Specific code 2011 ICD-9-CM Diagnosis Code 286.9
Other and unspecified coagulation defects
  • Short description: Coagulat defect NEC/NOS.
  • ICD-9-CM 286.9 will be replaced by an equivalent ICD-10-CM code (or codes) when the United States transitions from ICD-9-CM to ICD-10-CM on October 1, 2015.
  • ICD-9-CM 286.9 is a billable medical code that can be used to specify a diagnosis on a reimbursement claim.
  • You are viewing the 2011 version of ICD-9-CM 286.9.
  • More recent version(s) of ICD-9-CM 286.9: 2012 2013 2014.
Disease Synonyms
  • Acquired coagulation disorder
  • Acquired coagulation factor deficiency
  • Acquired combined coagulation factor deficiency
  • Acquired factor X deficiency disease
  • Acquired fibrinogen abnormality
  • Acquired inhibitor of coagulation
  • Alpha-2-antiplasmin deficiency
  • Anticoagulant excess without bleeding
  • Anticoagulant-induced bleeding
  • Anti-factor II disorder
  • Antithrombin III deficiency
  • Bite of unidentified snake with coagulopathy
  • Bleeds easily
  • Bleeds profusely
  • Blood coagulation disorder
  • Blood coagulation disorder in childbirth
  • Blood coagulation disorder in pregnancy
  • Blood coagulation disorder with impaired clot retraction time
  • Blood coagulation disorder with prolonged bleeding time
  • Blood coagulation disorder with prolonged coagulation time
  • Blood coagulation disorder with shortened bleeding time
  • Blood coagulation disorder with shortened coagulation time
  • Blood does not clot properly
  • Coagulation condition in childbirth
  • Coagulation defect in childbirth
  • Coagulation defect in pregnancy
  • Coagulation factor deficiency syndrome
  • Coagulopathy
  • Coagulopathy (clotting or bleeding disorder)
  • Combined coagulation factor deficiency
  • Cryofibrinogenemia
  • Deficiency of naturally occurring coagulation factor inhibitor
  • Deficiency of thrombin
  • Dermite ocre of Favre
  • Factor V inhibitor disorder
  • Factor X inhibitor disorder
  • Familial multiple factor deficiency syndrome
  • Familial multiple factor deficiency syndrome, type I
  • Familial multiple factor deficiency syndrome, type II
  • Familial multiple factor deficiency syndrome, type III
  • Familial multiple factor deficiency syndrome, type IV
  • Familial multiple factor deficiency syndrome, type V
  • Familial multiple factor deficiency syndrome, type VI
  • Fibrinogen in blood above reference range
  • Hereditary coagulation factor deficiency
  • Hereditary combined coagulation factor deficiency
  • Hereditary elevated factor VIII
  • Hereditary elevated factor XI
  • Hereditary hyperfibrinogenemia
  • Hereditary thrombophilic dysfibrinogenemia
  • Heterozygous Factor V Leiden mutation
  • High molecular weight kininogen deficiency
  • Homozygous Factor V Leiden mutation
  • Ineffective thrombopoiesis
  • Placental abruption W coagulation defect
  • Placental abruption with coagulation defect
  • Prekallikrein deficiency
  • Premature separation of placenta with coagulation defect
  • Primary cryofibrinogenemia
  • Pseudo von Willebrand disease
  • Reactive thrombocytosis
  • Systemic lupus erythematosus-associated antiphospholipid syndrome
  • Thrombophilia
286.9 Excludes
  • abnormal coagulation profile (790.92)
  • hemorrhagic disease of newborn (776.0)
  • that complicating:
Applies To
  • Defective coagulation NOS
  • Deficiency, coagulation factor NOS
  • Delay, coagulation
  • Disorder:
    • coagulation
    • hemostasis
Convert to ICD-10-CM: 286.9 converts approximately to:
  • 2014 ICD-10-CM D68.8 Other specified coagulation defects
    Or:
  • 2014 ICD-10-CM D68.9 Coagulation defect, unspecified
ICD-9-CM Volume 2 Index entries containing back-references to 286.9:
  • Abnormal, abnormality, abnormalities - see also Anomaly
    • Dynia (see also Defect, coagulation) 286.9
  • Bleeder (familial) (hereditary) (see also Defect, coagulation) 286.9
    • nonfamilial 286.9
  • Bleeding (see also Hemorrhage) 459.0
    • familial (see also Defect, coagulation) 286.9
    • tendencies (see also Defect, coagulation) 286.9
  • Clotting defect NEC (see also Defect, coagulation) 286.9
  • Coagulopathy (see also Defect, coagulation) 286.9
    • intravascular (disseminated) NEC 286.6
  • Defect, defective 759.9
    • clotting NEC (see also Defect, coagulation) 286.9
    • coagulation (factor) (see also Deficiency, coagulation factor) 286.9
      • with
        • abortion - see Abortion, by type, with hemorrhage
        • ectopic pregnancy (see also categories 634-638) 639.1
        • molar pregnancy (see also categories 630-632) 639.1
      • acquired (any) 286.7
      • antepartum or intrapartum 641.3
        • affecting fetus or newborn 762.1
      • causing hemorrhage of pregnancy or delivery 641.3
      • complicating pregnancy, childbirth, or puerperium 649.3
      • due to
      • newborn, transient 776.3
      • postpartum 666.3
      • specified type NEC 286.9
  • Deficiency, deficient
    • Carr factor (see also Defect, coagulation) 286.9
    • clotting (blood) (see also Defect, coagulation) 286.9
    • coagulation factor NEC 286.9
      • with
        • abortion - see Abortion, by type, with hemorrhage
        • ectopic pregnancy (see also categories 634-638) 639.1
        • molar pregnancy (see also categories 630-632) 639.1
      • acquired (any) 286.7
      • antepartum or intrapartum 641.3
        • affecting fetus or newborn 762.1
      • complicating pregnancy, childbirth, or puerperium 649.3
      • due to
      • newborn, transient 776.3
      • postpartum 666.3
      • specified type NEC 286.3
    • combined, two or more coagulation factors (see also Defect, coagulation) 286.9
    • 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
      • 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
    • fletcher factor (see also Defect, coagulation) 286.9
  • Disease, diseased - see also Syndrome
    • coagulation factor deficiency (congenital) (see also Defect, coagulation) 286.9
  • Disorder - see also Disease
    • bleeding 286.9
    • coagulation (factor) (see also Defect, coagulation) 286.9
      • factor VIII (congenital) (functional) 286.0
      • factor IX (congenital) (functional) 286.1
      • neonatal, transitory 776.3
    • factor, coagulation (see also Defect, coagulation) 286.9
      • VIII (congenital) (functional) 286.0
      • IX (congenital) (functional) 286.1
    • hemostasis (see also Defect, coagulation) 286.9
  • Disturbance - see also Disease
    • blood clotting (hypoproteinemia) (mechanism) (see also Defect, coagulation) 286.9
  • Dynia abnormality (see also Defect, coagulation) 286.9
  • Hypocoagulability (see also Defect, coagulation) 286.9
  • Tendency
    • bleeding (see also Defect, coagulation) 286.9
ICD-9-CM codes are used in medical billing and coding to describe diseases, injuries, symptoms and conditions. ICD-9-CM 286.9 is one of thousands of ICD-9-CM codes used in healthcare. Although ICD-9-CM and CPT codes are largely numeric, they differ in that CPT codes describe medical procedures and services. Can't find a code? Start at the root of ICD-9-CM, check the 2011 ICD-9-CM Index or use the search engine at the top of this page to lookup any code.