Idiopathic thrombocytopenic purpura (ITP): Difference between revisions
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| OldDxArticle =ITP| CurrentStatus = | | OldDxArticle =ITP| CurrentStatus = reconciled | ||
| InitialEditorAssigned = Elaine Nagy | | InitialEditorAssigned = Elaine Nagy | ||
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{{ICD10 dx | {{ICD10 dx | ||
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| ICD10 Code=D69.3 | | ICD10 Code=D69.3 | ||
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{{ICD10 category|Heme/immunology}}{{ICD10 category|Thrombocytopenia}} | |||
== Additional Info == | == Additional Info == | ||
Idiopathic thrombocytopenic purpura (ITP) is a bleeding disorder in which the immune system destroys platelets, which are necessary for normal blood clotting. People with the disease have too few platelets in the blood. ITP is sometimes called immune thrombocytopenic purpura or simply, immune thrombocytopenia | |||
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{{ListICD10Category | categoryName = Thrombocytopenia}} | |||
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== Related Articles == | == Related Articles == | ||
{{Related Articles}} | {{Related Articles}} | ||
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