D68.00

Von Willebrand disease, unspecified

Billable / specificHCC V28 112

D68.00 is a billable, specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes in FY2027.

Excludes1

Not coded here — never report together with this code.

  • capillary fragility (hereditary) (D69.8) (from D68.0)
  • factor VIII deficiency NOS (D66) (from D68.0)
  • factor VIII deficiency with functional defect (D66) (from D68.0)
  • abnormal coagulation profile NOS (R79.1) (from D68)

Excludes2

Not included here — may be reported together when both conditions exist.

  • autoimmune disease (systemic) NOS (M35.9) (from D68)
  • certain conditions originating in the perinatal period (P00-P96) (from D68)
  • complications of pregnancy, childbirth and the puerperium (O00-O9A) (from D68)
  • congenital malformations, deformations and chromosomal abnormalities (Q00-Q99) (from D68)
  • endocrine, nutritional and metabolic diseases (E00-E88) (from D68)
  • human immunodeficiency virus [HIV] disease (B20) (from D68)
  • injury, poisoning and certain other consequences of external causes (S00-T88) (from D68)
  • neoplasms (C00-D49) (from D68)
  • symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94) (from D68)
  • coagulation defects complicating abortion or ectopic or molar pregnancy (O00-O07, O08.1) (from D68)
  • coagulation defects complicating pregnancy, childbirth and the puerperium (O45.0, O46.0, O67.0, O72.3) (from D68)

Also known as

  • Disease, diseased, von Willebrand

Parent code

  • D68.0Von Willebrand diseaseHeader

Related codes

  • D68.01Von Willebrand disease, type 1Billable
  • D68.02Von Willebrand disease, type 2Header
  • D68.03Von Willebrand disease, type 3Billable
  • D68.04Acquired von Willebrand diseaseBillable
  • D68.09Other von Willebrand diseaseBillable

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