2024 ICD-10-CM Diagnosis Code D68.2

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 inhibitor disorder
• Alpha chain defect dysfibrinogenemia
• Autosomal dominant deficiency of plasminogen
• Beta chain defect dysfibrinogenemia
• Combined deficiency of factor V and factor VIII
• Congenital afibrinogenemia
• Congenital fibrinogen abnormality
• Congenital plasminogen activator inhibitor deficiency type 1
• Contact factor deficiency
• Drug-induced coagulation inhibitor disorder
• Dysfibrinogenemia
• Dysplasminogenemia
• Factor I deficiency
• Factor I deficiency
• Factor I deficiency disease
• Factor II deficiency
• Factor V deficiency
• Factor V deficiency
• Factor VII deficiency
• Factor X deficiency
• Factor XII deficiency disease
• Factor XIII deficiency disease
• Factor XIII inhibitor disorder
• Fibrinogen abnormality
• Fibrinogen deficiency
• Fibrinogen in blood above reference range
• Fibrinolytic bleeding syndrome
• Gamma chain defect dysfibrinogenemia
• Hemorrhagic disease of the newborn due to factor II deficiency
• Heparin cofactor II deficiency
• Hereditary combined coagulation factor deficiency
• Hereditary combined coagulation factor deficiency
• Hereditary combined deficiency of vitamin K-dependent clotting factors
• Hereditary congenital prekallikrein deficiency
• Hereditary dysfibrinogenemia
• Hereditary dysplasminogenemia
• Hereditary factor I deficiency disease
• Hereditary factor II deficiency disease
• Hereditary factor V deficiency disease
• Hereditary factor VII deficiency disease
• Hereditary factor X deficiency disease
• Hereditary factor XII deficiency disease
• Hereditary factor XIII A subunit and B subunit deficiency
• Hereditary factor XIII A subunit deficiency
• Hereditary factor XIII B subunit deficiency
• Hereditary factor XIII deficiency disease
• Hereditary hypoplasminogenemia
• Hereditary thrombophilic dysfibrinogenemia
• High molecular weight kininogen deficiency
• Hyperfibrinogenemia
• Hypodysfibrinogenemia
• Hypoplasminogenemia
• Immunodeficiency with factor I anomaly
• Neonatal coagulation disorder
• Passovoy factor deficiency
• Platelet factor V deficiency
• Platelet procoagulant activity deficiency
• Prekallikrein deficiency
• Prothrombin complex deficiency

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)

• 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.

• Dysfibrinogenemia

  a coagulation disorder caused by abnormalities in fibrin that result in defective clot formation. this disorder may be inherited or acquired.

• High Molecular Weight Kininogen Deficiency

  a rare autosomal recessive inherited disorder characterized by prolonged partial thromboplastin time and absence of bleeding diathesis.

• 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.

• Acquired Factor II Deficiency

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

• 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.

Convert D68.2 to ICD-9-CM

• ICD-9-CM Code: 286.3 - Cong def clot factor NEC

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.

[Learn More in MedlinePlus]

Factor X deficiency

Factor X deficiency is a rare bleeding disorder that varies in severity among affected individuals. The signs and symptoms of this condition can begin at any age, although the most severe cases are apparent in childhood. Factor X deficiency commonly causes nosebleeds, easy bruising, bleeding under the skin, bleeding of the gums, blood in the urine (hematuria), and prolonged or excessive bleeding following surgery or trauma. Women with factor X deficiency can have heavy or prolonged menstrual bleeding (menorrhagia) or excessive bleeding in childbirth, and may be at increased risk of pregnancy loss (miscarriage). Bleeding into joint spaces (hemarthrosis) occasionally occurs. Severely affected individuals have an increased risk of bleeding inside the skull (intracranial hemorrhage), in the lungs (pulmonary hemorrhage), or in the gastrointestinal tract, which can be life-threatening.

[Learn More in MedlinePlus]

Prothrombin deficiency

Prothrombin deficiency is a bleeding disorder that slows the blood clotting process. People with this condition often experience prolonged bleeding following an injury, surgery, or having a tooth pulled. In severe cases of prothrombin deficiency, heavy bleeding occurs after minor trauma or even in the absence of injury (spontaneous bleeding). Women with prothrombin deficiency can have prolonged and sometimes abnormally heavy menstrual bleeding. Serious complications can result from bleeding into the joints, muscles, brain, or other internal organs. Milder forms of prothrombin deficiency do not involve spontaneous bleeding, and the condition may only become apparent following surgery or a serious injury.

[Learn More in MedlinePlus]

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.