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2008 ICD-9-CM Volume 1 Diagnosis Codes Home > Diseases Of The Blood And Blood-Forming Organs 280-289 > Purpura And Other Hemorrhagic Conditions 287.* > 2008 ICD-9-CM Diagnosis 287.1 Qualitative platelet defects A congenital bleeding disorder with prolonged bleeding time, absence of aggregation of platelets in response to most agents, especially ADP, and impaired or absent clot retraction. Platelet membranes are deficient in or have a defect in the glycoprotein IIb-IIIa complex (PLATELET GLYCOPROTEIN GPIIB-IIIA COMPLEX). A familial coagulation disorder characterized by a prolonged bleeding time, unusually large platelets, and impaired prothrombin consumption. Disorders caused by abnormalities in platelet count or function. 287.1 is a specific code that can be used to specify a diagnosis 287.1 contains 16 index entries View the ICD-9-CM Volume 1 287.* hierarchy 287.1 also known as: Thrombasthenia (hemorrhagic) (hereditary) Thrombocytasthenia Thrombocytopathy (dystrophic) Thrombopathy (Bernard-Soulier) 287.1 excludes: von Willebrand's disease (286.4) Index entries containing 287.1: Bernard-Soulier disease or thrombopathy 287.1 Defect, defective 759.9 platelet (qualitative) 287.1 constitutional 286.4 Deficiency, deficient platelet NEC 287.1 constitutional 286.4 Diacyclothrombopathia 287.1 Disease, diseased - see also Syndrome Bernard-Soulier (thrombopathy) 287.1 Glanzmann's (hereditary hemorrhagic thrombasthenia) 287.1 Naegeli's 287.1 Disorder - see also Disease platelets (blood) 287.1 Dysfunction platelets (blood) 287.1 Glanzmann (-Naegeli) disease or thrombasthenia 287.1 Naegeli's disease (hereditary hemorrhagic thrombasthenia 287.1 Thrombasthenia (Glanzmann's) (hemorrhagic) (hereditary) 287.1 Thromboasthenia (Glanzmann's) (hemorrhagic) (hereditary) 287.1 Thrombocytasthenia (Glanzmann's) 287.1 Thrombocytopathy (dystrophic) (granulopenic) 287.1 Thrombopathy (Bernard-Soulier) 287.1 constitutional 286.4 Willebrand-Jürgens (angiohemophilia) 286.4