An acquired, congenital, or familial disorder caused by PLATELET AGGREGATION with THROMBOSIS in terminal arterioles and capillaries. Clinical features include THROMBOCYTOPENIA; HEMOLYTIC ANEMIA; AZOTEMIA; FEVER; and thrombotic microangiopathy. The classical form also includes neurological symptoms and end-organ damage, such as RENAL FAILURE.

Descriptor ID	D011697
MeSH Number(s)	C15.378.100.802.687.680 C15.378.140.855.925.750.680 C15.378.925.850 C23.550.414.950.687.680 C23.888.885.687.687.680
Concept/Terms	Purpura, Thrombotic Thrombocytopenic Purpura, Thrombotic Thrombocytopenic Thrombocytopenic Purpura, Thrombotic Moschkowitz Disease Disease, Moschkowitz Thrombotic Thrombocytopenic Purpura Moschcowitz Disease Disease, Moschcowitz Purpura, Thrombotic Thrombopenic Thrombopenic Purpura, Thrombotic Thrombotic Thrombopenic Purpura Congenital Thrombotic Thrombocytopenic Purpura Congenital Thrombotic Thrombocytopenic Purpura Schulman-Upshaw Syndrome Schulman Upshaw Syndrome Syndrome, Schulman-Upshaw Upshaw-Schulman Syndrome Syndrome, Upshaw-Schulman Upshaw Schulman Syndrome Thrombotic Thrombocytopenic Purpura, Congenital Upshaw Factor, Deficiency of Microangiopathic Hemolytic Anemia, Congenital Thrombotic Microangiopathy, Familial Familial Thrombotic Microangiopathy Microangiopathy, Familial Thrombotic Familial Thrombotic Thrombocytopenic Purpura Familial Thrombotic Thrombocytopenic Purpura Thrombotic Thrombocytopenic Purpura, Familial Familial Thrombotic Thrombocytopenia Purpura

Below are MeSH descriptors whose meaning is more general than "Purpura, Thrombotic Thrombocytopenic".

Below are MeSH descriptors whose meaning is related to "Purpura, Thrombotic Thrombocytopenic".

Below are MeSH descriptors whose meaning is more specific than "Purpura, Thrombotic Thrombocytopenic".