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-
2012 ICD-9-CM Diagnosis Code 773.1
Hemolytic disease of fetus or newborn due to ABO isoimmunization
- Short description: NB hemolyt dis-abo isoim.
- ICD-9-CM 773.1 is a billable medical code that can be used to specify a diagnosis on a reimbursement claim.
- You are viewing the 2012 version of ICD-9-CM 773.1.
- More recent version(s) of ICD-9-CM 773.1: 2013.
Applies To
- ABO hemolytic disease
- ABO isoimmunization
- Anemia due to ABO:
- antibodies
- isoimmunization
- maternal/fetal incompatibility
- Erythroblastosis (fetalis) due to ABO:
- antibodies
- isoimmunization
- maternal/fetal incompatibility
- Hemolytic disease (fetus) (newborn) due to ABO:
- antibodies
- isoimmunization
- maternal/fetal incompatibility
- Jaundice due to ABO:
- antibodies
- isoimmunization
- maternal/fetal incompatibility
Convert 773.1 to ICD-10-CM 
ICD-9-CM 773.1 converts approximately to:
- 2013 ICD-10-CM P55.1 ABO isoimmunization of newborn
ICD-9-CM Volume 2 Index entries containing back-references to 773.1:
- ABO
hemolytic disease 773.1
- Anemia 285.9
- Disease, diseased - see also Syndrome
- Erythroblastosis (fetalis) (newborn) 773.2
- Immunization
- ABO
affecting management of pregnancy 656.2- fetus or newborn 773.1
- Incompatibility
- Isoimmunization NEC (see also Incompatibility) 656.2
- Jaundice (yellow) 782.4
- fetus or newborn 774.6
due to or associated with
ABO- antibodies 773.1
- incompatibility, maternal/fetal 773.1
- isoimmunization 773.1
- 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
- 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
ICD-9-CM codes are used in medical billing and coding to describe diseases, injuries, symptoms and conditions. ICD-9-CM 773.1 is one of thousands of ICD-9-CM codes used in healthcare. Although ICD-9-CM and CPT codes are largely numeric, they differ in that CPT codes describe medical procedures and services. Can't find a code? Start at the root of ICD-9-CM, check the 2012 ICD-9-CM Index or use the search engine at the top of this page to lookup any code.
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