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D68.2 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 D68.2 became effective on October 1, 2021. … Factor v deficiency is an autosomal recessive trait. (Dorland, 27th ed) A deficiency or absence of fibrinogen in the blood. A usually inherited blood coagulation disorder …
FAQ icd 10 code for factor v deficiency
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 factor V Leiden mutation?
Factor V Leiden mutation. ICD-10-CM Diagnosis Code D68.2 [convert to ICD-9-CM] Hereditary deficiency of other clotting factors. Clotting factor deficiency, congenital; Congenital coagulation factor deficiency; Dysfibrinogenemia; Dysfibrinogenemia, congenital; Factor 10 deficiency; Factor 12 deficiency; Factor 2 mutation; Factor 5 deficiency;
What is the pathophysiology of factor V deficiency?
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. It varies greatly in severity. Factor v deficiency is an autosomal recessive trait. (Dorland, 27th ed)
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.
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| Factor V Leiden (Medical Condition)An inherited disorder of blood clotting. It causes abnormal blood clot in the leg or lungs. |