Home > 2013 ICD-9-CM Diagnosis Codes > Diseases Of The Blood And Blood-Forming Organs 280-289 > Coagulation defects 286-
Specific code 2013 ICD-9-CM Diagnosis Code 286.4
Von Willebrand's disease
  • ICD-9-CM 286.4 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 286.4 should only be used for claims with a date of service on or before September 30, 2015. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes).
  • You are viewing the 2013 version of ICD-9-CM 286.4.
  • More recent version(s) of ICD-9-CM 286.4: 2014 2015.
Convert to ICD-10-CM: 286.4 converts directly to:
  • 2015/16 ICD-10-CM D68.0 Von Willebrand's disease
Approximate Synonyms
  • Von willebrand disease
  • von Willebrand disorder
286.4 Excludes
  • factor VIII deficiency:
  • hereditary capillary fragility (287.8)
Applies To
  • Angiohemophilia (A) (B)
  • Constitutional thrombopathy
  • Factor VIII deficiency with vascular defect
  • Pseudohemophilia type B
  • Vascular hemophilia
  • von Willebrand's (-Jürgens') disease
ICD-9-CM Volume 2 Index entries containing back-references to 286.4:
  • Angiohemophilia (A) (B) 286.4
  • Defect, defective 759.9
    • platelet (qualitative) 287.1
      • constitutional 286.4
  • Deficiency, deficient
    • factor (see also Defect, coagulation) 286.9
      • I (congenital) (fibrinogen) 286.3
        • antepartum or intrapartum 641.3
          • affecting fetus or newborn 762.1
        • newborn, transient 776.3
        • postpartum 666.3
      • II (congenital) (prothrombin) 286.3
      • V (congenital) (labile) 286.3
      • VII (congenital) (stable) 286.3
      • VIII (congenital) (functional) 286.0
        • with
          • functional defect 286.0
          • vascular defect 286.4
      • IX (Christmas) (congenital) (functional) 286.1
      • X (congenital) (Stuart-Prower) 286.3
      • XI (congenital) (plasma thromboplastin antecedent) 286.2
      • XII (congenital) (Hageman) 286.3
      • XIII (congenital) (fibrin stabilizing) 286.3
      • hageman 286.3
      • multiple (congenital) 286.9
    • platelet NEC 287.1
      • constitutional 286.4
  • Disease, diseased - see also Syndrome
    • Minot-von Willebrand-Jürgens (angiohemophilia) 286.4
    • von Willebrand (-Jürgens) (angiohemophilia) 286.4
  • Hemophilia (familial) (hereditary) 286.0
    • vascular 286.4
  • Minot-von Willebrand (-Jürgens) disease or syndrome (angiohemophilia) 286.4
  • Prolonged, prolongation
    • "idiopathic" (in von Willebrand's disease) 286.4
  • Pseudohemophilia (Bernuth's) (hereditary) (type B) 286.4
  • Syndrome - see also Disease
    • von Willebrand (-Jürgens) (angiohemophilia) 286.4
    • Willebrand (-Jürgens) (angiohemophilia) 286.4
  • Thrombopathy (Bernard-Soulier) 287.1
    • constitutional 286.4
    • Willebrand-Jürgens (angiohemophilia) 286.4
  • von Willebrand (-Jürgens) (-Minot) disease or syndrome (angiohemophilia) 286.4
  • Willebrand (-Jürgens) syndrome or thrombopathy (angiohemophilia) 286.4
 286.3 ICD9Data.com 286.5 
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