icd 10 code for fibrinogen deficiency

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What is the ICD 10 code for vitamin deficiency?

Deficiency of other specified B group vitamins 1 E53.8 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. 2 The 2020 edition of ICD-10-CM E53.8 became effective on October 1, 2019. 3 This is the American ICD-10-CM version of E53.8 - other international versions of ICD-10 E53.8 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 coagulation defect?

Other specified coagulation defects. D68.8 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 fibrinogen?

Hereditary deficiency of other clotting factors The 2022 edition of ICD-10-CM D68. 2 became effective on October 1, 2021. This is the American ICD-10-CM version of D68.

What is the ICD-10 code for clotting disorder?

ICD-10 code D68. 9 for Coagulation defect, unspecified 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 factor2 deficiency?

Hypoprothrombinemia; Factor II deficiency; Dysprothrombinemia. Prothrombin deficiency is a disorder caused by a lack of a protein in the blood called prothrombin. It leads to problems with blood clotting (coagulation). Prothrombin is also known as factor II (factor two).

What ICD-10 codes cover Factor V Leiden?

Factor v leiden mutation (r506q) is the most common cause of apc resistance. An abnormality that refers to mutation of factor v leiden, which is a variant of human factor v. It results in thrombophilia, deep vein thrombosis, and a slightly increased risk of miscarriage.

What is ICD-10 code for factor VII deficiency?

D68. 2 - Hereditary deficiency of other clotting factors. ICD-10-CM.

What is the ICD-10 code for protein S deficiency?

D53. 0 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.

What is fibrinogen?

Listen to pronunciation. (fy-BRIH-noh-jen) A protein involved in forming blood clots in the body. It is made in the liver and forms fibrin.

What is Parahemophilia?

Factor V deficiency is also known as Owren's disease or parahemophilia. It's a rare bleeding disorder that results in poor clotting after an injury or surgery. Factor V deficiency shouldn't be confused with factor V Leiden mutation, a much more common condition that causes excessive blood clotting.

What is Trombofilia?

Thrombophilia is a condition that increases your risk of blood clots. It's usually treated with anticoagulant medicines.

What is Leiden?

Overview. Factor V Leiden (FAK-tur five LIDE-n) is a mutation of one of the clotting factors in the blood. This mutation can increase your chance of developing abnormal blood clots, most commonly in your legs or lungs. Most people with factor V Leiden never develop abnormal clots.

What is heterozygous factor V Leiden?

Factor V Leiden is an inherited disorder that makes blood more likely to clot. If you have this disorder you are at risk of developing blood clots, especially in your leg veins. Most people with this disorder have no problems.

Is Factor V Leiden covered by Medicare?

This testing is considered investigational and is NOT a Medicare benefit.