All ICD10 Codes

D68

Non-Billable
ChapterD50–D89
Rankcategory
Official Description

Other coagulation defects

Use a more specific code (5 billable, 4 non-billable)
D68.0Von Willebrand diseasehas subcodesD68.1Hereditary factor XI deficiencyD68.2Hereditary deficiency of other clotting factorsD68.3Hemorrhagic disorder due to circulating anticoagulantshas subcodesD68.4Acquired coagulation factor deficiencyD68.5Primary thrombophiliahas subcodesD68.6Other thrombophiliahas subcodesD68.8Other specified coagulation defectsD68.9Coagulation defect, unspecified
Metadata & Insights
  • •Non-billable category (requires more specific sub-code).
  • •Chapter 3: Diseases of the Blood and Blood-Forming Organs (D50-D89).

CH3 Parent Instructions

Excludes2(Not included here. Code separately if applicable.)
  • 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)

Instructional Notes

Excludes1(Not coded here. Use a different code.)
  • abnormal coagulation profile NOS (R79.1)
Excludes2(Not included here. Code separately if applicable.)
  • 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)

Clinical Hierarchy

BillableHas subcodes
CH3Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89)
D65-D69Coagulation defects, purpura and other hemorrhagic conditions (D65-D69)
D68Other coagulation defectsNot billable
D68.0Von Willebrand diseaseSubcodes
D68.1Hereditary factor XI deficiencyBillable
D68.2Hereditary deficiency of other clotting factorsBillable
D68.3Hemorrhagic disorder due to circulating anticoagulantsSubcodes
D68.4Acquired coagulation factor deficiencyBillable
D68.5Primary thrombophiliaSubcodes
D68.6Other thrombophiliaSubcodes
D68.8Other specified coagulation defectsBillable
D68.9Coagulation defect, unspecifiedBillable

Applicable Ancestor Context

The following parent sections contain instructions or notes that apply to D68:

chapterCH3
Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89)
View context instructions

MS-DRG Classification

2026

No direct MS-DRG triggers identified.

Cross Reference

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