Upshaw Schulman Syndrome (Q18604563)

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medical condition
  • congenital thrombotic thrombocytopenic purpura
  • Congenital ADAMTS13 Deficiency
  • Microangiopathic Hemolytic Anemia, Congenital
  • Upshaw Factor, Deficiency of
  • Thrombotic Thrombocytopenic Purpura, Familial
  • Upshaw-Schulman Syndrome
  • THROMBOTIC THROMBOCYTOPENIC PURPURA, CONGENITAL; TTP
  • Thrombotic Microangiopathy, Familial
  • THROMBOTIC THROMBOCYTOPENIC PURPURA, CONGENITAL
  • Microangiopathic Hemolytic Anemia
  • Congenital TTP
  • Familial TTP
  • Congenital ADAMTS-13 deficiency
  • TTP
  • Schulman-Upshaw Syndrome
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Language Label Description Also known as
English
Upshaw Schulman Syndrome
medical condition
  • congenital thrombotic thrombocytopenic purpura
  • Congenital ADAMTS13 Deficiency
  • Microangiopathic Hemolytic Anemia, Congenital
  • Upshaw Factor, Deficiency of
  • Thrombotic Thrombocytopenic Purpura, Familial
  • Upshaw-Schulman Syndrome
  • THROMBOTIC THROMBOCYTOPENIC PURPURA, CONGENITAL; TTP
  • Thrombotic Microangiopathy, Familial
  • THROMBOTIC THROMBOCYTOPENIC PURPURA, CONGENITAL
  • Microangiopathic Hemolytic Anemia
  • Congenital TTP
  • Familial TTP
  • Congenital ADAMTS-13 deficiency
  • TTP
  • Schulman-Upshaw Syndrome

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