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

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ICD-9-CM Index to Diseases (FY11) 21-hydroxylase 255.2 abdominal wall, congenital 756.70 aorticopulmonary septum 745.0 aortic septal 745.0 atrial septal (ostium secundum type) 745.5 acquired 429.71 ostium primum type 745.61 sinus venosus 745.8 atrioventricular canal 745.69 septum 745.4 acquired 429.71 atrium secundum 745.5 acquired 429.71 auricular septal 745.5 acquired 429.71 bilirubin excretion 277.4 biosynthesis, testicular androgen 257.2 bridge 525.60 bulbar septum 745.0 butanol-insoluble iodide 246.1 chromosome - see Anomaly, chromosome circulation (acquired) 459.9 congenital 747.9 newborn 747.9 clotting NEC (see also Defect, coagulation) 286.9 coagulation (factor) (see also Deficiency, coagulation factor) 286.9 with abortion - see Abortion, by type, with hemorrhage ectopic pregnancy (see also categories 634-638) 639.1 molar pregnancy (see also categories 630-632) 639.1 acquired (any) 286.7 antepartum or intrapartum 641.3 affecting fetus or newborn 762.1 causing hemorrhage of pregnancy or delivery 641.3 complicating pregnancy, childbirth, or puerperium 649.3 due to liver disease 286.7 vitamin K deficiency 286.7 newborn, transient 776.3 postpartum 666.3 specified type NEC 286.9 conduction (heart) 426.9 bone (see also Deafness, conductive) 389.00 congenital, organ or site NEC - see also Anomaly circulation 747.9 Descemet's membrane 743.9 specified type NEC 743.49 diaphragm 756.6 ectodermal 757.9 esophagus 750.9 pulmonic cusps - see Anomaly, heart valve respiratory system 748.9 specified type NEC 748.8 crown 525.60 cushion endocardial 745.60 322
ICD-9-CM Index to Diseases (FY11) dental restoration 525.60 dentin (hereditary) 520.5 Descemet's membrane (congenital) 743.9 acquired 371.30 specific type NEC 743.49 deutan 368.52 developmental - see also Anomaly, by site cauda equina 742.59 left ventricle 746.9 with atresia or hypoplasia of aortic orifice or valve, with hypoplasia of ascending aorta 746.7 in hypoplastic left heart syndrome 746.7 testis 752.9 vessel 747.9 diaphragm with elevation, eventration, or hernia - see Hernia, diaphragm congenital 756.6 with elevation, eventration, or hernia 756.6 gross (with elevation, eventration, or hernia) 756.6 ectodermal, congenital 757.9 Eisenmenger's (ventricular septal defect) 745.4 endocardial cushion 745.60 specified type NEC 745.69 esophagus, congenital 750.9 extensor retinaculum 728.9 fibrin polymerization (see also Defect, coagulation) 286.3 filling biliary tract 793.3 bladder 793.5 dental 525.60 gallbladder 793.3 kidney 793.5 stomach 793.4 ureter 793.5 fossa ovalis 745.5 gene, carrier (suspected) of V83.89 Gerbode 745.4 glaucomatous, without elevated tension 365.89 Hageman (factor) (see also Defect, coagulation) 286.3 hearing (see also Deafness) 389.9 high grade 317 homogentisic acid 270.2 interatrial septal 745.5 acquired 429.71 interauricular septal 745.5 acquired 429.71 interventricular septal 745.4 with pulmonary stenosis or atresia, dextraposition of aorta, and hypertrophy of right ventricle 745.2 acquired 429.71 in tetralogy of Fallot 745.2 iodide trapping 246.1 iodotyrosine dehalogenase 246.1 kynureninase 270.2 learning, specific 315.2 major osseous 731.3 mental (see also Retardation, mental) 319 323
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