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

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ICD-9-CM Index to Diseases (FY11) affecting fetus or newborn 763.1 shoulder (girdle) 660.4 affecting fetus or newborn 763.1 uterine NEC 661.4 affecting fetus or newborn 763.7 Dystonia acute due to drugs 333.72 neuroleptic-induced acute 333.72 deformans progressiva 333.6 lenticularis 333.6 musculorum deformans 333.6 torsion (idiopathic) 333.6 acquired 333.79 fragments (of) 333.89 genetic 333.6 symptomatic 333.79 Dystonic movements 781.0 Dystopia kidney 753.3 Dystrophy, dystrophia 783.9 adiposogenital 253.8 asphyxiating thoracic 756.4 Becker's type 359.22 brevicollis 756.16 Bruch's membrane 362.77 cervical (sympathetic) NEC 337.09 chondro-osseus with punctate epiphyseal dysplasia 756.59 choroid (hereditary) 363.50 central (areolar) (partial) 363.53 total (gyrate) 363.54 circinate 363.53 circumpapillary (partial) 363.51 total 363.52 diffuse partial 363.56 total 363.57 generalized partial 363.56 total 363.57 gyrate central 363.54 generalized 363.57 helicoid 363.52 peripapillary - see Dystrophy, choroid, circumpapillary serpiginous 363.54 cornea (hereditary) 371.50 anterior NEC 371.52 Cogan's 371.52 combined 371.57 crystalline 371.56 endothelial (Fuchs') 371.57 epithelial 371.50 juvenile 371.51 microscopic cystic 371.52 granular 371.53 506
ICD-9-CM Index to Diseases (FY11) lattice 371.54 macular 371.55 marginal (Terrien's) 371.48 meesman's 371.51 microscopic cystic (epithelial) 371.52 nodular, Salzmann's 371.46 polymorphous 371.58 posterior NEC 371.58 ring-like 371.52 Salzmann's nodular 371.46 stromal NEC 371.56 dermatochondrocorneal 371.50 Duchenne's 359.1 due to malnutrition 263.9 Erb's 359.1 familial hyperplastic periosteal 756.59 osseous 277.5 foveal 362.77 Fuchs', cornea 371.57 Gowers' muscular 359.1 hair 704.2 hereditary, progressive muscular 359.1 hypogenital, with diabetic tendency 759.81 Landouzy-Déjérine 359.1 Leyden-Möbius 359.1 mesodermalis congenita 759.82 muscular 359.1 congenital (hereditary) 359.0 myotonic 359.22 distal 359.1 Duchenne's 359.1 Erb's 359.1 fascioscapulohumeral 359.1 Gowers' 359.1 hereditary (progressive) 359.1 Landouzy-Déjérine 359.1 limb-girdle 359.1 myotonic 359.21 progressive (hereditary) 359.1 Charcôt-Marie-Tooth 356.1 pseudohypertrophic (infantile) 359.1 myocardium, myocardial (see also Degeneration, myocardial) 429.1 myotonic 359.21 myotonica 359.21 nail 703.8 congenital 757.5 neurovascular (traumatic) (see also Neuropathy, peripheral, autonomic) 337.9 nutritional 263.9 ocular 359.1 oculocerebrorenal 270.8 oculopharyngeal 359.1 ovarian 620.8 papillary (and pigmentary) 701.1 pelvicrural atrophic 359.1 pigmentary (see also Acanthosis) 701.2 507
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2011 ICD-9-CM Diagnosis Disease Index - SCAN Health Plan

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