P61.9

Perinatal hematological disorder, unspecified

Billable / specific

P61.9 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 P61)
Crigler-Najjar syndrome (E80.5) (from P61)
Dubin-Johnson syndrome (E80.6) (from P61)
Gilbert syndrome (E80.4) (from P61)
hereditary hemolytic anemias (D55-D58) (from P61)
transient hypogammaglobulinemia of infancy (D80.7) (from P61)

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

congenital malformations, deformations and chromosomal abnormalities (Q00-Q99) (from P61)
endocrine, nutritional and metabolic diseases (E00-E88) (from P61)
injury, poisoning and certain other consequences of external causes (S00-T88) (from P61)
neoplasms (C00-D49) (from P61)
tetanus neonatorum (A33) (from P61)