icd 10 code for factor vleiden

by Patrick Gerlach 10 min read

Factor v leiden mutation (r506q) is the most common cause of apc resistance
apc resistance
Activated protein C resistance (APCR) is a hypercoagulability (an increased tendency of the blood to clot) characterized by a lack of a response to activated protein C (APC), which normally helps prevent blood from clotting excessively.
https://en.wikipedia.org › wiki › Activated_protein_C_resistance
. An abnormality that refers to mutation of factor v leiden, which is a variant of human factor v. It results in thrombophilia
thrombophilia
Thrombophilia (sometimes called hypercoagulability or a prothrombotic state) is an abnormality of blood coagulation that increases the risk of thrombosis (blood clots in blood vessels).
https://en.wikipedia.org › wiki › Thrombophilia
, deep vein thrombosis, and a slightly increased risk of miscarriage.

What is the ICD-10 code for family history of factor V Leiden?

Z83. 2 - Family history of diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism | ICD-10-CM.

What is factor V Leiden heterozygous?

Heterozygous means that the 2 copies of a gene are different. In your case, one of your Factor V gene codes is for normal clotting Factor V and the other Factor V gene code is for Factor V Leiden. There is more risk of a blood clot if both gene codes are for Factor V Leiden (ie in the homozygous state).

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 the factor 5 gene?

Factor V Leiden (FVL), or factor “5” Leiden, is a genetic mutation (change) that makes the blood more prone to abnormal clotting. Factor V Leiden is the most common genetic predisposition to blood clots.

What is the difference between Factor V and Factor V Leiden?

Factor V Leiden is a common change in a gene that controls a protein called Factor V. Factor V is a protein involved in blood clotting and the Factor V Leiden gene change (also called mutation) is linked to an increase risk of blood clots.

What are the two types of factor V Leiden?

Having 1 Factor V Leiden gene (heterozygous type) slightly increases the chance of developing a blood clot. Having 2 Factor V Leiden genes (homozygous type) makes the risk much greater. Having Factor V Leiden does not appear to increase the chances of developing a heart attack or stroke.

What ICD-10 covers PT PTT?

NCD - Partial ThromboplastinTime (PTT) (190.16)

What is the ICD-10 code for long term anticoagulation?

01 Long term (current) use of anticoagulants.

When do you code a D68 9?

To assign D68. 9, the provider needs to specifically diagnose and documented by the provider, as well as indicate it is not contributed to a prescribed anticoagulant therapy.

Is factor V Leiden considered a blood disorder?

Factor V Leiden thrombophilia is an inherited disorder of blood clotting .

What is the difference between Factor 5 and factor 2?

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%.

What is the CPT code for clotting factor V?

Group 1CodeDescription81241F5 (COAGULATION FACTOR V) (EG, HEREDITARY HYPERCOAGULABILITY) GENE ANALYSIS, LEIDEN VARIANT81291MTHFR (5,10-METHYLENETETRAHYDROFOLATE REDUCTASE) (EG, HEREDITARY HYPERCOAGULABILITY) GENE ANALYSIS, COMMON VARIANTS (EG, 677T, 1298C)1 more row

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.

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