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2009 ICD-9-CM

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Polycytosis cryptogenica 289.0
Polydactylism, polydactyly 755.00
Polydipsia 783.5
Polydystrophic oligophrenia 277.5
Polyembryoma (M9072/3) - see Neoplasm, by site, malignant
Polygalactia 676.6
Polyglandular
Polyhydramnios (see also Hydramnios) 657
Polymastia 757.6
Polymenorrhea 626.2
Polymicrogyria 742.2
Polymyalgia 725
Polymyositis (acute) (chronic) (hemorrhagic) 710.4
Polyneuritis, polyneuritic (see also Polyneuropathy) 356.9
Polyneuropathy (peripheral) 356.9
Polyonychia 757.5
Polyopia 368.2
Polyorchism, polyorchidism (three testes) 752.89
Polyorrhymenitis (peritoneal) (see also Polyserositis) 568.82
Polyostotic fibrous dysplasia 756.54
Polyotia 744.1
Polyp, polypus
Polyphagia 783.6
Polypoid - see condition
Polyposis - see also Polyp
Polyradiculitis (acute) 357.0
Polyradiculoneuropathy (acute) (segmentally demyelinating) 357.0
Polysarcia 278.00
Polyserositis (peritoneal) 568.82
Polysialia 527.7
Polysplenia syndrome 759.0
Polythelia 757.6
Polytrichia (see also Hypertrichosis) 704.1
Polyunguia (congenital) 757.5
Polyuria 788.42
Pompe's disease (glycogenosis II) 271.0
Pompholyx 705.81
Poncet's disease (tuberculous rheumatism) (see also Tuberculosis) 015.9
Pond fracture - see Fracture, skull, vault
Ponos 085.0
Pons, pontine - see condition
Poor
Poradenitis, nostras 099.1
Porencephaly (congenital) (developmental) (true) 742.4
Porocephaliasis 134.1
Porokeratosis 757.39
Poroma, eccrine (M8402/0) - see Neoplasm, skin, benign
Porphyria (acute) (congenital) (constitutional) (erythropoietic) (familial) (hepatica) (idiopathic) (idiosyncratic) (intermittent) (latent) (mixed hepatic) (photosensitive) (South African genetic) (Swedish) 277.1
Porphyrinuria (acquired) (congenital) (secondary) 277.1
Porphyruria (acquired) (congenital) 277.1
 
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