icd 10 code for factor 2 dna mutation

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What is the ICD 10 code for genetic diagnosis?

ICD-10-CM Diagnosis Code Z15.89 ICD-10-CM Diagnosis Code Z15.09 Susceptibility to disease, genetic Z15.89 ICD-10-CM Diagnosis Code Z15.89 ICD-10-CM Diagnosis Code Z15.09 Li-Fraumeni Z15.01 ICD-10-CM Codes Adjacent To Z15.01 Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.

What is the ICD 10 code for prothrombin mutation?

2018/2019 ICD-10-CM Diagnosis Code D68.52. Prothrombin gene mutation. 2016 2017 2018 2019 Billable/Specific Code. D68.52 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 hereditary deficiency of other clotting?

2018/2019 ICD-10-CM Diagnosis Code D68.2. Hereditary deficiency of other clotting factors. 2016 2017 2018 2019 Billable/Specific Code. 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 genetic susceptibility to neoplasm?

Genetic susceptibility to malignant neoplasm of breast. Z15.01 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 Z15.01 became effective on October 1, 2018.

What is a factor 2 mutation?

Prothrombin gene mutation (or Factor II mutation or Prothrombin G20210A) is an inherited condition that increases your predisposition to develop abnormal blood clots in the veins (deep vein thrombosis or DVT) and lungs (pulmonary embolism or PE).

What Is factor II DNA analysis?

This test measures how much of a protein called factor II is in your blood. Factor II is also called prothrombin. This test can help find out whether you have a bleeding or blood clotting disorder.

What is the ICD-10 code for brca2 gene mutation positive?

BRCA1 and/or 2 positive results are assigned either ICD-10-CM code Z15. 01 Genetic susceptibility to malignant neoplasm of breast or Z15. 02 Genetic susceptibility to malignant neoplasm of ovary, depending on family history.

How common is factor II mutation?

A change in the prothrombin gene is present in 2-4% (or 1 in 50 to 1 in 25) of Caucasians, and is more common in individuals of European ancestry. In the United States, approximately 0.4% (about 1 in 250) of African Americans also have the mutation.

What's the difference between factor 2 and Factor 5?

The Factor V variant known as Factor V Leiden (or rs6025) is associated with an approximately 300% increased risk in heterozygotes and an up to 8000% increased risk in homozygotes. The Factor II rs1799963 polymorphism (or G20210A) may also independently increase the risk by approximately 200%.

How is factor 2 diagnosed?

Diagnosis of factor II deficiency is based on your medical history, any family history of bleeding problems, and lab tests. Lab tests for bleeding disorders include: Factor assays: These tests check the performance of specific factors to identify missing or poorly performing factors.

What is the ICD-10 code for gene mutation?

Chromosomal abnormality, unspecified Q99. 9 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 Q99. 9 became effective on October 1, 2021.

What is code Z12 39?

39 (Encounter for other screening for malignant neoplasm of breast). Z12. 39 is the correct code to use when employing any other breast cancer screening technique (besides mammogram) and is generally used with breast MRIs.

What does HER2/neu negative mean?

Listen to pronunciation. (… NEH-guh-tiv) Describes cells that have a small amount or none of a protein called HER2 on their surface.

How many people in the world have factor 2?

The incidence is estimated at 1 in 2 million in the general population.

Where is factor 2 produced?

Factor II (prothrombin): Synthesized in the liver; becomes active only after carboxylation by vitamin K. It is converted to thrombin (factor IIa).

What is a factor 2 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).