2014 ICD-9-CM Diagnosis Code 286.0
Congenital factor VIII disorder
- Short description: Cong factor viii diord.
- ICD-9-CM 286.0 will be replaced by an equivalent ICD-10-CM code (or codes) when the United States transitions from ICD-9-CM to ICD-10-CM on October 1, 2015.
- ICD-9-CM 286.0 is a billable medical code that can be used to specify a diagnosis on a reimbursement claim.
- Hemophilia A
- Hemophilic arthropathy
- Hereditary factor VIII deficiency disease
- A deficiency or abnormality of a blood coagulation factor characterized by the tendency to spontaneous or exaggerated post-traumatic hemorrhage, hemophilia is typically a hereditary disorder but, rarely, may be acquired. Inherited coagulation factor-deficient hemophilias include hemophilia a or classic hemophilia (factor viii deficiency) hemophilia b or christmas disease (factor ix deficiency), and hemophilia c (factor xi deficiency). In individuals without hereditary hemophilia a, factor viii inhibitors may occur spontaneously as autoantibodies, resulting in a condition known as 'acquired hemophilia.' approximately 10 % of patients with acquired hemophilia have an underlying malignancy.
- An inherited deficiency of coagulation factor viii characterized by the tendency to spontaneous or exaggerated post-traumatic hemorrhage. Inherited as an x-linked recessive disease, hemophilia a is the most common hemophilia, occurring in approximately 1 in 10,000 male births.
- Classic hemophilia resulting from a deficiency of factor viii; an inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhage.
- Group of hereditary disorders in which affected individuals fail to make enough of certain proteins needed to form blood clots.
- factor VIII deficiency with vascular defect (286.4)
- Antihemophilic globulin [AHG] deficiency
- Factor VIII (functional) deficiency
Convert to ICD-10-CM
converts directly to:
- 2014 ICD-10-CM D66 Hereditary factor VIII deficiency