Home > 2013 ICD-9-CM Diagnosis Codes > Diseases Of The Blood And Blood-Forming Organs 280-289 > Coagulation defects 286-
2013 ICD-9-CM Diagnosis Code 286.9
Other and unspecified coagulation defects
- condition in which there is a deviation from or interruption of the normal coagulation properties of the blood.
- A condition in which there is a deviation from or interruption of the normal coagulation properties of the blood.
- ICD-9-CM 286.9 is a billable medical code that can be used to specify a diagnosis on a reimbursement claim.
286.9 Alternative Terminology
- 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 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
286.9 Excludes 
Applies To
- Defective coagulation NOS
- Deficiency, coagulation factor NOS
- Delay, coagulation
- Disorder:
- coagulation
- hemostasis
Convert 286.9 to ICD-10-CM
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
- consumption 286.6
- Defect, defective 759.9
- clotting NEC (see also Defect, coagulation) 286.9
- coagulation (factor) (see also Deficiency, coagulation factor) 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
- combined, two or more coagulation factors (see also Defect, coagulation) 286.9
- factor (see also Defect, coagulation) 286.9
I (congenital) (fibrinogen) 286.3- 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
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, coagulation (see also Defect, coagulation) 286.9
- 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 2013 ICD-9-CM Index or use the search engine at the top of this page to lookup any code.
|
Free 2013 ICD-9-CM Codes
|
Free 2013 ICD-10-CM/PCS Codes
|
|
Free 2007-2012 ICD-9-CM Codes
|
Free 2007-2013 HCPCS Codes
|
|
Site Information
|