Hemolytic disease of fetus or newborn due to other and unspecified isoimmunization
Convert to ICD-10-CM:
773.2 converts approximately to:
- 2015/16 ICD-10-CM P55.8 Other hemolytic diseases of newborn
Or:
- 2015/16 ICD-10-CM P55.9 Hemolytic disease of newborn, unspecified
ICD-9-CM Volume 2 Index entries containing back-references to
773.2:
- Anemia 285.9
- congenital (following fetal blood loss) 776.5
- aplastic 284.01
- due to isoimmunization NEC 773.2
- Heinz-body 282.7
- hereditary hemolytic NEC 282.9
- nonspherocytic
- pernicious 281.0
- spherocytic (see also Spherocytosis) 282.0
- erythroblastic
- familial 282.44
- fetus or newborn (see also Disease, hemolytic) 773.2
- hemolytic 283.9
- acquired 283.9
- with hemoglobinuria NEC 283.2
- autoimmune (cold type) (idiopathic) (primary) (secondary) (symptomatic) (warm type) 283.0
- due to
- cold reactive antibodies 283.0
- drug exposure 283.0
- warm reactive antibodies 283.0
- fragmentation 283.19
- idiopathic (chronic) 283.9
- infectious 283.19
- non-autoimmune 283.10
- toxic 283.19
- traumatic cardiac 283.19
- acute 283.9
- due to enzyme deficiency NEC 282.3
- fetus or newborn (see also Disease, hemolytic) 773.2
- Lederer's (acquired infectious hemolytic anemia) 283.19
- autoimmune (acquired) 283.0
- chronic 282.9
- cold type (secondary) (symptomatic) 283.0
- congenital (spherocytic) (see also Spherocytosis) 282.0
- nonspherocytic - see Anemia, hemolytic, nonspherocytic, congenital
- drug-induced 283.0
- due to
- cardiac conditions 283.19
- drugs 283.0
- enzyme deficiency NEC 282.3
- presence of shunt or other internal prosthetic device 283.19
- thrombotic thrombocytopenic purpura 446.6
- elliptocytotic (see also Elliptocytosis) 282.1
- familial 282.9
- hereditary 282.9
- due to enzyme deficiency NEC 282.3
- specified NEC 282.8
- idiopathic (chronic) 283.9
- infectious (acquired) 283.19
- mechanical 283.19
- microangiopathic 283.19
- nonautoimmune 283.10
- nonspherocytic
- of or complicating pregnancy 648.2
- resulting from presence of shunt or other internal prosthetic device 283.19
- secondary 283.19
- sickle-cell - see Disease, sickle-cell
- Stransky-Regala type (Hb-E) (see also Disease, hemoglobin) 282.7
- symptomatic 283.19
- toxic (acquired) 283.19
- uremic (adult) (child) 283.11
- warm type (secondary) (symptomatic) 283.0
- newborn (see also Disease, hemolytic) 773.2
- due to isoimmunization (see also Disease, hemolytic) 773.2
- late, due to isoimmunization 773.5
- posthemorrhagic 776.5
- 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
- Incompatibility
- blood (group) (Duffy) (E) (K(ell)) (Kidd) (Lewis) (M) (N) (P) (S) NEC
- affecting management of pregnancy 656.2
- fetus or newborn 773.2
- infusion or transfusion reaction (see also Complications, transfusion) 999.75
- Isoimmunization NEC (see also Incompatibility) 656.2
- fetus or newborn 773.2
- 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