2015 ICD-9-CM Diagnosis Code 286.3
Congenital deficiency of other clotting factors
- 2015
- Billable Thru Sept 30/2015
- Non-Billable On/After Oct 1/2015
- ICD-9-CM 286.3 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 286.3 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).
Convert to ICD-10-CM:
286.3 converts directly to:
- 2015/16 ICD-10-CM D68.2 Hereditary deficiency of other clotting factors
Approximate Synonyms
- Alpha chain defect dysfibrinogenemia
- Beta chain defect dysfibrinogenemia
- Clotting factor deficiency, congenital
- Congenital afibrinogenemia
- Congenital clotting factor deficiency
- Congenital coagulation factor deficiency
- Congenital dysfibrinogenemia
- Congenital fibrinogen abnormality
- Congenital hypofibrinogenemia
- Contact factor deficiency
- Dysfibrinogenemia
- Dysfibrinogenemia, congenital
- Factor 10 deficiency
- Factor 12 deficiency
- Factor 2 mutation
- Factor 5 deficiency
- Factor 7 deficiency
- Factor I deficiency
- Factor I deficiency disease
- Factor II deficiency
- Factor V deficiency
- Factor V deficiency, Quebec
- Factor V Quebec
- Factor VII deficiency
- Factor X deficiency
- Factor XII 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
- Placental abruption W afibrinogenemia
- Placental abruption with afibrinogenemia
- Platelet factor V deficiency
- Platelet factor V deficiency (factor V Quebec)
- Prothrombin complex deficiency
Clinical Information
- Absence or reduced levels of prothrombin in the blood
- Deficiency or absence of fibrinogen (coagulation factor i) in the blood
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:
- Dysfibrinogenemia (congenital)
- Dysprothrombinemia (constitutional)
- Hypoproconvertinemia
- Hypoprothrombinemia (hereditary)
- Parahemophilia
ICD-9-CM Volume 2 Index entries containing back-references to
286.3:
- Absence (organ or part) (complete or partial)
- fibrinogen (congenital) 286.3
- Afibrinogenemia 286.3
- congenital 286.3
- 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
- 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
- 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
- contact factor (see also Defect, coagulation) 286.3
- 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
- fibrinase (see also Defect, coagulation) 286.3
- fibrinogen (congenital) (see also Defect, coagulation) 286.3
- fibrin-stabilizing factor (congenital) (see also Defect, coagulation) 286.3
- 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
- laki-Lorand factor (see also Defect, coagulation) 286.3
- proaccelerin (congenital) (see also Defect, congenital) 286.3
- proconvertin factor (congenital) (see also Defect, coagulation) 286.3
- prothrombin (congenital) (see also Defect, coagulation) 286.3
- Prower factor (see also Defect, coagulation) 286.3
- SPCA (see also Defect, coagulation) 286.3
- stable factor (congenital) (see also Defect, coagulation) 286.3
- Stuart (-Prower) factor (see also Defect, coagulation) 286.3
- thrombokinase (see also Defect, coagulation) 286.3
- 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
- Fibrinopenia (hereditary) (see also Defect, coagulation) 286.3
- Hageman factor defect, deficiency, or disease (see also Defect, coagulation) 286.3
- Hypofibrinogenemia 286.3
- 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
- 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