2011 ICD-9-CM Diagnosis Disease Index - SCAN Health Plan

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ICD-9-CM Index to Diseases (FY11) fetal 678.0 following blood loss, affecting newborn 776.5 fetus or newborn due to ABO antibodies 773.1 incompatibility, maternal/fetal 773.1 isoimmunization 773.1 Rh antibodies 773.0 incompatibility, maternal/fetal 773.0 isoimmunization 773.0 following fetal blood loss 776.5 fish tapeworm (D. latum) infestation 123.4 folate (folic acid) deficiency 281.2 dietary 281.2 drug-induced 281.2 folate malabsorption, congenital 281.2 folic acid deficiency 281.2 dietary 281.2 drug-induced 281.2 G-6-PD 282.2 general 285.9 glucose-6-phosphate dehydrogenase deficiency 282.2 glutathione-reductase deficiency 282.2 goat's milk 281.2 granulocytic 288.09 Heinz-body, congenital 282.7 hemoglobin deficiency 285.9 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 92
ICD-9-CM Index to Diseases (FY11) 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 toxic (acquired) 283.19 uremic (adult) (child) 283.11 warm type (secondary) (symptomatic) 283.0 hemorrhagic (chronic) 280.0 acute 285.1 HEMPAS 285.8 hereditary erythroblast multinuclearity-positive acidified serum test 285.8 Herrick's (hemoglobin S disease) 282.61 hexokinase deficiency 282.3 high A 2 282.49 hookworm (see also Ancylostomiasis) 126.9 hypochromic (idiopathic) (microcytic) (normoblastic) 280.9 with iron loading 285.0 due to blood loss (chronic) 280.0 acute 285.1 familial sex linked 285.0 pyridoxine-responsive 285.0 hypoplasia, red blood cells 284.81 congenital or familial 284.01 hypoplastic (idiopathic) 284.9 congenital 284.01 93
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