Home > 2006 ICD-9-CM Diagnosis Codes > Certain Conditions Originating In The Perinatal Period 760-779 > Other Conditions Originating In The Perinatal Period 764-779 > Other perinatal jaundice 774-
Specific code 2006 ICD-9-CM Diagnosis Code 774.31
nEonatal jaundice due to delayed conjugation in diseases classified elsewhere
  • Short description: NEONAT JAUND IN OTH DIS.
  • ICD-9-CM 774.31 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 774.31 should only be used for claims with a date of service on or before September 30, 2015. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes).
  • You are viewing the 2006 version of ICD-9-CM 774.31.
  • More recent version(s) of ICD-9-CM 774.31: 2007 2008 2009 2010 2011 2012 2013 2014 2015.
Convert to ICD-10-CM: 774.31 converts approximately to:
  • 2015/16 ICD-10-CM P59.8 Neonatal jaundice from other specified causes
Code First
  • Code first underlying diseases, as:
    • congenital hypothyroidism (243)
    • Crigler-Najjar syndrome (277.4)
    • Gilbert's syndrome (277.4)
ICD-9-CM Volume 2 Index entries containing back-references to 774.31:
  • Jaundice (yellow) 782.4
    • fetus or newborn 774.6
      • due to or associated with
        • ABO
        • absence or deficiency of enzyme system for bilirubin conjugation (congenital) 774.39
        • blood group incompatibility NEC 773.2
        • breast milk inhibitors to conjugation 774.39
          • associated with preterm delivery 774.2
        • bruising 774.1
        • Crigler-Najjar syndrome 277.4 [774.31]
        • delayed conjugation 774.30
          • associated with preterm delivery 774.2
          • development 774.39
        • drugs or toxins transmitted from mother 774.1
        • G-6-PD deficiency 282.2 [774.0]
        • galactosemia 271.1 [774.5]
        • Gilbert's syndrome 277.4 [774.31]
        • hepatocellular damage 774.4
        • hereditary hemolytic anemia (see also Anemia, hemolytic) 282.9 [774.0]
        • hypothyroidism, congenital 243 [774.31]
        • incompatibility, maternal/fetal NEC 773.2
        • infection 774.1
        • inspissated bile syndrome 774.4
        • isoimmunization NEC 773.2
        • mucoviscidosis 277.01 [774.5]
        • obliteration of bile duct, congenital 751.61 [774.5]
        • polycythemia 774.1
        • preterm delivery 774.2
        • red cell defect 282.9 [774.0]
        • Rh
        • spherocytosis (congenital) 282.0 [774.0]
        • swallowed maternal blood 774.1
      • physiological NEC 774.6
 774.30 ICD9Data.com 774.39 
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