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2007 ICD-9-CM Volume 1 Diagnosis Codes Home > Diseases Of Blood And Blood-Forming Organs 280-289 > Coagulation Defects 286.* > 2007 ICD-9-CM Diagnosis 286.3 Congenital deficiency of other clotting factors This code may be outdated. View the most recent version of ICD-9-CM 286.3 A deficiency of blood coagulation factor V (known as proaccelerin or accelerator globulin or labile factor) leading to a rare hemorrhagic tendency known as Owren's disease or parahemophilia. It varies greatly in severity. Factor V deficiency is an autosomal recessive trait. (Dorland, 27th ed) A deficiency of blood coagulation FACTOR XIII or fibrin stabilizing factor (FSF) that prevents blood clot formation and results in a clinical hemorrhagic diathesis. A deficiency or absence of fibrinogen (coagulation factor I) in the blood. (Dorland, 27th ed) Absence or reduced levels of prothrombin in the blood. An absence or reduced level of blood coagulation factor XII. It normally occurs in the absence of patient or family history of hemorrhagic disorders and is marked by prolonged clotting time. An autosomal recessive characteristic or a coagulation disorder acquired in association with VITAMIN K DEFICIENCY. FACTOR VII is a Vitamin K dependent glycoprotein essential to the extrinsic pathway of coagulation. Blood coagulation disorder usually inherited as an autosomal recessive trait, though it can be acquired. It is characterized by defective activity in both the intrinsic and extrinsic pathways, impaired thromboplastin time, and impaired prothrombin consumption. 286.3 is a specific code that can be used to specify a diagnosis 286.3 contains 56 index entries View the ICD-9-CM Volume 1 286.* hierarchy 286.3 also known as: 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 Index entries containing 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 coagulation (factor) (see also Deficiency, coagulation factor) 286.9 specified type NEC 286.3 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 C (see also Defect, coagulation) 286.3 coagulation factor NEC 286.9 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 X (congenital) (Stuart-Prower) 286.3 XII (congenital) (Hageman) 286.3 XIII (congenital) (fibrin stabilizing) 286.3 hageman 286.3 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