2026 ICD-10-CM Diagnosis Code D68.59Other primary thrombophilia

ICD-10-CM CodesD50–D89D65-D69D68

ICD-10-CM D68.59
CMSSource: CMS FY 2026 ICD-10-CM dataset · Effective Oct 1, 2025 – Sep 30, 2026

D68.59 is a billable ICD-10-CM diagnosis code for other primary thrombophilia. It is valid on HIPAA claims for fiscal year 2026 (October 1, 2025 through September 30, 2026) and groups to MS-DRG 814 through 816. In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Coagulation and hemorrhagic disorders.

Code Identity

ICD-10-CM Code
D68.59
Billable Status
Yes — Valid for Submission
Code Describes
Other primary thrombophilia
Short Description
Other primary thrombophilia
Same as the full description in the CMS dataset.
Parent Code
Primary thrombophilia

Code Classification

ChapterD50–D89Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
SectionD65-D69Coagulation defects, purpura and other hemorrhagic conditions
CategoryD68Other coagulation defects
This CodeD68.59Other primary thrombophilia

Approximate SynonymsGuidance

Alternate terms and clinical phrases that map to this code.

  • Acquired antithrombin III deficiency
  • Acquired heparin cofactor II deficiency
  • Acquired protein C deficiency
  • Acquired protein S deficiency
  • Antithrombin III deficiency
  • Cerebral ischemic stroke due to hypercoagulable state
  • Fibrinogen in blood above reference range
  • Heparin cofactor II deficiency
  • Hereditary antithrombin III deficiency
  • Hereditary elevated factor VIII
  • Hereditary elevated factor XI
  • Hereditary heparin cofactor II deficiency
  • Hereditary hyperfibrinogenemia
  • Hereditary protein C deficiency
  • Hereditary protein S deficiency
  • Hereditary thrombophilia
  • Hereditary thrombophilia due to congenital histidine-rich glycoprotein deficiency
  • Heterozygous protein C deficiency
  • Heterozygous protein S deficiency
  • Homozygous protein C deficiency
  • Homozygous protein S deficiency
  • Hypercoagulability state
  • Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency
  • Hyperfibrinogenemia
  • Protein C deficiency disease
  • Protein S deficiency disease
  • Thrombophilia
  • Thrombotic tendency observations
  • Upper gastrointestinal hemorrhage associated with hypercoagulability state

Tabular List NotesGuidance

Coding notes and annotation back-references applicable to this code.

Inclusion Terms

  • Antithrombin III deficiency
  • Hypercoagulable state NOS
  • Primary hypercoagulable state NEC
  • Primary thrombophilia NEC
  • Protein C deficiency
  • Protein S deficiency
  • Thrombophilia NOS

Index to Diseases and InjuriesGuidance

Alphabetical index entries that point to this code.

External Cause of Injuries IndexGuidance

References for this code in the External Cause of Injuries Index.

    • Deficiency, deficient
      • antithrombin (antithrombin III)
    • Deficiency, deficient
      • protein
        • C
    • Deficiency, deficient
      • protein
        • S
    • Hypercoagulable(state)
    • Hypercoagulable(state)
      • antithrombin (III) deficiency
    • Hypercoagulable(state)
      • primary NEC
    • Hypercoagulable(state)
      • protein C deficiency
    • Hypercoagulable(state)
      • protein S deficiency
    • Hypercoagulation(state)
    • Thrombophilia
    • Thrombophilia
      • primary NEC

Clinical ClassificationClinical

AHRQ’s CCSR groups this code into broader clinical categories.

CCSR BLD006
Coagulation and hemorrhagic disorders
Default principal diagnosis: inpatient Yes · outpatient Yes

Clinical InformationClinical

  • Thrombophilia

    a disorder of hemostasis in which there is a tendency for the occurrence of thrombosis.
  • Antithrombin III Deficiency

    an absence or reduced level of antithrombin iii leading to an increased risk for thrombosis.
  • Antithrombin III Deficiency

    a rare disorder characterized by the presence of low levels of antithrombin iii which prohibits the formation of blood clots. it may be inherited, usually in an autosomal dominant pattern, or acquired. it may lead to venous thrombosis and pulmonary embolism.

Patient EducationClinical

Bleeding Disorders

Normally, if you get hurt, your body forms a blood clot to stop the bleeding. For blood to clot, your body needs cells called platelets and proteins known as clotting factors. If you have a bleeding disorder, you either do not have enough platelets or clotting factors or they don't work the way they should.

Read the full article at MedlinePlus

Courtesy of MedlinePlus, a service of the U.S. National Library of Medicine.

Convert D68.59 to ICD-9-CMHistory

The closest ICD-9-CM equivalents under the General Equivalence Mappings.

ICD-9-CM
289.81 Prim hypercoagulable st
Approximate The match is approximate rather than exact.

Code HistoryHistory

FY 2016AddedAdded to the ICD-10-CM code setEffective October 1, 2015, the first year of ICD-10-CM.
FY 2017–2025No changes
FY 2026CurrentCurrent code set, no changesEffective October 1, 2025 through September 30, 2026.

Questions About D68.59Overview

Is D68.59 (Primary thrombophilia) a billable code?

Yes. This is a billable ICD-10-CM code, specific enough to report other primary thrombophilia on HIPAA-covered claims from October 1, 2025 through September 30, 2026.

What MS-DRG does D68.59 group to?

When other primary thrombophilia is the principal diagnosis on an inpatient stay, it groups to MS-DRG 814, 815, 816, with relative weights from 0.6320 to 2.1267 depending on complications. Higher weights mean higher Medicare reimbursement.

What is the ICD-9 equivalent of D68.59?

Under the General Equivalence Mappings, other primary thrombophilia converts to ICD-9-CM 289.81 (prim hypercoagulable st). The mapping is approximate, so confirm the match fits the documentation.

Footnotes

[1] Chronic - a chronic condition code indicates a condition lasting 12 months or longer and its effect on the patient based on one or both of the following criteria:

  • The condition results in the need for ongoing intervention with medical products,treatment, services, and special equipment
  • The condition places limitations on self-care, independent living, and social interactions.