
2015 ICD-9-CM Diagnosis Code 286.0
Congenital factor VIII disorder
- 2015
- Billable Thru Sept 30/2015
- Non-Billable On/After Oct 1/2015
- ICD-9-CM 286.0 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 286.0 should only be used for claims with a date of service on or before September 30, 2015. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes).
Convert to ICD-10-CM:
286.0 converts directly to:
- 2015/16 ICD-10-CM D66 Hereditary factor VIII deficiency
Approximate Synonyms
- Hemophilia
- Hemophilia A
- Hemophilic arthritis
- Hemophilic arthropathy
- Hereditary factor VIII deficiency disease
Clinical Information
- 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
286.0 Excludes

- factor VIII deficiency with vascular defect (286.4
)
Applies To
- Antihemophilic globulin [AHG] deficiency
- Factor VIII (functional) deficiency
- Hemophilia:
- NOS
- A
- classical
- familial
- hereditary
- Subhemophilia