D68.1

Applicable To

• Hemophilia C

• Plasma thromboplastin antecedent [PTA] deficiency

• Rosenthal’s disease

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.

Details

• D68.1 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.

• The 2023 edition of ICD-10-CM D68.1 became effective on October 1, 2022.

• This is the American ICD-10-CM version of D68.1 – other international versions of ICD-10 D68.1 may differ.