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2009 ICD-9-CM

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Deficiency, deficient
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
thrombokinase (see also Defect, coagulation) 286.3
newborn 776.0
thrombopoieten 287.39
thymolymphatic 279.2
thyroid (gland) 244.9
tocopherol 269.1
toe - see Absence, toe
tooth bud (see also Anodontia) 520.0
trunk V48.1
UDPG-glycogen transferase 271.0
upper limb V49.0
congenital 755.20
with complete absence of distal elements 755.21
longitudinal (complete) (partial) (with distal deficiencies, incomplete) 755.22
carpal(s) 755.28
combined humeral, radial, ulnar (incomplete) 755.23
humeral 755.24
metacarpal(s) 755.28
phalange(s) 755.29
meaning all digits 755.21
radial 755.26
radioulnar 755.25
ulnar 755.27
transverse (complete) (partial) 755.21
vascular 459.9
vasopressin 253.5
viosterol (see also Deficiency, calciferol) 268.9
vitamin (multiple) NEC 269.2
 
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