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2009 ICD-9-CM

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Microphakia (congenital) 743.36
Microphthalmia (congenital) (see also Microphthalmos) 743.10
Microphthalmos (congenital) 743.10
Micropsia 368.14
Microsporidiosis 136.8
Microsporon furfur infestation 111.0
Microsporosis (see also Dermatophytosis) 110.9
Microstomia (congenital) 744.84
Microthelia 757.6
Microthromboembolism - see Embolism
Microtia (congenital) (external ear) 744.23
Microtropia 378.34
Micturition
Middle
Midplane - see condition
Miescher's disease 709.3
Miescher-Leder syndrome or granulomatosis 709.3
Mieten's syndrome 759.89
Migraine (idiopathic) 346.9
Migrant, social V60.0
Migratory, migrating - see also condition
Mikulicz's disease or syndrome (dryness of mouth, absent or decreased lacrimation) 527.1
Milian atrophia blanche 701.3
Miliaria (crystallina) (rubra) (tropicalis) 705.1
Miliary - see condition
Milium (see also Cyst, sebaceous) 706.2
Milk
Milkers' nodes 051.1
Milk-leg (deep vessels) 671.4
Milkman (-Looser) disease or syndrome (osteomalacia with pseudofractures) 268.2
Milky urine (see also Chyluria) 791.1
Millar's asthma (laryngismus stridulus) 478.75
Millard-Gubler paralysis or syndrome 344.89
Millard-Gubler-Foville paralysis 344.89
Miller-Dieker syndrome 758.33
Miller's disease (osteomalacia) 268.2
Miller Fisher's syndrome 357.0
Milles' syndrome (encephalocutaneous angiomatosis) 759.6
Mills' disease 335.29
Millstone makers' asthma or lung 502
Milroy's disease (chronic hereditary edema) 757.0
Miners' - see also condition
Minkowski-Chauffard syndrome (see also Spherocytosis) 282.0
Minor - see condition
Minor's disease 336.1
Minot's disease (hemorrhagic disease, newborn) 776.0
Minot-von Willebrand (-Jürgens) disease or syndrome (angiohemophilia) 286.4
Minus (and plus) hand (intrinsic) 736.09
Miosis (persistent) (pupil) 379.42
Mirizzi's syndrome (hepatic duct stenosis) (see also Obstruction, biliary) 576.2
 
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