Home > 2012 ICD-9-CM Diagnosis Codes > Certain Conditions Originating In The Perinatal Period 760-779 > Other Conditions Originating In The Perinatal Period 764-779 > Hemolytic disease of fetus or newborn due to isoimmunization 773-
Specific code 2012 ICD-9-CM Diagnosis Code 773.0
Hemolytic disease of fetus or newborn due to Rh isoimmunization
  • Short description: NB hemolyt dis:rh isoimm.
  • ICD-9-CM 773.0 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 773.0 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 2012 version of ICD-9-CM 773.0.
  • More recent version(s) of ICD-9-CM 773.0: 2013 2014 2015.
Convert to ICD-10-CM: 773.0 converts directly to:
  • 2015/16 ICD-10-CM P55.0 Rh isoimmunization of newborn
Approximate Synonyms
  • Hemolytic disease of fetus OR newborn due to RhD isoimmunization
  • Rh hemolytic disease, fetus or newborn
Applies To
  • Anemia due to RH:
    • antibodies
    • isoimmunization
    • maternal/fetal incompatibility
  • Erythroblastosis (fetalis) due to RH:
    • antibodies
    • isoimmunization
    • maternal/fetal incompatibility
  • Hemolytic disease (fetus) (newborn) due to RH:
    • antibodies
    • isoimmunization
    • maternal/fetal incompatibility
  • Jaundice due to RH:
    • antibodies
    • isoimmunization
    • maternal/fetal incompatibility
  • Rh hemolytic disease
  • Rh isoimmunization
ICD-9-CM Volume 2 Index entries containing back-references to 773.0:
  • Anemia 285.9
    • fetus or newborn
      • due to
        • ABO
        • Rh
          • antibodies 773.0
          • incompatibility, maternal/fetal 773.0
          • isoimmunization 773.0
      • following fetal blood loss 776.5
  • Antibodies
    • maternal (blood group) (see also Incompatibility) 656.2
      • anti-D, cord blood 656.1
        • fetus or newborn 773.0
  • Disease, diseased - see also Syndrome
    • hemolytic (fetus) (newborn) 773.2
      • autoimmune (cold type) (warm type) 283.0
      • due to or with
        • incompatibility
          • ABO (blood group) 773.1
          • blood (group) (Duffy) (Kell) (Kidd) (Lewis) (M) (S) NEC 773.2
          • Rh (blood group) (factor) 773.0
        • Rh negative mother 773.0
      • unstable hemoglobin 282.7
  • Erythroblastosis (fetalis) (newborn) 773.2
    • due to
      • ABO
      • Rh
        • antibodies 773.0
        • incompatibility, maternal/fetal 773.0
        • isoimmunization 773.0
  • Icterus (see also Jaundice) 782.4
    • gravis (see also Necrosis, liver) 570
      • complicating pregnancy 646.7
        • affecting fetus or newborn 760.8
      • fetus or newborn NEC 773.0
      • obstetrical 646.7
        • affecting fetus or newborn 760.8
  • Immunization
    • Rh factor
      • affecting management of pregnancy 656.1
        • fetus or newborn 773.0
      • from transfusion (see also Complications, transfusion) 999.70
  • Immunodeficiency 279.3
    • to Rh factor
      • affecting management of pregnancy 656.1
        • fetus or newborn 773.0
  • Incompatibility
    • Rh (antigen) (C) (c) (D) (E) (e) (blood group) (factor)
      • affecting management of pregnancy 656.1
      • fetus or newborn 773.0
      • infusion or transfusion reaction (see also Complications, transfusion) 999.70
  • Isoimmunization NEC (see also Incompatibility) 656.2
    • fetus or newborn 773.2
      • ABO blood groups 773.1
      • Rhesus (Rh) factor 773.0
  • 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
          • antibodies 773.0
          • incompatibility, maternal/fetal 773.0
          • isoimmunization 773.0
        • spherocytosis (congenital) 282.0 [774.0]
        • swallowed maternal blood 774.1
      • physiological NEC 774.6
  • Rh antigen (C) (c) (D) (E) (e) (factor)
    • hemolytic disease 773.0
    • incompatibility, immunization, or sensitization
      • affecting management of pregnancy 656.1
      • fetus or newborn 773.0
      • transfusion reaction (see also Complications, transfusion) 999.70
    • negative mother, affecting fetus or newborn 773.0
 773 ICD9Data.com 773.1 
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