Family history of congenital anomalies

This code indicates a patient's family history of birth defects or structural abnormalities present at birth. It signifies that one or more immediate or extended family members have been diagnosed with a congenital anomaly. This history may be relevant for genetic counseling, risk assessment, or guiding diagnostic workups.

Use this code when documenting a patient's family history that includes conditions like spina bifida, heart defects, cleft lip/palate, or other malformations present from birth. This is often recorded during initial patient assessments, prenatal care, or when evaluating a patient for potential genetic predispositions.

• This is a V-code, indicating a factor influencing health status rather than a current disease.
• Always sequence this code after the primary reason for the encounter, if applicable.
• Ensure the medical record clearly documents the specific congenital anomaly and the affected family member(s).