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

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ICD-9-CM Index to Diseases (FY11) osseous, major 731.3 osteochondral NEC 738.8 ostium primum 745.61 secundum 745.5 pericardium 746.89 peroxidase-binding 246.1 placental blood supply - see Placenta, insufficiency platelet (qualitative) 287.1 constitutional 286.4 postural, spine 737.9 protan 368.51 pulmonic cusps, congenital 746.00 renal pelvis 753.9 obstructive 753.29 specified type NEC 753.3 respiratory system, congenital 748.9 specified type NEC 748.8 retina, retinal 361.30 with detachment (see also Detachment, retina, with retinal defect) 361.00 multiple 361.33 with detachment 361.02 nerve fiber bundle 362.85 single 361.30 with detachment 361.01 septal (closure) (heart) NEC 745.9 acquired 429.71 atrial 745.5 specified type NEC 745.8 speech NEC 784.59 developmental 315.39 late effect of cerebrovascular disease - see Late effect(s) (of) cerebrovascular disease, speech and language deficit secondary to organic lesion 784.59 Taussig-Bing (transposition, aorta and overriding pulmonary artery) 745.11 teeth, wedge 521.20 thyroid hormone synthesis 246.1 tritan 368.53 ureter 753.9 obstructive 753.29 vascular (acquired) (local) 459.9 congenital (peripheral) NEC 747.60 gastrointestinal 747.61 lower limb 747.64 renal 747.62 specified NEC 747.69 spinal 747.82 upper limb 747.63 ventricular septal 745.4 with pulmonary stenosis or atresia, dextraposition of aorta, and hypertrophy of right ventricle 745.2 acquired 429.71 atrioventricular canal type 745.69 between infundibulum and anterior portion 745.4 in tetralogy of Fallot 745.2 isolated anterior 745.4 324
ICD-9-CM Index to Diseases (FY11) vision NEC 369.9 visual field 368.40 arcuate 368.43 heteronymous, bilateral 368.47 homonymous, bilateral 368.46 localized NEC 368.44 nasal step 368.44 peripheral 368.44 sector 368.43 voice and resonance 784.40 wedge, teeth (abrasion) 521.20 Defeminization syndrome 255.2 Deferentitis 608.4 gonorrheal (acute) 098.14 chronic or duration of 2 months or over 098.34 Defibrination syndrome (see also Fibrinolysis) 286.6 Deficiency, deficient 3-beta-hydroxysteroid dehydrogenase 255.2 6-phosphogluconic dehydrogenase (anemia) 282.2 11-beta-hydroxylase 255.2 17-alpha-hydroxylase 255.2 18-hydroxysteroid dehydrogenase 255.2 20-alpha-hydroxylase 255.2 21-hydroxylase 255.2 AAT (alpha-1 antitrypsin) 273.4 abdominal muscle syndrome 756.79 accelerator globulin (Ac G) (blood) (see also Defect, coagulation) 286.3 AC globulin (congenital) (see also Defect, coagulation) 286.3 acquired 286.7 activating factor (blood) (see also Defect, coagulation) 286.3 adenohypophyseal 253.2 adenosine deaminase 277.2 aldolase (hereditary) 271.2 alpha-1-antitrypsin 273.4 alpha-1-trypsin inhibitor 273.4 alpha-fucosidase 271.8 alpha-lipoprotein 272.5 alpha-mannosidase 271.8 amino acid 270.9 anemia - see Anemia, deficiency aneurin 265.1 with beriberi 265.0 antibody NEC 279.00 antidiuretic hormone 253.5 antihemophilic factor (A) 286.0 B 286.1 C 286.2 globulin (AHG) NEC 286.0 antithrombin III 289.81 antitrypsin 273.4 argininosuccinate synthetase or lyase 270.6 ascorbic acid (with scurvy) 267 autoprothrombin I (see also Defect, coagulation) 286.3 II 286.1 325
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2011 ICD-9-CM Diagnosis Disease Index - SCAN Health Plan

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