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).
Z83. 2 - Family history of diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism | ICD-10-CM.
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 .
D68. 51 - Activated protein C resistance | ICD-10-CM.
Acquired coagulation factor deficiency D68. 4 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. 4 became effective on October 1, 2021.
Factor V deficiency is caused by a lack of factor V. When certain blood clotting factors are low or missing, your blood does not clot properly. Factor V deficiency is rare. It may be caused by: A defective factor V gene passed down through families (inherited)
ICD-10-CM classifies acute blood loss anemia to code D62, Acute posthemorrhagic anemia, and chronic blood loss anemia to code D50. 0, Iron deficiency anemia secondary to blood loss (chronic). An Excludes1 note for “anemia due to chronic blood loss (D50.
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.
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.
Protein C deficiency is a rare disorder that causes abnormal clotting of your blood. Protein C is one of many natural anticoagulants in blood that helps keep your clotting mechanism in check. An anticoagulant is a substance that prevents blood from clotting.
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.
Inheritance. Protein S deficiency is inherited in an autosomal dominant pattern , which means one altered copy of the PROS1 gene in each cell is sufficient to cause mild protein S deficiency. Individuals who inherit two altered copies of this gene in each cell have severe protein S deficiency.
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.
Hemophilia is usually an inherited bleeding disorder in which the blood does not clot properly. This can lead to spontaneous bleeding as well as bleeding following injuries or surgery. Blood contains many proteins called clotting factors that can help to stop bleeding.
Factor VIII is one of the essential blood proteins and plays a role in aiding the blood to clot in response to injury. Mutations of the F8 gene result in deficient levels of functional factor VIII. The symptoms of hemophilia A occur due to this deficiency. The F8 gene is located on the X chromosome.
ICD-10 code D68. 0 for Von Willebrand's disease 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 .