icd 10 code for factor thrombocytopenic disorder

What is the ICD 10 code for thrombocytopenia?

Thrombocytopenia, unspecified. D69.6 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2020 edition of ICD-10-CM D69.6 became effective on October 1, 2019.

What is the ICD 10 code for thrombophilia?

Diagnosis Index entries containing back-references to D68.69: Hypercoagulable (state) D68.59 ICD-10-CM Diagnosis Code D68.59. Other primary thrombophilia 2016 2017 2018 2019 Billable/Specific Code Thrombophilia D68.59 ICD-10-CM Diagnosis Code D68.59. Other primary thrombophilia 2016 2017 2018 2019 Billable/Specific Code

What is the ICD 10 code for thrombotic microangiopathy?

Thrombotic microangiopathy. M31.1 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 coagulation defects?

Z86.2 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. This is the American ICD-10-CM version of Z86.2 - other international versions of ICD-10 Z86.2 may differ. D60-D64 Aplastic and other anemias and other bon... D65-D69 Coagulation defects, purpura and other h...

What is the ICD-10 code for thrombocytopenic disorder?

ICD-10 code D69. 6 for Thrombocytopenia, 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 thrombocytopenia unspecified mean?

Thrombocytopenia is a condition in which you have a low blood platelet count. Platelets (thrombocytes) are colorless blood cells that help blood clot. Platelets stop bleeding by clumping and forming plugs in blood vessel injuries.

How do you code autoimmune thrombocytopenia?

ICD-10 Code for Immune thrombocytopenic purpura- D69. 3- Codify by AAPC.

What is the ICD-10 code for personal history of thrombocytopenia?

Z86. 2 - Personal history of diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism | ICD-10-CM.

What are the different types of thrombocytopenia?

The three main classes of thrombocytopenia are:Platelet destruction such as with an auto-antibody that attaches to the platelet surface.Platelet sequestration such as in someone with a large spleen or with liver disease.Decreased platelet production as occurs in certain bone marrow diseases.

What platelet count is thrombocytopenia?

A normal platelet count ranges from 150,000 to 450,000 platelets per microliter of blood. Having more than 450,000 platelets is a condition called thrombocytosis; having less than 150,000 is known as thrombocytopenia.

What is the ICD-10 code for idiopathic thrombocytopenic purpura?

ICD-10 code: D69. 3 Idiopathic thrombocytopenic purpura.

What is the difference between primary and secondary thrombocytopenia?

The ITP Syndrome ITP is an autoimmune bleeding disorder caused by various etiologies, which is characterized by increased platelet destruction and impaired production, resulting in a decreased platelet count. Primary ITP is idiopathic, whereas secondary ITP is linked to an underlying condition (1).

What is considered severe thrombocytopenia?

Degrees of thrombocytopenia can be further subdivided into mild (platelet count 100,000 to 150,000/microL), moderate (50,000 to 99,000/microL), and severe (<50,000/microL) [1].

What is the ICD-10 code for Factor 5?

Factor v leiden mutation (r506q) is the most common cause of apc resistance. An abnormality that refers to mutation of factor v leiden, which is a variant of human factor v. It results in thrombophilia, deep vein thrombosis, and a slightly increased risk of miscarriage.

What is the ICD-10 code for Hypoalbuminemia?

R77. 0 - Abnormality of albumin | ICD-10-CM.

What is ICD-10 code for History of anemia?

V18. 2 - Family history of anemia. ICD-10-CM.

What happens if you have thrombocytopenia?

If you have thrombocytopenia, you don't have enough platelets in your blood. Platelets help your blood clot, which stops bleeding. For most people, it's not a big problem. But if you have a severe form, you can bleed spontaneously in your eyes, gums, or bladder or bleed too much when you're injured.

How do you fix thrombocytopenia?

If your thrombocytopenia is caused by an underlying condition or a medication, addressing that cause might cure it. For example, if you have heparin-induced thrombocytopenia, your doctor can prescribe a different blood-thinning drug....TreatmentBlood or platelet transfusions. ... Medications. ... Surgery. ... Plasma exchange.

What causes your platelets to be low?

A low platelet count can be a result of the body destroying too many platelets too quickly. Some reasons a body might destroy its platelets include : side effects of certain medications, including diuretics, some antibiotics, blood thinners, and anti-seizure medications. an enlarged spleen.

What cancers cause low platelets?

Certain cancers such as leukemia or lymphoma can lower your platelet count. The abnormal cells in these cancers can crowd out healthy cells in the bone marrow, where platelets are made. Less common causes of a low platelet count include: Cancer that spreads to the bone.

What is thrombocytopenia in blood?

Clinical Information. A condition in which there is a lower-than-normal number of platelets in the blood. It may result in easy bruising and excessive bleeding from wounds or bleeding in mucous membranes and other tissues.

What does it mean when blood platelets are decreased?

A decrease in the number of platelets in the blood that may result in easy bruising and excessive bleeding from wound s or bleeding in mucous membranes and other tissues. A finding based on laboratory test results that indicate a decrease in number of platelets in a blood specimen. A subnormal level of blood platelets.

What are the two most common diseases that result in thrombosis in microvasculature?

Diseases that result in thrombosis in microvasculature. The two most prominent diseases are purpura, thrombotic thrombocytopenic; and hemolytic-uremic syndrome. Multiple etiological factors include vascular endothelial cell damage due to shiga toxin; factor h deficiency; and aberrant von willebrand factor formation.

What is a microangiopathic hemolytic anemia?

A disorder characterized by the presence of microangiopathic hemolytic anemia, thrombocytopenic purpura, fever, renal abnormalities and neurological abnormalities such as seizures, hemiplegia, and visual disturbances. It is an acute or subacute condition.