773.2
ICD-9-CMThis code signifies a condition where the red blood cells of a fetus or newborn are destroyed by antibodies from the mother, caused by an incompatibility in blood types other than Rh factor. This isoimmunization leads to anemia and other complications in the infant.
Apply this code when documentation specifies hemolytic disease in a neonate or fetus due to blood group incompatibilities such as ABO, Kell, Duffy, or other minor blood groups. This diagnosis is typically made based on serological testing of maternal and fetal/neonatal blood.
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