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D68.2 Hereditary deficiency of other clotting factors

D68.2 Hereditary deficiency of other clotting factors

Owned by Arvind Kuppusamy
Oct 18, 2023

Summary

  • Status: Active
  • Version: 2023
  • ORDER_NO: 03568

Descriptions

  • Proaccelerin deficiency [ ET en ]
  • Owren's disease [ ET en ]
  • AC globulin deficiency [ ET en ]
  • Hypoproconvertinemia [ ET en ]
  • Dysfibrinogenemia (congenital) [ ET en ]
  • Hereditary deficiency of other clotting factors [ PT en ]
  • Hereditary deficiency of other clotting factors [ AB en ]
  • Congenital afibrinogenemia [ ET en ]
  • Deficiency of factor V [labile] [ ET en ]
  • Deficiency of factor VII [stable] [ ET en ]
  • Deficiency of factor X [Stuart-Prower] [ ET en ]
  • Deficiency of factor XII [Hageman] [ ET en ]
  • Deficiency of factor XIII [fibrin stabilizing] [ ET en ]
  • Deficiency of factor II [prothrombin] [ ET en ]
  • Deficiency of factor I [fibrinogen] [ ET en ]

Parent Concepts

  • D68 Other coagulation defects

Child Concepts

None

Defining Attributes

None

Diagram

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