D68.2

Applicable To

• AC globulin deficiency

• Congenital afibrinogenemia

• Deficiency of factor I [fibrinogen]

• Deficiency of factor II [prothrombin]

• Deficiency of factor V [labile]

• Deficiency of factor VII [stable]

• Deficiency of factor X [Stuart-Prower]

• Deficiency of factor XII [Hageman]

• Deficiency of factor XIII [fibrin stabilizing]

• Dysfibrinogenemia congenital)

• Hypoproconvertinemia

• Owren’s disease

• Proaccelerin deficiency

Approximate Synonyms

• Clotting factor deficiency, congenital

• Congenital coagulation factor deficiency

• Dysfibrinogenemia

• Dysfibrinogenemia, congenital

• Factor 10 deficiency

• Factor 12 deficiency

• Factor 2 mutation

• Factor 5 deficiency

• Factor 7 deficiency

• Factor ii deficiency

• Factor v deficiency

• Factor v quebec

• Factor vii deficiency

• Factor x deficiency

• Factor xii deficiency disease

• Hereditary dysfibrinogenemia

• Platelet factor v deficiency factor v quebec)

Clinical Information

• A blood coagulation disorder characterized by the complete absence of fibrinogen in the blood, resulting in bleeding.

• A deficiency of blood coagulation factor v known as proaccelerin or accelerator globulin or labile factor) leading to a rare hemorrhagic tendency known as owren’s disease or parahemophilia. It varies greatly in severity. Factor v deficiency is an autosomal recessive trait. Dorland, 27th ed)

• A deficiency or absence of fibrinogen in the blood.

• A usually inherited blood coagulation disorder characterized by the partial or complete absence of fibrinogen in the blood, resulting in bleeding.

• A very rare autosomal recessive inherited blood coagulation disorder characterized by deficiency of factor v, resulting in bleeding.

• An autosomal recessive characteristic or a coagulation disorder acquired in association with vitamin k deficiency. Factor vii is a vitamin k dependent glycoprotein essential to the extrinsic pathway of coagulation.

• Deficiency or absence of fibrinogen coagulation factor i) in the blood.

Details

• D68.2 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.

• The 2023 edition of ICD-10-CM D68.2 became effective on October 1, 2022.

• This is the American ICD-10-CM version of D68.2 – other international versions of ICD-10 D68.2 may differ.