2006 ICD-9-CM Volume 1 Diagnosis Codes Home > Diseases Of Blood And Blood-Forming Organs 280-289 > Acquired Hemolytic Anemias 283.* > 2006 ICD-9-CM Diagnosis 283.9 Acquired hemolytic anemia unspecified View the most recent version of ICD-9-CM 283.9 283.9 is a specific code that can be used to specify a diagnosis 283.9 contains 24 index entries View the ICD-9-CM Volume 1 283.* hierarchy Alternate Terminology Acquired hemolytic anemia NOS Chronic idiopathic hemolytic anemia  Index entries containing 283.9: Abrami's disease (acquired hemolytic jaundice) 283.9 Acholuric jaundice (familial) (splenomegalic) (see also Spherocytosis) 282.0 acquired 283.9 Anemia 285.9 Dyke-Young type (secondary) (symptomatic) 283.9 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 autoimmune 283.0 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 late 773.5 Lederer's (acquired infectious hemolytic anemia) 283.19 autoimmune (acquired) 283.0 chronic 282.9 idiopathic 283.9 cold type (secondary) (symptomatic) 283.0 congenital (spherocytic) (see also Spherocytosis) 282.0 nonspherocytic - see Anemia, hemolytic, nonspherocytic, congenital drug-induced 283.0 enzyme deficiency 282.2 due to cardiac conditions 283.19 drugs 283.0 enzyme deficiency NEC 282.3 drug-induced 282.2 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 congenital or hereditary NEC 282.3 glucose-6-phosphate dehydrogenase deficiency 282.2 pyruvate kinase (PK) deficiency 282.3 type I 282.2 type II 282.3 type I 282.2 type II 282.3 of or complicating pregnancy 648.2 resulting from presence of shunt or other internal prosthetic device 283.19 secondary 283.19 autoimmune 283.0 sickle-cell - see Disease, sickle-cell Stransky-Regala type (Hb-E) (see also Disease, hemoglobin) 282.7 symptomatic 283.19 autoimmune 283.0 acute 285.1 toxic (acquired) 283.19 uremic (adult) (child) 283.11 warm type (secondary) (symptomatic) 283.0 idiopathic 285.9 hemolytic, chronic 283.9 Disease, diseased - see also Syndrome Abrami's (acquired hemolytic jaundice) 283.9 Widal-Abrami (acquired hemolytic jaundice) 283.9 Dyke-Young anemia or syndrome (acquired macrocytic hemolytic anemia) (secondary) (symptomatic) 283.9 Hayem-Widal syndrome (acquired hemolytic jaundice) 283.9 Icteroanemia, hemolytic (acquired) 283.9 congenital (see also Spherocytosis) 282.0 Icterus (see also Jaundice) 782.4 hematogenous (acquired) 283.9 hemolytic (acquired) 283.9 congenital (see also Spherocytosis) 282.0 Jaundice (yellow) 782.4 acholuric (familial) (splenomegalic) (see also Spherocytosis) 282.0 acquired 283.9 hematogenous 283.9 hemolytic (acquired) 283.9 congenital (see also Spherocytosis) 282.0 Syndrome - see also Disease Dyke-Young (acquired macrocytic hemolytic anemia) 283.9 Hayem-Widal (acquired hemolytic jaundice) 283.9 Widal (-Abrami) (acquired hemolytic jaundice) 283.9 Widal (-Abrami) syndrome (acquired hemolytic jaundice) 283.9