Purpura, Thrombocytopenic, Idiopathic D016553

Related MeSH Hierarchy (7)

Diseases [C] » Hemic and Lymphatic Diseases [C15] » Hematologic Diseases » Blood Coagulation Disorders » Purpura » Purpura, Thrombocytopenic » Purpura, Thrombocytopenic, Idiopathic

Diseases [C] » Hemic and Lymphatic Diseases [C15] » Hematologic Diseases » Hemorrhagic Disorders » Purpura, Thrombocytopenic, Idiopathic

Diseases [C] » Immune System Diseases [C20] » Autoimmune Diseases » Purpura, Thrombocytopenic, Idiopathic

Diseases [C] » Immune System Diseases [C20] » Purpura, Thrombocytopenic » Purpura, Thrombocytopenic, Idiopathic

Diseases [C] » Pathological Conditions, Signs and Symptoms [C23] » Pathologic Processes » Hemorrhage » Purpura » Purpura, Thrombocytopenic » Purpura, Thrombocytopenic, Idiopathic

Diseases [C] » Pathological Conditions, Signs and Symptoms [C23] » Signs and Symptoms » Skin Manifestations » Purpura » Purpura, Thrombocytopenic » Purpura, Thrombocytopenic, Idiopathic

Description

Thrombocytopenia occurring in the absence of toxic exposure or a disease associated with decreased platelets. It is mediated by immune mechanisms, in most cases IMMUNOGLOBULIN G autoantibodies which attach to platelets and subsequently undergo destruction by macrophages. The disease is seen in acute (affecting children) and chronic (adult) forms.   MeSH


Organization Involved with Phase 3 Indications (107)

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