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type
sameAs
notation
  • 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
alternative label
  • Maladie de Moschcowitz
  • Purpura thrombopénique thrombotique
  • Syndrome de Moschcowitz
  • Purpura thrombocytopénique thrombotique
  • Microangiopathy, Familial Thrombotic
  • Moschcowitz Disease
  • Purpura thrombotique thrombocytopénique familial
  • Thrombocytopenic Purpura, Thrombotic
  • Upshaw Factor, Deficiency of
  • Familial Thrombotic Thrombocytopenic Purpura
  • Micro-angiopathie thrombotique thrombocytopénique
  • PTT (Purpura Thrombotique Thrombocytopénique)
  • Purpura, Thrombotic Thrombocytopenic
  • Purpura, Thrombotic Thrombopenic
  • Syndrome d'Upshaw-Schulman
  • Upshaw Schulman Syndrome
  • Familial Thrombotic Thrombocytopenia Purpura
  • Schulman Upshaw Syndrome
  • Schulman-Upshaw Syndrome
  • Thrombotic Microangiopathy, Familial
  • Thrombotic Thrombocytopenic Purpura, Congenital
  • Thrombotic Thrombocytopenic Purpura, Familial
  • Thrombotic Thrombopenic Purpura
  • Purpura thrombotique thrombocytopénique congénital
  • Congenital Thrombotic Thrombocytopenic Purpura
  • Familial Thrombotic Microangiopathy
  • Microangiopathic Hemolytic Anemia, Congenital
  • Microangiopathie thrombotique thrombocytopénique
  • Moschkowitz Disease
  • Thrombotic Thrombocytopenic Purpura
  • Upshaw-Schulman Syndrome
  • Thrombopenic Purpura, Thrombotic
preferred label
  • Purpura thrombotique thrombocytopénique
is in scheme
note
  • 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. Mutations in the ADAMTS13 PROTEIN gene have been identified in familial cases
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is Subject of
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