endo, nutritional and metabolic diseases

This code indicates a documented family history of endocrine, nutritional, or metabolic disorders other than diabetes mellitus, thyroid disease, or cystic fibrosis. It signifies a genetic predisposition or increased risk for these conditions within the patient's immediate or extended family.

Apply this code when a patient's family history includes conditions like familial hypercholesterolemia, hereditary hemochromatosis, or specific genetic metabolic disorders. It is used to explain the rationale for screening, monitoring, or genetic counseling in patients who may be at higher risk due to their family background.

• Always sequence this code as a secondary diagnosis, as it describes a risk factor, not a current condition.
• Ensure the medical record clearly documents the specific "other" endocrine, nutritional, or metabolic disease in the family history.
• Do not use this code if a more specific family history code (e.g., for diabetes or thyroid disease) is available.