D68.2 – Hereditary deficiency of other clotting factors
ICD-10-CM 2027 diagnosis code · Coagulation defects, purpura and other hemorrhagic conditions
- Code
D68.2(claims format:D682)- Description
- Hereditary deficiency of other clotting factors
- Billable
- Yes – valid for HIPAA-covered transactions
- Valid for
- Dates of service October 1, 2026 – September 30, 2027 (FY2027)
- Chapter
- 3. Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89)
- Block
- D65-D69 Coagulation defects, purpura and other hemorrhagic conditions
- Parent codes
- D68
Notes for D68.2
- AC globulin deficiency
- Congenital afibrinogenemia
- Deficiency of factor I [fibrinogen]
- Deficiency of factor II [prothrombin]
- Deficiency of factor V [labile]
- Deficiency of factor VII [stable]
- Deficiency of factor X [Stuart-Prower]
- Deficiency of factor XII [Hageman]
- Deficiency of factor XIII [fibrin stabilizing]
- Dysfibrinogenemia (congenital)
- Hypoproconvertinemia
- Owren's disease
- Proaccelerin deficiency
Notes inherited from parent codes
Instructional notes at a category or block level apply to every code below it.
D68 – Other coagulation defects
- abnormal coagulation profile NOS (R79.1)
Index terms for D68.2
Entries in the ICD-10-CM alphabetic index that lead to this code:
- Fibrinopenia
- Parahemophilia
- Syndrome, Owren's
- Dysfibrinogenemia
- Absence, fibrinogen
- Hypoprothrombinemia
- Stuart deficiency disease
- Defect, defective, Hageman
- Disease, diseased, Hageman
- Afibrinogenemia, congenital
- Owren's disease or syndrome
- Disease, diseased, Stuart's
- Deficiency, deficient, SPCA
- Fibrinogenopenia, congenital
- Hypofibrinogenemia, congenital
- Stuart-Prower factor deficiency
- Deficiency, deficient, factor, I
- Disease, diseased, Stuart-Prower
- Hypoproconvertinemia, congenital
- Deficiency, deficient, fibrinase
- Deficiency, deficient, factor, X
- Deficiency, deficient, factor, V
- Deficiency, deficient, fibrinogen
- Deficiency, deficient, factor, II
- Deficiency, deficient, factor, XII
Related codes in D68
- D68.0 – Von Willebrand diseaseHeader
- D68.1 – Hereditary factor XI deficiencyBillable
- D68.3 – Hemorrhagic disorder due to circulating anticoagulantsHeader
- D68.4 – Acquired coagulation factor deficiencyBillable
- D68.5 – Primary thrombophiliaHeader
- D68.6 – Other thrombophiliaHeader
- D68.8 – Other specified coagulation defectsBillable
- D68.9 – Coagulation defect, unspecifiedBillable
Frequently asked questions
What is ICD-10 code D68.2?
D68.2 is the ICD-10-CM code for hereditary deficiency of other clotting factors, in the block D65-D69 (Coagulation defects, purpura and other hemorrhagic conditions).
Is D68.2 a billable code?
Yes. D68.2 is a billable/specific code that can be used to indicate a diagnosis for reimbursement purposes.
What category does D68.2 belong to?
It belongs to category D68 – Other coagulation defects.
Source: CDC/NCHS ICD-10-CM FY2027 code files, tabular list and index. Reference only – code assignment must follow the official ICD-10-CM guidelines and documentation in the medical record.