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2009 ICD-9-CM
Diseases and Injuries
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Deficiency, deficient | |
ICSH (interstitial cell-stimulating hormone) 253.4 | |
immunity NEC 279.3 | |
cell-mediated 279.10 | |
with | |
hyperimmunoglobulinemia 279.2 | |
thrombocytopenia and eczema 279.12 | |
specified NEC 279.19 | |
combined (severe) 279.2 | |
syndrome 279.2 | |
common variable 279.06 | |
humoral NEC 279.00 | |
IgA (secretory) 279.01 | |
IgG 279.03 | |
IgM 279.02 | |
immunoglobulin, selective NEC 279.03 | |
IgA 279.01 | |
IgG 279.03 | |
IgM 279.02 | |
inositol (B complex) 266.2 | |
interferon 279.4 | |
internal organ V47.0 | |
interstitial cell-stimulating hormone (ICSH) 253.4 | |
intrinsic factor (Castle's) (congenital) 281.0 | |
intrinsic (urethral) sphincter (ISD) 599.82 | |
invertase 271.3 | |
iodine 269.3 | |
iron, anemia 280.9 | |
labile factor (congenital) (see also Defect, coagulation) 286.3 | |
acquired 286.7 | |
lacrimal fluid (acquired) 375.15 | |
congenital 743.64 | |
lactase 271.3 | |
laki-Lorand factor (see also Defect, coagulation) 286.3 | |
lecithin-cholesterol acyltranferase 272.5 | |
LH (luteinizing hormone) 253.4 | |
limb V49.0 | |
lower V49.0 | |
congenital (see also Deficiency, lower limb, congenital) 755.30 | |
upper V49.0 | |
congenital (see also Deficiency, upper limb, congenital) 755.20 | |
lipocaic 577.8 | |
lipoid (high-density) 272.5 | |
lipoprotein (familial) (high-density) 272.5 | |
liver phosphorylase 271.0 | |
long chain 3-hydroxyacyl CoA dehydrogenase (LCHAD) 277.85 | |
long chain/very long chain acyl CoA dehydrogenase (LCAD, VLCAD) 277.85 | |
lower limb V49.0 | |
congenital 755.30 | |
with complete absence of distal elements 755.31 | |
longitudinal (complete) (partial) (with distal deficiencies, incomplete) 755.32 | |