icd 10 code for factor viii overactivity

What is the ICD 10 code for factor VIII deficiency?

Hereditary factor VIII deficiency 1 D66 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. 2 The 2019 edition of ICD-10-CM D66 became effective on October 1, 2018. 3 This is the American ICD-10-CM version of D66 - other international versions of ICD-10 D66 may differ.

What is the ICD 10 code for overactivity?

Overactivity. R46.3 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2018/2019 edition of ICD-10-CM R46.3 became effective on October 1, 2018. This is the American ICD-10-CM version of R46.3 - other international versions of ICD-10 R46.3 may differ.

What is the ICD 10 code for heredity deficiency?

Hereditary deficiency of other clotting factors. D68.2 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2019 edition of ICD-10-CM D68.2 became effective on October 1, 2018. This is the American ICD-10-CM version of D68.2 - other international versions of ICD-10 D68.2 may differ.

What is the ICD 10 code for clotting factor deficiency?

Hereditary deficiency of other clotting factors. D68.2 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.

What is the ICD-10 code for elevated factor VIII?

D66 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2022 edition of ICD-10-CM D66 became effective on October 1, 2021. This is the American ICD-10-CM version of D66 - other international versions of ICD-10 D66 may differ.

What is ICD-10 code D66?

ICD-10 code D66 for Hereditary factor VIII deficiency is a medical classification as listed by WHO under the range - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism .

What is ICD-10 code for hemophilia A?

D68. 311 - Acquired hemophilia | ICD-10-CM.

What is the code for hemophilia?

Group 2CodeDescriptionD68.311Acquired hemophilia

What causes elevated factor VIII levels?

Factor VIII levels can be elevated in a number of clinical conditions including carcinoma, leukemia, liver disease, renal disease, hemolytic anemia, diabetes mellitus, deep vein thrombosis, and myocardial infarction.

What is hemophilia Factor 8?

Hemophilia A, also called factor VIII (8) deficiency or classic hemophilia, is a genetic disorder caused by missing or defective factor VIII (FVIII), a clotting protein. Although it is passed down from parents to children, about 1/3 of cases found have no previous family history.

What is acquired VIII deficiency?

Acquired factor VIII deficiency is a bleeding disorder that requires prompt diagnosis and management to avert severe, life-threatening bleeding and death. Despite knowledge of this disorder of coagulation for several decades, relatively little is still known about this disease because of its rare incidence.

What is the ICD 10 code for hemophilia C?

D68. 311 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2022 edition of ICD-10-CM D68. 311 became effective on October 1, 2021.

What is Haemophilia B?

Hemophilia B is a hereditary bleeding disorder caused by a lack of blood clotting factor IX. Without enough factor IX, the blood cannot clot properly to control bleeding.

Which factor is missing in hemophilia A?

In hemophilia, a blood clotting factor is missing. In Hemophilia A, Factor VIII (8) is missing.

What Acquired Hemophilia?

Acquired hemophilia (AH) is a rare autoimmune disorder characterized by bleeding that occurs in patients with no personal or family history of diseases related to clotting/coagulation. Autoimmune disorders occur when the body's immune system mistakenly attacks healthy cells or tissue.

Is Hemophilia homozygous or heterozygous?

The disease is inherited as an X-linked recessive trait and thus occurs in males and very rarely in homozygous females. Heterozygous females for the disease are known as carriers.

How is factor VIII activity determined?

Factor VIII activity is determined utilizing an aPTT-based one-stage clotting time assay . Factor VIII-depleted plasma is used as the substrate and the clotting time with the patient plasma is compared to the clotting time of normal pooled plasma.

Where is factor VIII produced?

Factor VIII is a large glycoprotein cofactor (320 kilodaltons) that is produced mainly in hepatocytes, but also to some extent by liver macrophages, megakaryocytes, and endothelial cells. 6,10 Factor VIII circulates in the plasma bound to von Willebrand factor (vWF) at a concentration of approximately 0.1 mg/mL. 10 The plasma half-life of factor VIII is short at about 8 to 10 hours. 10 Factor VIII deficiency should be suspected when a patient with excessive bleeding has a normal protime (PT) and an extended activated partial thromboplastin time (aPTT).

Can lupus cause low factor VIII?

A lupus anticoagulant may cause factor VIII activity to appear spuriously low and a chromogenic factor VIII activity is recommended in this circumstance.