ICDcodes.org
FY2027

D68.022Von Willebrand disease, type 2M

BillableCC

Is D68.022 billable?

Yes — D68.022 is billable for FY2027. D68.022 is a valid, billable ICD-10-CM code at the highest level of specificity in its branch. D68.022 may be submitted for encounters from October 1, 2026 through September 30, 2027.

D68.022 at a glance

CodeD68.022
DescriptionVon Willebrand disease, type 2M
BillableYes
Code setICD-10-CM FY2027
Valid for encountersOctober 1, 2026 – September 30, 2027

Which MS-DRGs does D68.022 group to?

D68.022 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, D68.022 is a complication or comorbidity (CC), which can move a stay into a higher-paying DRG.

How is D68.022 listed in the Alphabetic Index?

These are the routes through the Alphabetic Index that lead to D68.022. They show the wording a clinician may have documented, which often differs from the Tabular description.

  • Defect, defectivequalitative, of von Willebrand factorwithdefective platelet adhesion with a normal size distribution of von Willebrand factor multimers
  • Disease, diseasedvon Willebrandtype 2type 2M

Inclusion terms

Alternative wording in documentation that is classified to D68.022.

  • Qualitative defects of von Willebrand factor with defective platelet adhesion with a normal size distribution of von Willebrand factor multimers

Excludes1 — never code together — inherited from D68

The conditions below can never be reported together with D68.022 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 D68.022 on the same claim. An Excludes1 note means the two conditions cannot occur in the same patient, so reporting both is a coding error.

  • capillary fragility (hereditary) (D69.8)
  • factor VIII deficiency NOS (D66)
  • factor VIII deficiency with functional defect (D66)

Excludes2 — not included here — inherited from Chapter 3

The conditions below are not part of D68.022, but a patient may have both at the same time. When documentation supports it, D68.022 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 D68.022, but a patient may have both at the same time. When documentation supports it, D68.022 and the excluded code may both be reported.

  • coagulation defects complicating abortion or ectopic or molar pregnancy (O00-O07, O08.1)
  • coagulation defects complicating pregnancy, childbirth and the puerperium (O45.0, O46.0, O67.0, O72.3)

How long has D68.022 existed?

D68.022 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.

What other codes are in the D68.02 family? (4)