hypoprothrombinemia (Q3801629)

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Human disease
  • Factor 2 deficiency
  • Dysprothrombinemia
  • prothrombin deficiency
  • PROTHROMBIN DEFICIENCY, CONGENITAL
  • Factor II deficiency
  • Congenital factor II deficiency
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Language Label Description Also known as
English
hypoprothrombinemia
Human disease
  • Factor 2 deficiency
  • Dysprothrombinemia
  • prothrombin deficiency
  • PROTHROMBIN DEFICIENCY, CONGENITAL
  • Factor II deficiency
  • Congenital factor II deficiency

Statements

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C26799
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Identifiers

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