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ALL MEDICAL CODES IN CATEGORY Coagulation defects, purpura and other hemorrhagic conditions

2025 ICD-10-CM code D68.0

Von Willebrand disease. This is a bleeding disorder characterized by a deficiency or dysfunction of von Willebrand factor (VWF), a protein crucial for blood clotting.

2025 ICD-10-CM code D69.4

Other primary thrombocytopenia. This code excludes transient neonatal thrombocytopenia (P61.0) and Wiskott-Aldrich syndrome (D82.0).

2025 ICD-10-CM code D68.00

Von Willebrand disease, unspecified.

2025 ICD-10-CM code D69.0

Allergic purpura is a condition causing inflammation of small blood vessels (capillaries) in the skin, kidneys, and intestines, often developing in children after an infection.

2025 ICD-10-CM code D65

Disseminated intravascular coagulation (DIC), also known as consumption coagulopathy or defibrination syndrome.

2025 ICD-10-CM code D69.49

Other primary thrombocytopenia. This condition involves a deficiency of platelets in the blood, not categorized elsewhere, leading to abnormal bleeding.

2025 ICD-10-CM code D68.59

Other primary thrombophilia. This is a blood disorder that increases the risk of blood clots.

2025 ICD-10-CM code D69.42

Congenital and hereditary thrombocytopenia purpura is an inherited disorder characterized by abnormal platelet function leading to excessive bleeding.

2025 ICD-10-CM code D69.2

Other nonthrombocytopenic purpura. This condition is characterized by bleeding under the skin causing red or purple spots, without a decrease in platelet count.

2025 ICD-10-CM code D68.029

Von Willebrand disease, type 2, unspecified. Qualitative defect in von Willebrand factor function, with no further subtyping.

2025 ICD-10-CM code D68.09

Other von Willebrand disease. This includes platelet-type and pseudo-von Willebrand disease.If applicable, also code qualitative platelet defects (D69.1).

2025 ICD-10-CM code D68.5

Primary thrombophilia. Increased tendency for blood clotting.

2025 ICD-10-CM code D68.318

Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors. This is a bleeding disorder caused by the body producing abnormal anticoagulants, antibodies against clotting factors, or coagulation inhibitors.

2025 ICD-10-CM code D68.51

Activated protein C resistance due to Factor V Leiden mutation.

2025 ICD-10-CM code D69.1

Qualitative platelet defects, including Bernard-Soulier syndrome, Glanzmann's disease, Grey platelet syndrome, Thromboasthenia, and Thrombocytopathy.

2025 ICD-10-CM code D68.69

This code represents a thrombophilia, a condition that increases the risk of blood clots, that is not otherwise specified.

2025 ICD-10-CM code D68.61

Antiphospholipid syndrome, also known as anticardiolipin syndrome or antiphospholipid antibody syndrome.

2025 ICD-10-CM code D68.312

Antiphospholipid antibody with hemorrhagic disorder.This condition involves bleeding due to the presence of antiphospholipid antibodies.

2025 ICD-10-CM code D68.04

Acquired von Willebrand disease, also known as Acquired von Willebrand syndrome.

2025 ICD-10-CM code D69.51

Posttransfusion purpura (PTP) is an adverse reaction to blood or platelet transfusion, causing sudden thrombocytopenia about 7-10 days post-transfusion.

2025 ICD-10-CM code D69.8

Other specified hemorrhagic conditions.Includes capillary fragility (hereditary) and vascular pseudohemophilia.

2025 ICD-10-CM code D69.41

Evans syndrome. This is a rare autoimmune disorder where the immune system attacks blood cells, leading to hemolytic anemia and thrombocytopenia.

2025 ICD-10-CM code D68.52

Prothrombin gene mutation, a disorder causing increased blood clotting risk.

2025 ICD-10-CM code D69.5

Secondary thrombocytopenia.A condition characterized by a low platelet count resulting from another underlying medical issue.

2025 ICD-10-CM code D69.6

A condition characterized by a low platelet count, essential for blood clotting.The cause is unspecified.