D68 — Other coagulation defects
Is D68 billable?
No — D68 is a non-billable header code. D68 groups more specific codes and cannot be submitted on a claim. A valid ICD-10-CM code must be reported at the highest level of specificity available in its branch. Select one of the 25 billable codes beneath D68.
Billable codes under this header
- D68.1Hereditary factor XI deficiency
- D68.2Hereditary deficiency of other clotting factors
- D68.4Acquired coagulation factor deficiency
- D68.8Other specified coagulation defects
- D68.9Coagulation defect, unspecified
- D68.00Von Willebrand disease, unspecified
- D68.01Von Willebrand disease, type 1
- D68.03Von Willebrand disease, type 3
- D68.04Acquired von Willebrand disease
- D68.09Other von Willebrand disease
- D68.32Hemorrhagic disorder due to extrinsic circulating anticoagulants
- D68.51Activated protein C resistance
- D68.52Prothrombin gene mutation
- D68.59Other primary thrombophilia
- D68.61Antiphospholipid syndrome
- D68.62Lupus anticoagulant syndrome
- D68.69Other thrombophilia
- D68.020Von Willebrand disease, type 2A
- D68.021Von Willebrand disease, type 2B
- D68.022Von Willebrand disease, type 2M
- D68.023Von Willebrand disease, type 2N
- D68.029Von Willebrand disease, type 2, unspecified
- D68.311Acquired hemophilia
- D68.312Antiphospholipid antibody with hemorrhagic disorder
- D68.318Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors
D68 at a glance
| Code | D68 |
|---|---|
| Description | Other coagulation defects |
| Billable | No — header code |
| Code set | ICD-10-CM FY2027 |
| Valid for encounters | October 1, 2026 – September 30, 2027 |
Excludes1 — never code together
The conditions below can never be reported together with D68 on the same claim. An Excludes1 note means the two conditions cannot occur in the same patient, so reporting both is a coding error.
- abnormal coagulation profile NOS (R79.1)
Excludes2 — not included here
The conditions below are not part of D68, but a patient may have both at the same time. When documentation supports it, D68 and the excluded code may both be reported.
Excludes2 — not included here — inherited from Chapter 3
The conditions below are not part of D68, but a patient may have both at the same time. When documentation supports it, D68 and the excluded code may both be reported.
- autoimmune disease (systemic) NOS (M35.9)
- certain conditions originating in the perinatal period (P00-P96)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- human immunodeficiency virus [HIV] disease (B20)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
What codes fall under D68? (9)
- D68.0Von Willebrand diseasenot billable
- D68.1Hereditary factor XI deficiency
- D68.2Hereditary deficiency of other clotting factors
- D68.3Hemorrhagic disorder due to circulating anticoagulantsnot billable
- D68.4Acquired coagulation factor deficiency
- D68.5Primary thrombophilianot billable
- D68.6Other thrombophilianot billable
- D68.8Other specified coagulation defects
- D68.9Coagulation defect, unspecified
How long has D68 existed?
D68 has been in ICD-10-CM since at least FY2016, the earliest fiscal year on record here.
Derived from the official order files for FY2016–FY2026. FY2017 and FY2020 publish no order file, so those years are not covered.
Which codes are confused with D68?
ICD-10-CM declares these codes mutually exclusive with D68 — exactly one of each pair can be correct for a given encounter.