D68.59

Billable

Other primary thrombophilia

Other primary thrombophilia

Status

Billable / Specific

Block

D65-D69

Parent Code

D68.5

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

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

Excludes 1

Codes that cannot be used together with this code (mutual exclusion)

Excludes 2

Conditions not included here, but the patient may have both

Related Codes(2)
D68.51

Activated protein C resistance

BillableD68.52

Prothrombin gene mutation

Billable
Also Known As / Clinical Terms(228)

SNOMED CT

UMLS

Clinical Terms

  • Anti-thrombin III deficiency
  • Antithrombin III Deficiency
  • DEFIC PROTEIN S
  • Reduced antithrombin III activity
  • PROTEIN C DEFIC
  • Hypercoagulation
  • Antithrombin 3 Deficiency
  • Acquired protein C deficiency
  • Deficiencies, Protein S
  • Protein S Deficiency Disease
  • DEFIC PROTEIN C
  • Elevated fibrinogen level
  • AT (antithrombin) deficiency
  • Antithrombin 3 Deficiencies
  • Protein S deficiency disease (disorder)
  • Hypercoagulability state (finding)
  • Thrombophilia (disorder)
  • thrombophilia
  • Decreased antithrombin III
  • Protein C deficiency disease (disorder)
  • protein c deficiency
  • Protein S Deficiencies
  • Acquired AT (antithrombin) deficiency
  • Hypercoagulable state
  • Hereditary hyperfibrinogenaemia
  • Reduced protein C activity
  • Antithrombin deficiency
  • Congenital hyperfibrinogenemia
  • Cerebral ischemic stroke due to hypercoagulable state
  • Excessive Blood Clotting
  • Deficiencies, Antithrombin III
  • Deficiencies, Protein C
  • Hereditary hyperfibrinogenemia
  • Protein S Deficiency
  • Acquired antithrombin deficiency
  • DEFIC ANTITHROMBIN III
  • THPH7
  • THROMBOPHILIA DUE TO ANTITHROMBIN III DEFICIENCY
  • Heparin cofactor II deficiency
  • antithrombin deficiencies
  • s protein deficiency
  • Protein C deficiency disease
  • Hereditary thrombophilia
  • Heterozygous protein C deficiency
  • Hyperfibrinogenaemia
  • c deficiency protein
  • Hereditary Thrombophilia Due To Protein S Deficiency
  • Acquired antithrombin 3 deficiency
  • Hereditary heparin cofactor II deficiency
  • thrombophilias
  • hypercoagulable states
  • AT3D
  • Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
  • Hyperfibrinogenemia
  • Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency
  • Upper gastrointestinal hemorrhage associated with hypercoagulability state
  • Hypercoagulabilities
  • Antithrombin III deficiency (disorder)
  • Thrombophilia NOS
  • Blood hyperviscosity
  • Congenital hyperfibrinogenaemia
  • Deficiencies, Antithrombin 3
  • Thrombotic tendency observations
  • Primary thrombophilia NEC
  • Hereditary antithrombin III deficiency
  • ANTITHROMBIN 3 DEFIC
  • Deficiency, Protein C
  • Hereditary hypercoagulable disorder
  • Hereditary elevated factor XI
  • Hypercoagulable state NOS
  • Hypercoagulability state
  • Protein C Deficiencies
  • Upper gastrointestinal haemorrhage associated with hypercoagulability state
  • Homozygous protein C deficiency
  • Deficiency, Antithrombin III
  • deficiency protein c
  • hypercoagulability states
  • Homozygous protein S deficiency
  • Hereditary protein S deficiency
  • Primary thrombophilia
  • Deficiency, Antithrombin 3
  • hypercoagulability
  • Acquired antithrombin III deficiency
  • Antithrombin III Deficiencies
  • Hereditary Thrombophilia Due To Protein C Deficiency
  • Acquired protein S deficiency
  • deficiency protein s
  • Heterozygous protein S deficiency
  • Deficiency, Protein S
  • Acquired heparin cofactor II deficiency
  • Primary hypercoagulable state NEC
  • Hereditary protein C deficiency
  • Fibrinogen in blood above reference range
  • ANTITHROMBIN III DEFIC
  • PROTEIN S DEFIC
  • c protein deficiency
  • Hereditary elevated factor VIII
  • Cerebral ischaemic stroke due to hypercoagulable state
Frequently Asked Questions
What is the ICD-10 code for other primary thrombophilia?

The ICD-10-CM code for other primary thrombophilia is D68.59. The full clinical description is "Other primary thrombophilia". D68.59 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code D68.59 mean?

ICD-10-CM code D68.59 represents “Other primary thrombophilia”. It is classified under Chapter 3: Diseases of the Blood and Blood-Forming Organs and is a billable/specific code that can be used on a claim.

Is D68.59 a billable code?

Yes, D68.59 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is D68.59 in?

D68.59 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).

What codes cannot be used with D68.59?

D68.59 has Excludes1 notes indicating codes that cannot be used together with it, including: abnormal coagulation profile NOS (R79.1); antiphospholipid syndrome (D68.61); lupus anticoagulant (D68.62); and 7 more.

What SNOMED CT codes does D68.59 map to?

D68.59 maps to 29 SNOMED CT concepts: 36351005, 1196942001, 1217411000, 1217410004, 1217409009, and 24 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for D68.59?

D68.59 is linked to 7 UMLS Concept Unique Identifiers: C0272375, C0398623, C0398625, C0242666, C2873799, and 2 more. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does D68.59 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other primary thrombophilia affect a person's functioning: body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of D68.59?

There is no direct ICD-11 mapping available for D68.59 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.

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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.