ICD-10 Diagnosis Code D68.2

Hereditary deficiency of other clotting factors

Diagnosis Code D68.2

ICD-10: D68.2
Short Description: Hereditary deficiency of other clotting factors
Long Description: Hereditary deficiency of other clotting factors
This is the 2018 version of the ICD-10-CM diagnosis code D68.2

Valid for Submission
The code D68.2 is valid for submission for HIPAA-covered transactions.

Code Classification
  • Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50–D89)
    • Coagulation defects, purpura and other hemorrhagic conditions (D65-D69)
      • Other coagulation defects (D68)

Information for Medical Professionals

Convert to ICD-9 Additional informationCallout TooltipGeneral Equivalence Map
The ICD-10 and ICD-9 GEMs are used to facilitate linking between the diagnosis codes in ICD-9-CM and the new ICD-10-CM code set. The GEMs are the raw material from which providers, health information vendors and payers can derive specific applied mappings to meet their needs.
  • 286.3 - Cong def clot factor NEC

  • Acquired coagulation factor inhibitor disorder
  • Alpha chain defect dysfibrinogenemia
  • Autosomal dominant deficiency of plasminogen
  • Beta chain defect dysfibrinogenemia
  • Congenital afibrinogenemia
  • Congenital fibrinogen abnormality
  • Contact factor deficiency
  • Drug-induced coagulation inhibitor disorder
  • Dysfibrinogenemia
  • Dysplasminogenemia
  • 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
  • Fibrinolytic bleeding syndrome
  • Gamma chain defect dysfibrinogenemia
  • Hemorrhagic disease of the newborn due to factor II deficiency
  • Heparin cofactor II deficiency
  • Hereditary dysfibrinogenemia
  • Hereditary dysplasminogenemia
  • 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 B subunit deficiency
  • Hereditary factor XIII deficiency disease
  • Hereditary hypoplasminogenemia
  • Hereditary thrombophilic dysfibrinogenemia
  • High molecular weight kininogen deficiency
  • Hyperfibrinogenemia
  • Hypodysfibrinogenemia
  • Hypoplasminogenemia
  • Passovoy factor deficiency
  • Platelet factor V deficiency
  • Platelet procoagulant activity deficiency
  • Prekallikrein deficiency
  • Prothrombin complex deficiency

Index of Diseases and Injuries
References found for the code D68.2 in the Index of Diseases and Injuries:

Information for Patients

Bleeding Disorders

Also called: Clotting disorders

Normally, if you get hurt, your body forms a blood clot to stop the bleeding. For blood to clot, your body needs cells called platelets and proteins known as clotting factors. If you have a bleeding disorder, you either do not have enough platelets or clotting factors or they don't work the way they should.

Bleeding disorders can be the result of other diseases, such as severe liver disease or a lack of vitamin K. They can also be inherited. Hemophilia is an inherited bleeding disorder. Bleeding disorders can also be a side effect of medicines such as blood thinners.

Various blood tests can check for a bleeding disorder. You will also have a physical exam and history. Treatments depend on the cause. They may include medicines and transfusions of blood, platelets, or clotting factor.

  • Bleeding disorders (Medical Encyclopedia)
  • Bleeding time (Medical Encyclopedia)
  • Disseminated intravascular coagulation (DIC) (Medical Encyclopedia)
  • Partial thromboplastin time (PTT) (Medical Encyclopedia)
  • Prothrombin time (PT) (Medical Encyclopedia)

[Read More]

Prothrombin deficiency Prothrombin deficiency is a bleeding disorder that slows the blood clotting process. People with this condition often experience prolonged bleeding following an injury, surgery, or having a tooth pulled. In severe cases of prothrombin deficiency, heavy bleeding occurs after minor trauma or even in the absence of injury (spontaneous bleeding). Women with prothrombin deficiency can have prolonged and sometimes abnormally heavy menstrual bleeding. Serious complications can result from bleeding into the joints, muscles, brain, or other internal organs. Milder forms of prothrombin deficiency do not involve spontaneous bleeding, and the condition may only become apparent following surgery or a serious injury.
[Read More]

Factor X deficiency Factor X deficiency is a rare bleeding disorder that varies in severity among affected individuals. The signs and symptoms of this condition can begin at any age, although the most severe cases are apparent in childhood. Factor X deficiency commonly causes nosebleeds, easy bruising, bleeding under the skin, bleeding of the gums, blood in the urine (hematuria), and prolonged or excessive bleeding following surgery or trauma. Women with factor X deficiency can have heavy or prolonged menstrual bleeding (menorrhagia) or excessive bleeding in childbirth, and may be at increased risk of pregnancy loss (miscarriage). Bleeding into joint spaces (hemarthrosis) occasionally occurs. Severely affected individuals have an increased risk of bleeding inside the skull (intracranial hemorrhage), in the lungs (pulmonary hemorrhage), or in the gastrointestinal tract, which can be life-threatening.
[Read More]
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