2024 ICD-10-CM Diagnosis Code D68.4

Approximate Synonyms

The following clinical terms are approximate synonyms or lay terms that might be used to identify the correct diagnosis code:

• Acquired coagulation factor deficiency
• Acquired combined coagulation factor deficiency
• Acquired factor II deficiency
• Acquired factor IX deficiency disease
• Acquired factor V deficiency disease
• Acquired factor VII deficiency disease
• Acquired factor VIII deficiency disease
• Acquired factor X deficiency disease
• Acquired factor XI deficiency disease
• Acquired factor XII deficiency disease
• Acquired factor XIII deficiency disease
• Acquired hemophilia
• Acquired prekallikrein deficiency
• Autoimmune factor VIII deficiency
• Blood coagulation disorder due to liver disease
• Deficiency of coagulation factor due to liver disease
• Deficiency of coagulation factor due to vitamin K deficiency
• Deficiency of coagulation factor due to vitamin K deficiency
• Deficiency of coagulation factor due to vitamin K deficiency
• Deficiency of coagulation factor due to vitamin K malabsorption in obstructive biliary disease
• Factor II deficiency
• Factor V deficiency
• Factor VII deficiency
• Factor X deficiency
• Factor X deficiency
• Factor X deficiency due to systemic amyloidosis
• Factor XI deficiency
• Factor XII deficiency disease
• Factor XIII deficiency disease
• Idiopathic factor VIII deficiency
• Malignancy-related factor VIII deficiency
• Prekallikrein deficiency
• Prothrombin complex deficiency
• Prothrombin complex deficiency
• Prothrombin complex deficiency
• Prothrombin complex deficiency
• Vitamin K deficiency
• Vitamin K deficiency coagulation disorder
• Vitamin K deficiency coagulation disorder due to malabsorption
• Vitamin K deficiency coagulation disorder due to malabsorption

Clinical Information

• Factor VII Deficiency

  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.

• Factor V Deficiency

  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)

• Vitamin K Deficiency

  a nutritional condition produced by a deficiency of vitamin k in the diet, characterized by an increased tendency to hemorrhage (hemorrhagic disorders). such bleeding episodes may be particularly severe in newborn infants. (from cecil textbook of medicine, 19th ed, p1182)

• Vitamin K Deficiency Bleeding

  hemorrhage caused by vitamin k deficiency.

• Factor X Deficiency

  blood coagulation disorder usually inherited as an autosomal recessive trait, though it can be acquired. it is characterized by defective activity in both the intrinsic and extrinsic pathways, impaired thromboplastin time, and impaired prothrombin consumption.

• Factor XI Deficiency

  a hereditary deficiency of blood coagulation factor xi (also known as plasma thromboplastin antecedent or pta or antihemophilic factor c) resulting in a systemic blood-clotting defect called hemophilia c or rosenthal's syndrome, that may resemble classical hemophilia.

• Acquired Factor II Deficiency

  an acquired coagulation disorder characterized by the partial or complete absence of prothrombin (factor ii) activity in the blood.

• Acquired Factor VII Deficiency

  an acquired coagulation disorder characterized by the partial or complete absence of factor vii activity in the blood.

• Factor VII Deficiency

  a coagulation disorder characterized by the partial or complete absence of factor vii activity in the blood.

• Hereditary Factor VII Deficiency

  a rare autosomal recessive inherited blood coagulation disorder characterized by deficiency of factor vii, resulting in bleeding.

• Acquired Factor V Deficiency

  an acquired coagulation disorder characterized by the partial or complete absence of factor v activity in the blood.

• Factor V Deficiency

  a coagulation disorder characterized by the partial or complete absence of factor v activity in the blood.

• Hereditary Factor V Deficiency|Owren Disease

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

• Prekallikrein Deficiency

  a condition characterized by the congenital or acquired deficiency of prekallikrein. this deficiency is usually not associated with bleeding. the congenital deficiency is very rare. acquired deficiency may occur in diffuse intravascular coagulation, infections, and sickle cell disease.

• Factor II Deficiency

  a coagulation disorder characterized by the partial or complete absence of prothrombin (factor ii) activity in the blood.

• Hereditary Factor II Deficiency|Hereditary Hypoprothrombinemia|Hereditary Prothrombin Deficiency

  a very rare autosomal recessive inherited blood coagulation disorder characterized by deficiency of prothrombin, resulting in bleeding.

• Acquired Factor X Deficiency

  an acquired coagulation disorder characterized by the partial or complete absence of factor x activity in the blood.

• Factor X Deficiency

  a coagulation disorder characterized by the partial or complete absence of factor x activity in the blood.

• Hereditary Factor X Deficiency|Stuart-Prower Factor Deficiency

  a rare autosomal recessive inherited blood coagulation disorder characterized by deficiency of factor x, resulting in bleeding.

• Acquired Factor XI Deficiency

  an acquired coagulation disorder characterized by the partial or complete absence of factor xi activity in the blood.

• Factor XI Deficiency

  a coagulation disorder characterized by the partial or complete absence of factor xi activity in the blood.

• Hereditary Factor XI Deficiency|Hemophilia C|Hereditary Factor XI Deficiency Disease|Hereditary Factor XI Deficiency Disease|Hereditary factor XI deficiency

  a rare inherited bleeding disorder caused by deficiency of coagulation factor xi. it may be asymptomatic or manifest with bleeding.

Convert D68.4 to ICD-9-CM

• ICD-9-CM Code: 286.7 - Acq coagul factor defic
  Approximate Flag - The approximate mapping means there is not an exact match between the ICD-10 and ICD-9 codes and the mapped code is not a precise representation of the original code.

Patient Education

Bleeding Disorders

Normally, if you get hurt, your body forms a blood clot to stop the bleeding. For blood to clot, your body needs cells called platelets and proteins known as clotting factors. If you have a bleeding disorder, you either do not have enough platelets or clotting factors or they don't work the way they should.

Bleeding disorders can be the result of other diseases, such as severe liver disease or a lack of vitamin K. They can also be inherited. Hemophilia is an inherited bleeding disorder. Bleeding disorders can also be a side effect of medicines such as blood thinners.

Various blood tests can check for a bleeding disorder. You will also have a physical exam and history. Treatments depend on the cause. They may include medicines and transfusions of blood, platelets, or clotting factor.

Code History

• FY 2024 - No Change, effective from 10/1/2023 through 9/30/2024
• FY 2023 - No Change, effective from 10/1/2022 through 9/30/2023
• FY 2022 - No Change, effective from 10/1/2021 through 9/30/2022
• FY 2021 - No Change, effective from 10/1/2020 through 9/30/2021
• FY 2020 - No Change, effective from 10/1/2019 through 9/30/2020
• FY 2019 - No Change, effective from 10/1/2018 through 9/30/2019
• FY 2018 - No Change, effective from 10/1/2017 through 9/30/2018
• FY 2017 - No Change, effective from 10/1/2016 through 9/30/2017
• FY 2016 - New Code, effective from 10/1/2015 through 9/30/2016. This was the first year ICD-10-CM was implemented into the HIPAA code set.