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 286.3
Congenital deficiency of other clotting factors
- deficiency or absence of fibrinogen (coagulation factor I) in the blood.
- absence or reduced levels of prothrombin in the blood.
- ICD-9-CM 286.3 is a billable medical code that can be used to specify a diagnosis on a reimbursement claim.
286.3 Alternative Terminology
- Alpha chain defect dysfibrinogenemia
- Beta chain defect dysfibrinogenemia
- Congenital afibrinogenemia
- Congenital fibrinogen abnormality
- Congenital hypofibrinogenemia
- Contact factor deficiency
- Dysfibrinogenemia
- Factor i deficiency
- Factor i deficiency disease
- Factor ii deficiency
- Factor v deficiency
- Factor vii deficiency
- Factor x deficiency
- Factor xii deficiency disease
- Factor xiii deficiency disease
- Factor xiii inhibitor disorder
- Fibrinogen abnormality
- Fibrinogen deficiency
- Gamma chain defect dysfibrinogenemia
- Hemorrhagic disease of the newborn due to factor ii deficiency
- Heparin cofactor ii deficiency
- Hereditary dysfibrinogenemia
- Hereditary factor i deficiency disease
- Hereditary factor ii deficiency disease
- Hereditary factor v deficiency disease
- Hereditary factor vii deficiency disease
- Hereditary factor x deficiency disease
- Hereditary factor xii deficiency disease
- Hereditary factor xiii a subunit and b subunit deficiency
- Hereditary factor xiii a subunit deficiency
- Hereditary factor xiii deficiency disease
- Hyperfibrinogenemia
- Hypodysfibrinogenemia
- Hypofibrinogenemia
- Passovoy factor deficiency
- Platelet factor v deficiency
- Prothrombin complex deficiency
Applies To
- Congenital afibrinogenemia
- Deficiency:
- AC globulin
- factor:
- I [fibrinogen]
- II [prothrombin]
- V [labile]
- VII [stable]
- X [Stuart-Prower]
- XII [Hageman]
- XIII [fibrin stabilizing]
- Laki-Lorand factor
- proaccelerin
- Disease:
- Owren's
- Stuart-Prower
- Dysfibrinogenemia (congenital)
- Dysprothrombinemia (constitutional)
- Hypoproconvertinemia
- Hypoprothrombinemia (hereditary)
- Parahemophilia
Convert 286.3 to ICD-10-CM 
ICD-9-CM 286.3 converts directly to:
- 2013 ICD-10-CM D68.2 Hereditary deficiency of other clotting factors
ICD-9-CM Volume 2 Index entries containing back-references to 286.3:
- Absence (organ or part) (complete or partial)
fibrinogen (congenital) 286.3
acquired 286.6
- Afibrinogenemia 286.3
acquired 286.6
- congenital 286.3
- postpartum 666.3
- Defect, defective 759.9
- fibrin polymerization (see also Defect, coagulation) 286.3
- Hageman (factor) (see also Defect, coagulation) 286.3
- Deficiency, deficient
- accelerator globulin (Ac G) (blood) (see also Defect, coagulation) 286.3
- AC globulin (congenital) (see also Defect, coagulation) 286.3
acquired 286.7
- activating factor (blood) (see also Defect, coagulation) 286.3
- autoprothrombin
- I (see also Defect, coagulation) 286.3
- II 286.1
- C (see also Defect, coagulation) 286.3
- coagulation factor NEC 286.9
- contact factor (see also Defect, coagulation) 286.3
- 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
- fibrinase (see also Defect, coagulation) 286.3
- fibrinogen (congenital) (see also Defect, coagulation) 286.3
- acquired 286.6
- fibrin-stabilizing factor (congenital) (see also Defect, coagulation) 286.3
- acquired 286.7
- glass factor (see also Defect, coagulation) 286.3
- Hageman factor (congenital) (see also Defect, coagulation) 286.3
- labile factor (congenital) (see also Defect, coagulation) 286.3
- acquired 286.7
- laki-Lorand factor (see also Defect, coagulation) 286.3
- proaccelerin (congenital) (see also Defect, congenital) 286.3
- acquired 286.7
- proconvertin factor (congenital) (see also Defect, coagulation) 286.3
- acquired 286.7
- prothrombin (congenital) (see also Defect, coagulation) 286.3
- acquired 286.7
- Prower factor (see also Defect, coagulation) 286.3
- SPCA (see also Defect, coagulation) 286.3
- stable factor (congenital) (see also Defect, coagulation) 286.3
- acquired 286.7
- Stuart (-Prower) factor (see also Defect, coagulation) 286.3
- thrombokinase (see also Defect, coagulation) 286.3
- newborn 776.0
- Disease, diseased - see also Syndrome
- Hageman (congenital factor XII deficiency) (see also Defect, congenital) 286.3
- Owren's (congenital) (see also Defect, coagulation) 286.3
- Stuart's (congenital factor X deficiency) (see also Defect, coagulation) 286.3
- Stuart-Prower (congenital factor X deficiency) (see also Defect, coagulation) 286.3
- Dysfibrinogenemia (congenital) (see also Defect, coagulation) 286.3
- Dysprothrombinemia (constitutional) (see also Defect, coagulation) 286.3
- Fibrinogenopenia (congenital) (hereditary) (see also Defect, coagulation) 286.3
- acquired 286.6
- Fibrinopenia (hereditary) (see also Defect, coagulation) 286.3
- acquired 286.6
- Hageman factor defect, deficiency, or disease (see also Defect, coagulation) 286.3
- Hypofibrinogenemia 286.3
- acquired 286.6
- congenital 286.3
- Hypoproaccelerinemia (see also Defect, coagulation) 286.3
- Hypoproconvertinemia (congenital) (see also Defect, coagulation) 286.3
- Hypoprothrombinemia (congenital) (hereditary) (idiopathic) (see also Defect, coagulation) 286.3
- acquired 286.7
- newborn 776.3
- Laki-Lorand factor deficiency (see also Defect, coagulation) 286.3
- Owren's disease or syndrome (parahemophilia) (see also Defect, coagulation) 286.3
- Parahemophilia (see also Defect, coagulation) 286.3
- Stuart's disease (congenital factor X deficiency) (see also Defect, coagulation) 286.3
- Stuart-Prower factor deficiency (congenital factor X deficiency) (see also Defect, coagulation) 286.3
- Syndrome - see also Disease
- Owren's (see also Defect, coagulation) 286.3
ICD-9-CM codes are used in medical billing and coding to describe diseases, injuries, symptoms and conditions. ICD-9-CM 286.3 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.
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