Diagnosis Code: 286.9

Short Description: Coagulat defect NEC/NOS

Long Description: Other and unspecified coagulation defects

Code Classification:

• Diseases of the blood and blood-forming organs (280–289)
  • Diseases of the blood and blood-forming organs (280-289)
    • 286 Coagulation defects
      • 286.9 Coagulat defect NEC/NOS

Code Version: 2015 ICD-9-CM

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 complicating childbirth
• Blood coagulation disorder complicating 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 factor deficiency syndrome
• 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
• Prekallikrein deficiency
• Premature separation of placenta with coagulation defect
• Primary cryofibrinogenemia
• Pseudo von Willebrand disease
• Reactive thrombocytosis
• Systemic lupus erythematosus-associated antiphospholipid syndrome
• Thrombophilia

References to Index of Diseases and Injuries

The code 286.9 has the following ICD-9-CM references to the Index of Diseases and Injuries

• 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
  • consumption 286.6
  • intravascular (disseminated) NEC 286.6
    • newborn 776.2

• 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
      • liver disease 286.7
      • vitamin K deficiency 286.7
    • 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
      • liver disease 286.7
      • vitamin K deficiency 286.7
    • 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
      • 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
      • acquired 286.7
  • 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

• Hemorrhage, hemorrhagic (nontraumatic) 459.0
  • pregnancy (concealed) 641.9
    • due to
      • afibrinogenemia or other coagulation defect (conditions classifiable to 286.0-286.9) 641.3
        • affecting fetus or newborn 762.1

• Hypocoagulability (see also Defect, coagulation) 286.9

• Pregnancy (single) (uterine) (without sickness) V22.2
  • complicated (by) 646.9
    • hemorrhage 641.9
      • due to
        • afibrinogenemia or other coagulation defect (conditions classifiable to 286.0-286.9) 641.3

• Tendency
  • bleeding (see also Defect, coagulation) 286.9

Crosswalk Information

The code 286.9 converts into the following ICD-10 code(s):

Similar Codes

This page was last updated on: 10/1/2014

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