D68.020 — Von Willebrand disease, type 2A
Is D68.020 billable?
Yes — D68.020 is billable for FY2027. D68.020 is a valid, billable ICD-10-CM code at the highest level of specificity in its branch. D68.020 may be submitted for encounters from October 1, 2026 through September 30, 2027.
D68.020 at a glance
| Code | D68.020 |
|---|---|
| Description | Von Willebrand disease, type 2A |
| Billable | Yes |
| Code set | ICD-10-CM FY2027 |
| Valid for encounters | October 1, 2026 – September 30, 2027 |
Which MS-DRGs does D68.020 group to?
D68.020 sits in MDC 16 and helps define the logic of 1 MS-DRG (version 44, FY2027). Which one a stay actually groups to also depends on procedures and secondary diagnoses.
- 813Coagulation Disordersmedical
As a secondary diagnosis, D68.020 is a complication or comorbidity (CC), which can move a stay into a higher-paying DRG.
How is D68.020 listed in the Alphabetic Index?
These are the routes through the Alphabetic Index that lead to D68.020. They show the wording a clinician may have documented, which often differs from the Tabular description.
- Defect, defective › qualitative, of von Willebrand factor › with › decreased platelet adhesion and selective deficiency of high-molecular-weight multimers
- Disease, diseased › von Willebrand › type 2 › type 2A
Inclusion terms
Alternative wording in documentation that is classified to D68.020.
- Qualitative defects of von Willebrand factor with decreased platelet adhesion and selective deficiency of high-molecular-weight multimers
Excludes1 — never code together — inherited from D68
The conditions below can never be reported together with D68.020 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)
Excludes1 — never code together — inherited from D68.0
The conditions below can never be reported together with D68.020 on the same claim. An Excludes1 note means the two conditions cannot occur in the same patient, so reporting both is a coding error.
Excludes2 — not included here — inherited from Chapter 3
The conditions below are not part of D68.020, but a patient may have both at the same time. When documentation supports it, D68.020 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 D68.020, but a patient may have both at the same time. When documentation supports it, D68.020 and the excluded code may both be reported.
How long has D68.020 existed?
D68.020 first appears in FY2023.
Derived from the official order files for FY2016–FY2026. FY2017 and FY2020 publish no order file, so those years are not covered.