ICDcodes.org
FY2027

D68.2 — Hereditary deficiency of other clotting factors

BillableCC

Is D68.2 billable?

Yes — D68.2 is billable for FY2027. D68.2 is a valid, billable ICD-10-CM code at the highest level of specificity in its branch. D68.2 may be submitted for encounters from October 1, 2026 through September 30, 2027.

D68.2 at a glance

CodeD68.2
DescriptionHereditary deficiency of other clotting factors
BillableYes
Code setICD-10-CM FY2027
Valid for encountersOctober 1, 2026 – September 30, 2027

Which MS-DRGs does D68.2 group to?

D68.2 sits in MDC 16 and helps define the logic of 1 MS-DRG (version 44, FY2027). Which one a stay actually groups to also depends on procedures and secondary diagnoses.

  • 813Coagulation Disordersmedical

As a secondary diagnosis, D68.2 is a complication or comorbidity (CC), which can move a stay into a higher-paying DRG.

How is D68.2 listed in the Alphabetic Index?

These are the routes through the Alphabetic Index that lead to D68.2. They show the wording a clinician may have documented, which often differs from the Tabular description.

  • Dysfibrinogenemia (congenital)
  • Fibrinopenia (hereditary)
  • Hageman's factor defect, deficiency or disease
  • 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)
  • Absence › fibrinogen (of) (organ or part) (complete or partial)
  • Afibrinogenemia › congenital
  • Defect, defective › fibrin polymerization

Inclusion terms

Alternative wording in documentation that is classified to D68.2.

  • 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 — never code together — inherited from D68

The conditions below can never be reported together with D68.2 on the same claim. An Excludes1 note means the two conditions cannot occur in the same patient, so reporting both is a coding error.

  • abnormal coagulation profile NOS (R79.1)

Excludes2 — not included here — inherited from Chapter 3

The conditions below are not part of D68.2, but a patient may have both at the same time. When documentation supports it, D68.2 and the excluded code may both be reported.

  • autoimmune disease (systemic) NOS (M35.9)
  • certain conditions originating in the perinatal period (P00-P96)
  • complications of pregnancy, childbirth and the puerperium (O00-O9A)
  • congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
  • endocrine, nutritional and metabolic diseases (E00-E88)
  • human immunodeficiency virus [HIV] disease (B20)
  • injury, poisoning and certain other consequences of external causes (S00-T88)
  • neoplasms (C00-D49)
  • symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)

Excludes2 — not included here — inherited from D68

The conditions below are not part of D68.2, but a patient may have both at the same time. When documentation supports it, D68.2 and the excluded code may both be reported.

  • 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)

How long has D68.2 existed?

D68.2 has been in ICD-10-CM since at least FY2016, the earliest fiscal year on record here.

Derived from the official order files for FY2016–FY2026. FY2017 and FY2020 publish no order file, so those years are not covered.

Which conditions are coded to D68.2?

What other codes are in the D68 family? (8)