P55.9

Hemolytic disease of newborn, unspecified

Billable / specificHCC V28 109

P55.9 is a billable, specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes in FY2027.

Inclusion terms

conditions that have their origin in the fetal or perinatal period (before birth through the first 28 days after birth) even if morbidity occurs later
Note: Codes from this chapter are for use on newborn records only, never on maternal records

Not coded here — never report together with this code.

congenital stenosis and stricture of bile ducts (Q44.3) (from P55)
Crigler-Najjar syndrome (E80.5) (from P55)
Dubin-Johnson syndrome (E80.6) (from P55)
Gilbert syndrome (E80.4) (from P55)
hereditary hemolytic anemias (D55-D58) (from P55)

Not included here — may be reported together when both conditions exist.

congenital malformations, deformations and chromosomal abnormalities (Q00-Q99) (from P55)
endocrine, nutritional and metabolic diseases (E00-E88) (from P55)
injury, poisoning and certain other consequences of external causes (S00-T88) (from P55)
neoplasms (C00-D49) (from P55)
tetanus neonatorum (A33) (from P55)

Anemia, congenital, due to isoimmunization NOS
Anemia, erythroblastic, newborn
Disease, diseased, hemolytic
Erythroblastosis
Isoimmunization NEC, newborn
Jaundice, newborn, due to or associated with, hemolytic disease
Jaundice, newborn, due to or associated with, incompatibility, maternal/fetal NOS
Jaundice, newborn, due to or associated with, isoimmunization NOS