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

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ICD-9-CM Index to Diseases (FY11) lymphocytic depletion (M9653/3) 201.7 diffuse fibrosis (M9654/3) 201.7 reticular type (M9655/3) 201.7 predominance (M9651/3) 201.4 lymphocytic-histiocytic predominance (M9651/3) 201.4 mixed cellularity (M9652/3) 201.6 nodular sclerosis (M9656/3) 201.5 cellular phase (M9657/3) 201.5 Hodgson's 441.9 ruptured 441.5 Hoffa (-Kastert) (liposynovitis prepatellaris) 272.8 Holla (see also Spherocytosis) 282.0 homozygous-Hb-S 282.61 hoof and mouth 078.4 hookworm (see also Ancylostomiasis) 126.9 Horton's (temporal arteritis) 446.5 host-versus-graft (immune or nonimmune cause) 279.50 HPFH (hereditary persistence of fetal hemoglobin) ("Swiss variety") 282.7 Huchard's (continued arterial hypertension) 401.9 Huguier's (uterine fibroma) 218.9 human immunodeficiency (virus) 042 hunger 251.1 Hunt's dyssynergia cerebellaris myoclonica 334.2 herpetic geniculate ganglionitis 053.11 Huntington's 333.4 Huppert's (multiple myeloma) (M9730/3) 203.0 Hurler's (mucopolysaccharidosis I) 277.5 Hutchinson's, meaning angioma serpiginosum 709.1 cheiropompholyx 705.81 prurigo estivalis 692.72 Hutchinson-Boeck (sarcoidosis) 135 Hutchinson-Gilford (progeria) 259.8 hyaline (diffuse) (generalized) 728.9 membrane (lung) (newborn) 769 hydatid (see also Echinococcus) 122.9 Hyde's (prurigo nodularis) 698.3 hyperkinetic (see also Hyperkinesia) 314.9 heart 429.82 hypertensive (see also Hypertension) 401.9 hypophysis 253.9 hyperfunction 253.1 hypofunction 253.2 iceland (epidemic neuromyasthenia) 049.8 I cell 272.7 ill-defined 799.89 immunologic NEC 279.9 immunoproliferative 203.8 inclusion 078.5 salivary gland 078.5 infancy, early NEC 779.9 infective NEC 136.9 inguinal gland 289.9 internal semilunar cartilage, cystic 717.5 426
ICD-9-CM Index to Diseases (FY11) intervertebral disc 722.90 with myelopathy 722.70 cervical, cervicothoracic 722.91 with myelopathy 722.71 lumbar, lumbosacral 722.93 with myelopathy 722.73 thoracic, thoracolumbar 722.92 with myelopathy 722.72 intestine 569.9 functional 564.9 congenital 751.3 psychogenic 306.4 lardaceous 277.39 organic 569.9 protozoal NEC 007.9 iris 364.9 specified NEC 364.89 iron metabolism (see also Hemochromatosis) 275.03 storage (see also Hemochromatosis) 275.03 Isambert's (see also Tuberculosis, larynx) 012.3 Iselin's (osteochondrosis, fifth metatarsal) 732.5 island (scrub typhus) 081.2 itai-itai 985.5 Jadassohn's (maculopapular erythroderma) 696.2 Jadassohn-Pellizari's (anetoderma) 701.3 Jakob-Creutzfeldt (CJD) 046.19 with dementia with behavioral disturbance 046.19 [294.11] without behavioral disturbance 046.19 [294.10] familial 046.19 iatrogenic 046.19 specified NEC 046.19 sporadic 046.19 variant (vCJD) 046.11 with dementia with behavioral disturbance 046.11 [294.11] without behavioral disturbance 046.11 [294.10] Jaksch (-Luzet) (pseudoleukemia infantum) 285.8 Janet's 300.89 Jansky-Bielschowsky 330.1 jaw NEC 526.9 fibrocystic 526.2 Jensen's 363.05 Jeune's (asphyxiating thoracic dystrophy) 756.4 Jigger 134.1 Johnson-Stevens (erythema multiforme exudativum) 695.13 joint NEC 719.9 ankle 719.97 Charcôt 094.0 [713.5] degenerative (see also Osteoarthrosis) 715.9 multiple 715.09 spine (see also Spondylosis) 721.90 elbow 719.92 foot 719.97 hand 719.94 427
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