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D68.2

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Hereditary deficiency of other clotting factors

Filed alongside this entry 777

under Syndrome

Index entries, exactly as the book files them. This says they are listed together — not that any of them is documented in your chart.

Billable FY2027 2026-10-01 → 2027-09-30
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Everything the published sources say about one code, on one page.

  1. Read the Excludes1 block first — it is the one that stops you coding this at all alongside another code.
  2. Excludes2, Code first, Use additional and Includes follow. A note inherited from a parent category is labelled with the category it came from, so you can see why it applies.
  3. Official Guidelines sit below. "Guidelines naming this code" cite the code or a range containing it; "Chapter guidance" is the general guidance for its chapter and is the weaker signal.
  4. Guideline text is quoted verbatim with its section number and page, so you can check it against the published document.
  5. Risk-model chips show which published CMS models map this code.

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Exclusions12never code together
D68code
Excludes1
  • abnormal coagulation profile NOS (R79.1)R79.1
Excludes2
  • coagulation defects complicating abortion or ectopic or molar pregnancy (O00-O07, O08.1)O00-O07O08.1
  • coagulation defects complicating pregnancy, childbirth and the puerperium (O45.0, O46.0, O67.0, O72.3)O45.0O46.0O67.0O72.3
D50-D89chapter
Excludes2
  • autoimmune disease (systemic) NOS (M35.9)M35.9
  • certain conditions originating in the perinatal period (P00-P96)P00-P96
  • complications of pregnancy, childbirth and the puerperium (O00-O9A)O00-O9A
  • congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)Q00-Q99
  • endocrine, nutritional and metabolic diseases (E00-E88)E00-E88
  • human immunodeficiency virus [HIV] disease (B20)B20
  • injury, poisoning and certain other consequences of external causes (S00-T88)S00-T88
  • neoplasms (C00-D49)C00-D49
  • symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)R00-R94

Excludes1 — never code together. The excluded condition and this one are mutually exclusive.

Excludes2 — not included here, but the patient may have both. Code both when documented.

Instructional notes13
D68.2code
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
Official Guidelines1names this code

ICD-10-CM Official Guidelines for Coding and Reporting, quoted in full. Published by CMS and NCHS; in the public domain.

I.C.3 Chapter 3: Disease of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89) names this code p.39

Reserved for future guideline expansion

Index entries leading here17
  • Absence (of) (organ or part) (complete or partial)
    • fibrinogen (congenital) D68.2
  • Deficiency, deficient
    • accelerator globulin (Ac G) (blood) D68.2
    • AC globulin (congenital) (hereditary) D68.2
    • activating factor (blood) D68.2
    • autoprothrombin
    • coagulation NOS D68.9
      • clotting factor NEC D68.2
    • clotting factor NEC (hereditary) D68.2
    • contact factor D68.2
    • Laki-Lorand factor D68.2
    • proaccelerin (congenital) (hereditary) D68.2
    • proconvertin factor (congenital) (hereditary) D68.2
    • prothrombin (congenital) (heredItary) D68.2
    • SPCA (factor VII) D68.2
    • stable factor (congenital) (hereditary) D68.2
    • Stuart-Prower (factor X) D68.2
    • thrombokinase D68.2
    • Prower factor D68.2
    • factor — see also Deficiency, coagulation
      • Hageman D68.2
      • I (congenital) (hereditary) D68.2
      • II (congenital) (hereditary) D68.2
      • V (congenital) (hereditary) D68.2
      • VII (congenital) (hereditary) D68.2
      • X (congenital) (hereditary) D68.2
      • XII (congenital) (hereditary) D68.2
      • XIII (congenital) (hereditary) D68.2
    • fibrin-stabilizing factor (congenital) (hereditary) D68.2
    • fibrinase D68.2
    • fibrinogen (congenital) (hereditary) D68.2
    • glass factor D68.2
    • Hageman factor D68.2
    • labile factor (congenital) (hereditary) D68.2
  • Afibrinogenemia D68.8
  • Defect, defective Q89.9
    • coagulation (factor) D68.9
    • Hageman (factor) D68.2
    • fibrin polymerization D68.2
  • Fibrinogenopenia D68.8
  • Hypofibrinogenemia D68.8
    • congenital (hereditary) D68.2
  • Disease, diseased — see also Syndrome
    • Stuart's (congenital factor X deficiency) D68.2
    • Stuart-Prower (congenital factor X deficiency) D68.2
    • Hageman (congenital factor XII deficiency) D68.2
  • Dysfibrinogenemia (congenital) D68.2
  • Fibrinopenia (hereditary) D68.2
  • Hageman's factor defect, deficiency or disease D68.2
  • Hypoproconvertinemia, congenital (hereditary) D68.2
  • Hypoprothrombinemia (congenital) (hereditary) (idiopathic) D68.2
  • Syndrome — see also Disease
  • Owren's disease or syndrome (parahemophilia) D68.2
  • Parahemophilia D68.2
  • Stuart deficiency disease (factor X) D68.2
  • Stuart-Prower factor deficiency (factor X) D68.2
Alongside this code8same parent — D68
D68.0 Von Willebrand disease category D68.1 Hereditary factor XI deficiency D68.3 Hemorrhagic disorder due to circulating anticoagulants category D68.4 Acquired coagulation factor deficiency D68.5 Primary thrombophilia category D68.6 Other thrombophilia category D68.8 Other specified coagulation defects D68.9 Coagulation defect, unspecified
Additional references
AHA Coding Clinic® Licence required

Official coding advice for this code. Published by the American Hospital Association. Not included in this installation.

Risk adjustment

CMS22HCC48 CMS28HCC112 ESRD21HCC48 ESRD24HCC48 HHS08HHS_HCC075

Presence is a property of the code. Untick a model to hide it everywhere.

This code

Billable
yes
Code set
FY2027
Parent
D68
Block
D65-D69
Siblings
8

Present FY2018–FY2027.