ICD-10-CM Code For Other Coagulation Defects: Group Overview

The International Classification of Diseases, Tenth Revision, Clinical Modification (ICD-10-CM) code group D68 includes a range of inherited and acquired coagulation disorders, such as deficiencies of clotting factors, anticoagulant abnormalities, and other hemorrhagic conditions that impair normal hemostasis. These ICD-10-CM diagnosis codes are used to document clinical presentations involving bleeding tendencies, thrombotic events, or coagulopathy secondary to other diseases, capturing disease severity, organ involvement, or clinical complexity relevant to this group. Accurate coding within the ICD-10-CM D68 group supports proper claim adjudication, complete clinical documentation, and appropriate reimbursement.

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ICD-10-CM D68: Other Coagulation Defects Overview

The other coagulation defects group includes inherited and acquired disorders of blood coagulation that lead to bleeding or thrombosis and other hemorrhagic conditions. These diagnoses primarily affect the hematologic system and hemostasis mechanisms. Accurate coding matters for appropriate clinical documentation and reimbursement because specificity influences claim adjudication and care tracking.

When to Use

Use codes from this group when a patient has documented abnormal coagulation function due to a specific factor deficiency, antibody-mediated coagulopathy, or other hemorrhagic condition. Select the most specific code that reflects the identified disorder, associated complications, and any underlying cause when documented in the medical record.

ICD-10-CM Codes

25 rows

ICD-10-CM Code	Description
D68.00	Von Willebrand disease, unspecified
D68.01	Von Willebrand disease, type 1
D68.020	Von Willebrand disease, type 2A
D68.021	Von Willebrand disease, type 2B
D68.022	Von Willebrand disease, type 2M
D68.023	Von Willebrand disease, type 2N
D68.029	Von Willebrand disease, type 2, unspecified
D68.03	Von Willebrand disease, type 3
D68.04	Acquired von Willebrand disease
D68.09	Other von Willebrand disease
D68.1	Hereditary factor XI deficiency
D68.2	Hereditary deficiency of other clotting factors
D68.311	Acquired hemophilia
D68.312	Antiphospholipid antibody with hemorrhagic disorder
D68.318	Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors
D68.32	Hemorrhagic disorder due to extrinsic circulating anticoagulants
D68.4	Acquired coagulation factor deficiency
D68.51	Activated protein C resistance
D68.52	Prothrombin gene mutation
D68.59	Other primary thrombophilia

Showing 1–20 of 25

DRG Codes

4 rows

DRG Code	Description
813	Coagulation Disorders
814	Reticuloendothelial and Immunity Disorders with MCC
815	Reticuloendothelial and Immunity Disorders with CC
816	Reticuloendothelial and Immunity Disorders without CC/MCC

Typical Clinical Scenarios

A middle-aged woman presents to the emergency department with sudden onset of large-volume hematuria and spontaneous skin ecchymoses after several days of antibiotic therapy; laboratory testing shows markedly prolonged bleeding times and a new severe thrombocytopenia consistent with immune-mediated platelet destruction. A diagnosis from this coagulation defects group is assigned because the presentation represents an acute hemorrhagic disorder requiring identification of the specific coagulation or platelet abnormality. Typical codes: D68.3, D68.32
A 45-year-old man with a long history of recurrent deep bruising and mucosal bleeding since childhood is seen in hematology for evaluation of a chronic bleeding diathesis; platelet function studies reveal an inherited platelet function disorder with abnormal aggregation but stable platelet counts. A code from this group is assigned to document the chronic platelet function defect as the cause of bleeding and for ongoing management and counseling. Typical codes: D68.4, D68.9
An elderly patient is admitted for hip fracture repair and develops postoperative diffuse oozing and prolonged coagulation studies while on therapeutic anticoagulation for atrial fibrillation; clinicians must identify the specific coagulation defect contributing to surgical bleeding to guide reversal and perioperative care. A diagnosis from this group is used to capture the acquired coagulation defect complicating the surgical course. Typical codes: D68.20, D68.29

ICD-10-CM Code For Disseminated Intravascular Coagulation Defibrination Syndrome: Group Overview

D66-HEREDITARY-FACTOR-VIII-DEFICIENCY

ICD-10-CM Code For Hereditary Factor VIII Deficiency: Group Overview

D67-HEREDITARY-FACTOR-IX-DEFICIENCY

ICD-10-CM Code For Hereditary Factor IX Deficiency: Group Overview

D69-PURPURA-AND-HEMORRHAGIC-CONDITIONS

ICD-10-CM Code For Purpura And Other Hemorrhagic Conditions: Group Overview

Frequently Asked Questions

References

1.CPT® Codes and Descriptions. AAPC. Retrieved Aug 11, 2026.Maintains the CPT code set's official descriptions and guidelines, licensed from the American Medical Association, used as the definitional source for CPT codes on this page.
2.HCPCS Quarterly Update. Centers for Medicare & Medicaid Services (CMS). Retrieved Aug 11, 2026.CMS's quarterly release of HCPCS Level II codes and short/long descriptors, the source for HCPCS code definitions and update history.
3.ICD-10-CM Full Code List. Centers for Medicare & Medicaid Services (CMS). Retrieved Aug 11, 2026.CMS's complete ICD-10-CM diagnosis code list, used to cross-reference diagnosis codes associated with this procedure or service.

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When to Use

ICD-10-CM Codes

25 rows

ICD-10-CM Code	Description
D68.00	Von Willebrand disease, unspecified
D68.01	Von Willebrand disease, type 1
D68.020	Von Willebrand disease, type 2A
D68.021	Von Willebrand disease, type 2B
D68.022	Von Willebrand disease, type 2M
D68.023	Von Willebrand disease, type 2N
D68.029	Von Willebrand disease, type 2, unspecified
D68.03	Von Willebrand disease, type 3
D68.04	Acquired von Willebrand disease
D68.09	Other von Willebrand disease
D68.1	Hereditary factor XI deficiency
D68.2	Hereditary deficiency of other clotting factors
D68.311	Acquired hemophilia
D68.312	Antiphospholipid antibody with hemorrhagic disorder
D68.318	Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors
D68.32	Hemorrhagic disorder due to extrinsic circulating anticoagulants
D68.4	Acquired coagulation factor deficiency
D68.51	Activated protein C resistance
D68.52	Prothrombin gene mutation
D68.59	Other primary thrombophilia

Showing 1–20 of 25

DRG Codes

4 rows

DRG Code	Description
813	Coagulation Disorders
814	Reticuloendothelial and Immunity Disorders with MCC
815	Reticuloendothelial and Immunity Disorders with CC
816	Reticuloendothelial and Immunity Disorders without CC/MCC

Typical Clinical Scenarios

A middle-aged woman presents to the emergency department with sudden onset of large-volume hematuria and spontaneous skin ecchymoses after several days of antibiotic therapy; laboratory testing shows markedly prolonged bleeding times and a new severe thrombocytopenia consistent with immune-mediated platelet destruction. A diagnosis from this coagulation defects group is assigned because the presentation represents an acute hemorrhagic disorder requiring identification of the specific coagulation or platelet abnormality. Typical codes: D68.3, D68.32
A 45-year-old man with a long history of recurrent deep bruising and mucosal bleeding since childhood is seen in hematology for evaluation of a chronic bleeding diathesis; platelet function studies reveal an inherited platelet function disorder with abnormal aggregation but stable platelet counts. A code from this group is assigned to document the chronic platelet function defect as the cause of bleeding and for ongoing management and counseling. Typical codes: D68.4, D68.9
An elderly patient is admitted for hip fracture repair and develops postoperative diffuse oozing and prolonged coagulation studies while on therapeutic anticoagulation for atrial fibrillation; clinicians must identify the specific coagulation defect contributing to surgical bleeding to guide reversal and perioperative care. A diagnosis from this group is used to capture the acquired coagulation defect complicating the surgical course. Typical codes: D68.20, D68.29

ICD-10-CM Code For Disseminated Intravascular Coagulation Defibrination Syndrome: Group Overview

D66-HEREDITARY-FACTOR-VIII-DEFICIENCY

ICD-10-CM Code For Hereditary Factor VIII Deficiency: Group Overview

D67-HEREDITARY-FACTOR-IX-DEFICIENCY

ICD-10-CM Code For Hereditary Factor IX Deficiency: Group Overview

D69-PURPURA-AND-HEMORRHAGIC-CONDITIONS

ICD-10-CM Code For Purpura And Other Hemorrhagic Conditions: Group Overview

Frequently Asked Questions

References

1.CPT® Codes and Descriptions. AAPC. Retrieved Aug 11, 2026.Maintains the CPT code set's official descriptions and guidelines, licensed from the American Medical Association, used as the definitional source for CPT codes on this page.
2.HCPCS Quarterly Update. Centers for Medicare & Medicaid Services (CMS). Retrieved Aug 11, 2026.CMS's quarterly release of HCPCS Level II codes and short/long descriptors, the source for HCPCS code definitions and update history.
3.ICD-10-CM Full Code List. Centers for Medicare & Medicaid Services (CMS). Retrieved Aug 11, 2026.CMS's complete ICD-10-CM diagnosis code list, used to cross-reference diagnosis codes associated with this procedure or service.

Published by

Trek Health powers OpenPayer with a leading commercial payer intelligence platform, seamlessly converting fragmented payer data into actionable insights for provider organizations.

ICD-10-CM Code For Other Coagulation Defects: Group Overview

Sign up for ICD-10-CM Code For Other Coagulation Defects: Group Overview policy alerts

ICD-10-CM D68: Other Coagulation Defects Overview

ICD-10-CM Code For Other Coagulation Defects: Group Overview

Sign up for ICD-10-CM Code For Other Coagulation Defects: Group Overview policy alerts

ICD-10-CM D68: Other Coagulation Defects Overview

When to Use

ICD-10-CM Codes

DRG Codes

Typical Clinical Scenarios

Related Codes

References

When to Use

ICD-10-CM Codes

DRG Codes

Typical Clinical Scenarios

Related Codes

References

ICD-10-CM Code For Other Coagulation Defects: Group Overview

Sign up for ICD-10-CM Code For Other Coagulation Defects: Group Overview policy alerts

ICD-10-CM D68: Other Coagulation Defects Overview

ICD-10-CM Code For Other Coagulation Defects: Group Overview

Sign up for ICD-10-CM Code For Other Coagulation Defects: Group Overview policy alerts

ICD-10-CM D68: Other Coagulation Defects Overview

When to Use

ICD-10-CM Codes

DRG Codes

Typical Clinical Scenarios

Related Codes

Which ICD-10-CM codes in group D68 represent von Willebrand disease subtypes?

Which D68 codes indicate acquired coagulation disorders rather than hereditary ones?

Which codes describe thrombophilia and related prothrombotic conditions in D68?

How does specificity within the D68 group affect billing and documentation?

Which DRGs are related to coagulation defects as listed in the content?

References

When to Use

ICD-10-CM Codes

DRG Codes

Typical Clinical Scenarios

Related Codes

Which ICD-10-CM codes in group D68 represent von Willebrand disease subtypes?

Which D68 codes indicate acquired coagulation disorders rather than hereditary ones?

Which codes describe thrombophilia and related prothrombotic conditions in D68?

How does specificity within the D68 group affect billing and documentation?

Which DRGs are related to coagulation defects as listed in the content?

References