D68.2 is the authoritative medical code for Hereditary deficiency of other clotting factors. This classification is used in medical billing and clinical recording to specify the clinical criteria for hereditary deficiency of other clotting factors (ICD-10-CM D68.2), ensuring healthcare documentation aligns with 2026 federal coding standards.
Billing Status: YES. This is a valid, specific, and billable ICD-10-CM reference.
Official Registry Overview & Definition
Hereditary deficiency of other clotting factors is a billable ICD-10-CM diagnosis code D68.2. Inclusion terms: 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. Excludes1 (not coded here): 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).
Official Tabular Instructional Notes
Sequencing, inclusion, and exclusion notes published for D68.2 in the official ICD-10-CM tabular list.
Inclusion Terms
Alternative terms the tabular list files under this code.
- 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
Excludes1 — Not Coded Here
Conditions that can never be reported with this code; the two are mutually exclusive.
- abnormal coagulation profile NOS R79.1
Excludes2 — Not Included Here
Conditions not covered by this code, but which may be reported alongside it when both are present.
- 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)
Frequently Asked Questions (FAQ) & Clinical Guidance
What can't be coded together with D68.2?
Per Excludes1 instructions, D68.2 must not be reported with: abnormal coagulation profile NOS (R79.1).
Can D68.2 be reported alongside related conditions?
Per Excludes2 instructions, D68.2 and the following may both be reported when both are present: 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).
What conditions are included under D68.2?
Hereditary deficiency of other clotting factors includes: AC globulin deficiency; Congenital afibrinogenemia; Deficiency of factor I [fibrinogen]; Deficiency of factor II [prothrombin]; Deficiency of factor V [labile].
Codes in This Family (31)
Official ICD-10-CM classifications in the same code family as D68.2, with their registry titles.
- D68 — Other coagulation defects
- D68.0 — Von Willebrand disease
- D68.00 — Von Willebrand disease, unspecified
- D68.01 — Von Willebrand disease, type 1
- D68.02 — Von Willebrand disease, type 2
- D68.020 — Von Willebrand disease, type 2A
- D68.021 — Von Willebrand disease, type 2B
- D68.022 — Von Willebrand disease, type 2M
- D68.023 — Von Willebrand disease, type 2N
- 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
- D68.3 — 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
- D68.32 — Hemorrhagic disorder due to extrinsic circulating anticoagulants
- D68.4 — Acquired coagulation factor deficiency
- D68.5 — Primary thrombophilia
- D68.51 — Activated protein C resistance
- D68.52 — Prothrombin gene mutation
- D68.59 — Other primary thrombophilia
- D68.6 — Other thrombophilia
- D68.61 — Antiphospholipid syndrome
- D68.62 — Lupus anticoagulant syndrome
- D68.69 — Other thrombophilia
- D68.8 — Other specified coagulation defects
- D68.9 — Coagulation defect, unspecified
Indexed Clinical Terms (51)
Clinical term phrases from the official ICD-10-CM Index to Diseases and Injuries that map to this code.
- 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, AC globulin (congenital) (hereditary)
- Deficiency, deficient, accelerator globulin (Ac G) (blood)
- Deficiency, deficient, activating factor (blood)
- Deficiency, deficient, autoprothrombin, C
- Deficiency, deficient, autoprothrombin, I
- 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)
- Syndrome, Owren's
Related Codes & Numerical Sequence (Crawl Map)
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