icd 10 code for factor v deficiency

What is the ICD 10 code for coagulation factor deficiency?

ICD-10-CM Diagnosis Code D68.1 [convert to ICD-9-CM] Hereditary factor XI deficiency. Factor xi deficiency, type i; Hemophilia c; Hemophilia c, type 1; Hereditary factor xi deficiency disease; Hemophilia C; Plasma thromboplastin antecedent [PTA] deficiency; Rosenthal's disease. ICD-10-CM Diagnosis Code D68.1.

What is the ICD 10 code for factor V Leiden mutation?

Vitamin B12 defic anemia due to intrinsic factor deficiency; Anemia, pernicious; Pernicious anemia; Addison anemia; Biermer anemia; Pernicious (congenital) anemia; Congenital intrinsic factor deficiency. ICD-10-CM Diagnosis Code D51.0. Vitamin B12 deficiency anemia due to intrinsic factor deficiency.

What is factor V deficiency?

ICD-10-CM Diagnosis Code I69.31 Cognitive deficits following cerebral infarction 2016 2017 - Converted to Parent Code 2018 2019 2020 2021 2022 Non-Billable/Non-Specific Code

What is the ICD 10 code for heredity deficiency?

Nov 29, 2021 · Clinical test for Factor V deficiency offered by Diagenom GmbH

What diagnosis code will cover factor v leiden?

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 ICD 10 code for Factor XI deficiency?

Table: CodeICD10 Code (*)Code Description (*)D68.1Hereditary factor XI deficiencyD68.2Hereditary deficiency of other clotting factorsD68.3Haemorrhagic disorder due to circulating anticoagulantsD68.4Acquired coagulation factor deficiency4 more rows

What is acquired coagulation deficiency?

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.Mar 24, 2017

What is diagnosis code K920?

HematemesisK920 - ICD 10 Diagnosis Code - Hematemesis - Market Size, Prevalence, Incidence, Quality Outcomes, Top Hospitals & Physicians.

What is hereditary factor VIII deficiency?

Hemophilia A, also called factor VIII (8) deficiency or classic hemophilia, is a genetic disorder caused by missing or defective factor VIII (FVIII), a clotting protein. Although it is passed down from parents to children, about 1/3 of cases found have no previous family history.

What is ICD 10 code for hemophilia A?

Z14. 02 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.

What is factor VII deficiency?

Factor VII (seven) deficiency is a disorder caused by a lack of a protein called factor VII in the blood. It leads to problems with blood clotting (coagulation). Blood clotting normally occurs when there is damage to a blood vessel.

What is factor XIII deficiency?

Factor XIII deficiency is a rare bleeding disorder. Researchers have identified an inherited form and a less severe form that is acquired during a person's lifetime. Signs and symptoms of inherited factor XIII deficiency begin soon after birth, usually with abnormal bleeding from the umbilical cord stump.

What are the coagulation disorders?

Coagulations disorders are conditions that affect the blood's clotting activities. Hemophilia, Von Willebrand disease, clotting factor deficiencies, hypercoagulable states and deep venous thrombosis are all coagulations disorders. Hemophilia and Von Willebrand disease are among the best known.

What is the ICD-10 DX code for hematemesis?

K92.0K92. 0 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.

What is the correct ICD-10 code for thrombocytopenia?

ICD-10 | Thrombocytopenia, unspecified (D69. 6)

What is hematemesis evidence?

Melena strongly suggests, and hematemesis confirms, that bleeding is of upper gastrointestinal origin. In this situation, seek historical evidence for common causes such as peptic ulcer, cirrhosis with esophageal or gastric varices, gastritis, esophagitis, Mallory–Weiss tears, and malignancy.

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.