D68.0 Von Willebrand disease

Non-billable header with 6 child codes.

Excludes1 (never code together)

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

Applies from D68 Other coagulation defects

Excludes1 (never code together)

• abnormal coagulation profile NOS (R79.1)

Excludes2 (not included here)

• 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)

Codes under D68.0

• D68.00 Von Willebrand disease, unspecified
• D68.01 Von Willebrand disease, type 1
• D68.02 Von Willebrand disease, type 2
• D68.03 Von Willebrand disease, type 3
• D68.04 Acquired von Willebrand disease
• D68.09 Other von Willebrand disease

Approximate ICD-9-CM (GEMs)

• 286.4 Von Willebrand's disease

Code annotations containing back-references to D68.0

Back-references to D68.0

• Type 1 Excludes: D66 Hereditary factor VIII deficiency ("factor VIII deficiency with vascular defect (D68.0-)")
• Type 2 Excludes: D69.1 Qualitative platelet defects ("von Willebrand disease (D68.0-)")
• Code First: M36.2 Hemophilic arthropathy ("with vascular defect (D68.0-)")
• Type 1 Excludes: R04.81 Acute idiopathic pulmonary hemorrhage in infants ("von Willebrand disease (D68.0-)")

Back-references to D68

• Type 1 Excludes: R79.1 Abnormal coagulation profile ("coagulation defects (D68.-)")

Nearby codes

• D68 Other coagulation defects
• D68.0 Von Willebrand disease (this code)
• D68.00 Von Willebrand disease, unspecified
• D68.01 Von Willebrand disease, type 1
• D68.02 Von Willebrand disease, type 2
• D68.020 Von Willebrand disease, type 2A
• D68.021 Von Willebrand disease, type 2B