hemophilia C (Q1393718)

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human disease
  • Congenital factor XI deficiency
  • Hereditary factor XI deficiency disease (disorder)
  • Rosenthal's disease
  • plasma thromboplastin antecedent deficiency
  • Hereditary factor XI deficiency disease
  • haemophilia C
  • Pta Deficiency
  • Hereditary Factor XI Deficiency
  • Rosenthal Syndrome
  • Rosenthal factor deficiency
  • FACTOR XI DEFICIENCY
  • F11 Deficiency
  • factor XI deficiency
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Language Label Description Also known as
English
hemophilia C
human disease
  • Congenital factor XI deficiency
  • Hereditary factor XI deficiency disease (disorder)
  • Rosenthal's disease
  • plasma thromboplastin antecedent deficiency
  • Hereditary factor XI deficiency disease
  • haemophilia C
  • Pta Deficiency
  • Hereditary Factor XI Deficiency
  • Rosenthal Syndrome
  • Rosenthal factor deficiency
  • FACTOR XI DEFICIENCY
  • F11 Deficiency
  • factor XI deficiency

Statements

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Identifiers

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3B13
Haemophilia C
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