2006 ICD-9-CM Diagnosis Code 286.9
Other and unspecified coagulation defects
- Short description: COAGULAT DEFECT NEC/NOS.
- ICD-9-CM 286.9 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 286.9 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 2006 version of ICD-9-CM 286.9.
- More recent version(s) of ICD-9-CM 286.9: 2007 2008 2009 2010 2011 2012 2013 2014 2015.
Convert to ICD-10-CM:
286.9 converts approximately to:
- 2015/16 ICD-10-CM D68.8 Other specified coagulation defects
Or:
- 2015/16 ICD-10-CM D68.9 Coagulation defect, unspecified
Approximate 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
Applies To
- Defective coagulation NOS
- Deficiency, coagulation factor NOS
- Delay, coagulation
- Disorder:
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
- due to
- newborn, transient 776.3
- postpartum 666.3
- specified type NEC 286.3
- 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
- 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
- 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
