D68.0 — Von Willebrand disease
Is D68.0 billable?
No — D68.0 is a non-billable header code. D68.0 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 10 billable codes beneath D68.0.
Billable codes under this header
- 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
- D68.020Von 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
D68.0 at a glance
| Code | D68.0 |
|---|---|
| Description | Von Willebrand disease |
| 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 D68.0 on the same claim. An Excludes1 note means the two conditions cannot occur in the same patient, so reporting both is a coding error.
Excludes1 — never code together — inherited from D68
The conditions below can never be reported together with D68.0 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 — inherited from Chapter 3
The conditions below are not part of D68.0, but a patient may have both at the same time. When documentation supports it, D68.0 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)
Excludes2 — not included here — inherited from D68
The conditions below are not part of D68.0, but a patient may have both at the same time. When documentation supports it, D68.0 and the excluded code may both be reported.
What codes fall under D68.0? (6)
How long has D68.0 existed?
D68.0 has been in ICD-10-CM since at least FY2016, the earliest fiscal year on record here.
- FY2023: D68.0 stopped being billable
- FY2023Von Willebrand's diseaseVon Willebrand disease
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 D68.0?
ICD-10-CM declares these codes mutually exclusive with D68.0 — exactly one of each pair can be correct for a given encounter.
What other codes are in the D68 family? (8)
- 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