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

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ICD-9-CM Index to Diseases (FY11) luteinizing hormone (LH) 253.4 lysosomal alpha-1, 4 glucosidase 271.0 magnesium 275.2 mannosidase 271.8 medium chain acyl CoA dehydrogenase (MCAD) 277.85 melanocyte-stimulating hormone (MSH) 253.4 menadione (vitamin K) 269.0 newborn 776.0 mental (familial) (hereditary) (see also Retardation, mental) 319 methylenetetrahydrofolate reductase (MTHFR) 270.4 mineral NEC 269.3 mineralocorticoid 255.42 molybdenum 269.3 moral 301.7 multiple, syndrome 260 myocardial (see also Insufficiency, myocardial) 428.0 myophosphorylase 271.0 NADH (DPNH) -methemoglobin-reductase (congenital) 289.7 NADH diaphorase or reductase (congenital) 289.7 neck V48.1 niacin (amide) (-tryptophan) 265.2 nicotinamide 265.2 nicotinic acid (amide) 265.2 nose V48.8 number of teeth (see also Anodontia) 520.0 nutrition, nutritional 269.9 specified NEC 269.8 ornithine transcarbamylase 270.6 ovarian 256.39 oxygen (see also Anoxia) 799.02 pantothenic acid 266.2 parathyroid (gland) 252.1 phenylalanine hydroxylase 270.1 phosphoenolpyruvate carboxykinase 271.8 phosphofructokinase 271.2 phosphoglucomutase 271.0 phosphohexosisomerase 271.0 phosphomannomutase 271.8 phosphomannose isomerase 271.8 phosphomannosyl mutase 271.8 phosphorylase kinase, liver 271.0 pituitary (anterior) 253.2 posterior 253.5 placenta - see Placenta, insufficiency plasma cell 279.00 protein (paraproteinemia) (pyroglobulinemia) 273.8 gamma globulin 279.00 thromboplastin antecedent (PTA) 286.2 component (PTC) 286.1 platelet NEC 287.1 constitutional 286.4 polyglandular 258.9 potassium (K) 276.8 proaccelerin (congenital) (see also Defect, congenital) 286.3 330
ICD-9-CM Index to Diseases (FY11) acquired 286.7 proconvertin factor (congenital) (see also Defect, coagulation) 286.3 acquired 286.7 prolactin 253.4 protein 260 anemia 281.4 C 289.81 plasma - see Deficiency, plasma, protein S 289.81 prothrombin (congenital) (see also Defect, coagulation) 286.3 acquired 286.7 Prower factor (see also Defect, coagulation) 286.3 PRT 277.2 pseudocholinesterase 289.89 psychobiological 301.6 PTA 286.2 PTC 286.1 purine nucleoside phosphorylase 277.2 pyracin (alpha) (beta) 266.1 pyridoxal 266.1 pyridoxamine 266.1 pyridoxine (derivatives) 266.1 pyruvate carboxylase 271.8 pyruvate dehydrogenase 271.8 pyruvate kinase (PK) 282.3 riboflavin (vitamin B 2) 266.0 saccadic eye movements 379.57 salivation 527.7 salt 276.1 secretion ovary 256.39 salivary gland (any) 527.7 urine 788.5 selenium 269.3 serum antitrypsin, familial 273.4 protein (congenital) 273.8 short chain acyl CoA dehydrogenase (SCAD) 277.85 short stature homeobox gene (SHOX) with dyschondrosteosis 756.89 short stature (idiopathic) 783.43 Turner's syndrome 758.6 smooth pursuit movements (eye) 379.58 sodium (Na) 276.1 SPCA (see also Defect, coagulation) 286.3 specified NEC 269.8 stable factor (congenital) (see also Defect, coagulation) 286.3 acquired 286.7 Stuart (-Prower) factor (see also Defect, coagulation) 286.3 sucrase 271.3 sucrase-isomaltase 271.3 sulfite oxidase 270.0 syndrome, multiple 260 thiamine, thiaminic (chloride) 265.1 331
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