Reserved for future guideline expansion
D68.4
Acquired coagulation factor deficiency
Billable FY2026 2025-10-01 → 2026-09-30
Exclusions 13 never code together
D68code
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 notes 2
D68.4code
Inclusion terms
- Deficiency of coagulation factor due to liver disease
- Deficiency of coagulation factor due to vitamin K deficiency
Official Guidelines 1 names this code
ICD-10-CM Official Guidelines for Coding and Reporting, quoted in full. Published by CMS and NCHS; in the public domain.
Index entries leading here 6
- Deficiency, deficient
- AC globulin (congenital) (hereditary) D68.2
- acquired D68.4
- factor — see also Deficiency, coagulation
- fibrin-stabilizing factor (congenital) (hereditary) D68.2
- acquired D68.4
- labile factor (congenital) (hereditary) D68.2
- acquired D68.4
- proaccelerin (congenital) (hereditary) D68.2
- acquired D68.4
- proconvertin factor (congenital) (hereditary) D68.2
- acquired D68.4
- prothrombin (congenital) (heredItary) D68.2
- acquired D68.4
- stable factor (congenital) (hereditary) D68.2
- acquired D68.4
- coagulation NOS D68.9
- AC globulin (congenital) (hereditary) D68.2
- Hypoprothrombinemia (congenital) (hereditary) (idiopathic) D68.2
- acquired D68.4
- Fibrinopenia (hereditary) D68.2
- acquired D68.4
- Defect, defective Q89.9
- Hemophilia (classical) (familial) (hereditary) D66
- Hyperprothrombinemia, causing coagulation factor deficiency D68.4
Alongside this code 8 same parent — D68
D68.0 Von Willebrand disease category D68.1 Hereditary factor XI deficiency D68.2 Hereditary deficiency of other clotting factors D68.3 Hemorrhagic disorder due to circulating anticoagulants category D68.5 Primary thrombophilia category D68.6 Other thrombophilia category D68.8 Other specified coagulation defects D68.9 Coagulation defect, unspecified
Medications 1
MED-RT files conditions by MeSH, which carves the world differently from ICD-10. These are name matches on this code's description, offered as candidates — not as an assertion that they are this code.
Additional references
AHA Coding Clinic® Licence required
Official coding advice for this code. Published by the American Hospital Association. Not included in this installation.