Diagnosis Code: 286.3

Short Description: Cong def clot factor NEC

Long Description: Congenital deficiency of other clotting factors

Code Classification:

• Diseases of the blood and blood-forming organs (280–289)
  • Diseases of the blood and blood-forming organs (280-289)
    • 286 Coagulation defects
      • 286.3 Cong def clot factor NEC

Code Version: 2015 ICD-9-CM

Synonyms

• 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

References to Index of Diseases and Injuries

The code 286.3 has the following ICD-9-CM references to the Index of Diseases and Injuries

• 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
    • 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

• Hemiathetosis 781.0

• 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

Crosswalk Information

The code 286.3 converts into the following ICD-10 code(s):

Similar Codes

This page was last updated on: 10/1/2014

« Previous Code