2013 ICD-9-CM Diagnosis Code 286.0
Congenital factor VIII disorder
- classic hemophilia resulting from a deficiency of factor VIII; an inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhage.
- 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. --2004
- Group of hereditary disorders in which affected individuals fail to make enough of certain proteins needed to form blood clots.
- 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. --2004
- ICD-9-CM 286.0 is a billable medical code that can be used to specify a diagnosis on a reimbursement claim.
286.0 Alternative Terminology
286.0 Excludes 
)Applies To
Convert 286.0 to ICD-10-CM
ICD-9-CM Volume 2 Index entries containing back-references to 286.0:
antihemophilic
C 
