icd 10 code for factor viii disorder

by Adrian Howell 5 min read

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 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 coagulation factor deficiency?

Acquired coagulation factor deficiency 1 D68.4 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. 2 The 2021 edition of ICD-10-CM D68.4 became effective on October 1, 2020. 3 This is the American ICD-10-CM version of D68.4 - other international versions of ICD-10 D68.4 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 D66?

2016 2017 2018 2019 Billable/Specific Code. D66 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 D66 became effective on October 1, 2018.

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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 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 ICD-10 code for hemophilia A?

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

What Is factor VIII 8 or factor IX 9?

People with hemophilia have low levels of either factor VIII (8) or factor IX (9). The severity of hemophilia that a person has is determined by the amount of factor in the blood. The lower the amount of the factor, the more likely it is that bleeding will occur which can lead to serious health problems.

What is the name of factor VIII?

Factor VIII (antihemophilic factor) is the protein that is deficient or defective in patients with classical hemophilia and Von Willebrand syndrome. Factor VIII in plasma is thought to be associated in a complex with the highest molecular weight multimers of another glycoprotein, Von Willebrand protein.

What causes low factor VIII?

If you have an abnormally low level of factor VIII, it could be caused by: an inherited factor VIII deficiency (hemophilia A) disseminated intravascular coagulation (DIC), a disease in which certain proteins responsible for blood clotting are abnormally active. the presence of a factor VIII inhibitor.

What is factor VII deficiency?

Factor VII (seven) deficiency is a disorder caused by a lack of a protein called factor VII in the blood. It leads to problems with blood clotting (coagulation). Blood clotting normally occurs when there is damage to a blood vessel.

Which disease is also called Christmas disease?

Hemophilia B is the second most common type of hemophilia. 1,2. It is also known as factor IX deficiency, or Christmas disease. It was originally named “Christmas disease” after the first person diagnosed with the disorder back in 1952.

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 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 the diagnosis code for hemophilia?

Group 2CodeDescriptionD68.311Acquired hemophilia

What is the name of the deficiency of fibrinogen in the blood?

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.

What is a blood coagulation disorder?

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.

What is hemophilioid disorder?

Hemophilioid disorder due to deficiency of von willebrand factor and thus of factor viii complex. Hereditary or acquired coagulation disorder characterized by a qualitative or quantitative deficiency of the von willebrand factor. The latter plays an important role in platelet adhesion.

Is the von Willebrand factor autosomal dominant?

Clinical Information. Group of hemorrhagic disorders in which the von willebrand factor is either quantitatively or qualitatively abnormal. They are usually inherited as an autosomal dominant trait though rare kindreds are autosomal recessive.

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