2015 ICD-9-CM Diagnosis Code 286.2
Congenital factor XI deficiency
- 2015
- Billable Thru Sept 30/2015
- Non-Billable On/After Oct 1/2015
- ICD-9-CM 286.2 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 286.2 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:
286.2 converts directly to:
- 2015/16 ICD-10-CM D68.1 Hereditary factor XI deficiency
Approximate Synonyms
- Factor XI deficiency, type I
- Hemophilia C
- Hemophilia C, type 1
- Hereditary factor XI deficiency disease
Clinical Information
- A hereditary deficiency of blood coagulation factor xi (also known as plasma thromboplastin antecedent or pta or antihemophilic factor c) resulting in a systemic blood-clotting defect called hemophilia c or rosenthal's syndrome, that may resemble classical hemophilia
- A rare inherited bleeding disorder caused by deficiency of coagulation factor xi. It may be asymptomatic or manifest with bleeding
Applies To
- Hemophilia C
- Plasma thromboplastin antecedent [PTA] deficiency
- Rosenthal's disease
factor (see also Defect, coagulation) 286.9
multiple (congenital) 286.9
