D68.2 Hereditary deficiency of other clotting factors

Billable ICD-10-CM code, FY2026. Acts as a Complication or Comorbidity (CC) as a secondary diagnosis.

Applicable to

• AC globulin deficiency
• Congenital afibrinogenemia
• Deficiency of factor I [fibrinogen]
• Deficiency of factor II [prothrombin]
• Deficiency of factor V [labile]
• Deficiency of factor VII [stable]
• Deficiency of factor X [Stuart-Prower]
• Deficiency of factor XII [Hageman]
• Deficiency of factor XIII [fibrin stabilizing]
• Dysfibrinogenemia (congenital)
• Hypoproconvertinemia
• Owren's disease
• Proaccelerin deficiency

Applies from D68 Other coagulation defects

Excludes1 (never code together)

• abnormal coagulation profile NOS (R79.1)

Excludes2 (not included here)

• coagulation defects complicating abortion or ectopic or molar pregnancy (O00-O07, O08.1)
• coagulation defects complicating pregnancy, childbirth and the puerperium (O45.0, O46.0, O67.0, O72.3)

Risk adjustment (HCC)

• CMS-HCC V28: HCC 112 — Immune Thrombocytopenia and Specified Coagulation Defects and Hemorrhagic Conditions
• CMS-HCC V22: HCC 48 — Coagulation Defects and Other Specified Hematological Disorders
• ESRD V24: HCC 48

MS-DRG index

Defines the logic of DRG(s) 813 in MDC 16.

Approximate ICD-9-CM (GEMs)

• 286.3 Congenital deficiency of other clotting factors

Code annotations containing back-references to D68.2

Back-references to D68

• Type 1 Excludes: R79.1 Abnormal coagulation profile ("coagulation defects (D68.-)")

Diagnosis Index entries for D68.2

• Absence (of) (organ or part) (complete or partial) › fibrinogen (congenital)
• Afibrinogenemia › congenital
• Defect, defective › coagulation (factor) › hereditary NEC
• Defect, defective › fibrin polymerization
• Defect, defective › Hageman (factor)
• Deficiency, deficient › accelerator globulin (Ac G) (blood)
• Deficiency, deficient › AC globulin (congenital) (hereditary)
• Deficiency, deficient › activating factor (blood)
• Deficiency, deficient › autoprothrombin › I
• Deficiency, deficient › autoprothrombin › C
• Deficiency, deficient › clotting factor NEC (hereditary)
• Deficiency, deficient › coagulation NOS › clotting factor NEC
• Deficiency, deficient › contact factor
• Deficiency, deficient › factor › Hageman
• Deficiency, deficient › factor › I (congenital) (hereditary)
• Deficiency, deficient › factor › II (congenital) (hereditary)
• Deficiency, deficient › factor › V (congenital) (hereditary)
• Deficiency, deficient › factor › VII (congenital) (hereditary)
• Deficiency, deficient › factor › X (congenital) (hereditary)
• Deficiency, deficient › factor › XII (congenital) (hereditary)
• Deficiency, deficient › factor › XIII (congenital) (hereditary)
• Deficiency, deficient › fibrin-stabilizing factor (congenital) (hereditary)
• Deficiency, deficient › fibrinase
• Deficiency, deficient › fibrinogen (congenital) (hereditary)
• Deficiency, deficient › glass factor
• Deficiency, deficient › Hageman factor
• Deficiency, deficient › labile factor (congenital) (hereditary)
• Deficiency, deficient › Laki-Lorand factor
• Deficiency, deficient › proaccelerin (congenital) (hereditary)
• Deficiency, deficient › proconvertin factor (congenital) (hereditary)
• Deficiency, deficient › prothrombin (congenital) (heredItary)
• Deficiency, deficient › Prower factor
• Deficiency, deficient › SPCA (factor VII)
• Deficiency, deficient › stable factor (congenital) (hereditary)
• Deficiency, deficient › Stuart-Prower (factor X)
• Deficiency, deficient › thrombokinase
• Disease, diseased › Hageman (congenital factor XII deficiency)
• Disease, diseased › Stuart-Prower (congenital factor X deficiency)
• Disease, diseased › Stuart's (congenital factor X deficiency)
• Dysfibrinogenemia (congenital)
• Fibrinogenopenia › congenital
• Fibrinopenia (hereditary)
• Hageman's factor defect, deficiency or disease
• Hypofibrinogenemia › congenital (hereditary)
• Hypoproconvertinemia, congenital (hereditary)
• Hypoprothrombinemia (congenital) (hereditary) (idiopathic)
• Owren's disease or syndrome (parahemophilia)
• Parahemophilia
• Stuart deficiency disease (factor X)
• Stuart-Prower factor deficiency (factor X)

Nearby codes

• D68.029 Von Willebrand disease, type 2, unspecified
• D68.03 Von Willebrand disease, type 3
• D68.04 Acquired von Willebrand disease
• D68.09 Other von Willebrand disease
• D68.1 Hereditary factor XI deficiency
• D68.2 Hereditary deficiency of other clotting factors (this code)
• D68.3 Hemorrhagic disorder due to circulating anticoagulants
• D68.31 Hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors
• D68.311 Acquired hemophilia
• D68.312 Antiphospholipid antibody with hemorrhagic disorder
• D68.318 Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors