D68.59
BillableOther primary thrombophilia
Other primary thrombophilia
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)
- abnormal coagulation profile NOS (R79.1)
- antiphospholipid syndrome (D68.61)
- lupus anticoagulant (D68.62)
- secondary activated protein C resistance (D68.69)
- secondary antiphospholipid antibody syndrome (D68.69)
- secondary lupus anticoagulant with hypercoagulable state (D68.69)
- secondary systemic lupus erythematosus [SLE] inhibitor with hypercoagulable state (D68.69)
- systemic lupus erythematosus [SLE] inhibitor finding without diagnosis (R76.0)
- systemic lupus erythematosus [SLE] inhibitor with hemorrhagic disorder (D68.312)
- thrombotic thrombocytopenic purpura (M31.19)
Excludes 2
Conditions not included here, but the patient may have both
- 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)
- 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)
Also Known As / Clinical Terms
SNOMED CT
- Protein S deficiency1563006
- Protein S deficiency disease1563006
- AT (antithrombin) deficiency36351005
- Antithrombin 3 deficiency36351005
- Antithrombin III deficiency36351005
- Antithrombin deficiency36351005
- Protein C deficiency76407009
- Protein C deficiency disease76407009
- Hypercoagulability76612001
- Hypercoagulability state76612001
- Hypercoagulable state76612001
- Elevated fibrinogen level123791008
- Fibrinogen in blood above reference range123791008
- Thrombophilia234467004
- Heparin cofactor II deficiency234468009
- Thrombotic tendency observations250356000
- Upper gastrointestinal haemorrhage associated with hypercoagulability state430349003
- Upper gastrointestinal hemorrhage associated with hypercoagulability state430349003
- Hyperfibrinogenaemia439000005
- Hyperfibrinogenemia439000005
- Hereditary protein C deficiency439274008
- Hereditary hypercoagulable disorder439698008
- Hereditary thrombophilia439698008
- Primary thrombophilia439698008
- Hereditary antithrombin III deficiency439699000
- Hereditary heparin cofactor II deficiency439701000
- Hereditary protein S deficiency439702007
- Congenital hyperfibrinogenaemia440924009
- Congenital hyperfibrinogenemia440924009
- Hereditary hyperfibrinogenaemia440924009
- Hereditary hyperfibrinogenemia440924009
- Heterozygous protein S deficiency440988005
- Hereditary elevated factor XI441001005
- Hereditary elevated factor VIII441042008
- Heterozygous protein C deficiency441101007
- Homozygous protein C deficiency441188004
- Homozygous protein S deficiency441189007
- Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency724344004
- Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency783250007
- Cerebral ischaemic stroke due to hypercoagulable state788883008
- Cerebral ischemic stroke due to hypercoagulable state788883008
- Acquired AT (antithrombin) deficiency1196942001
- Acquired antithrombin 3 deficiency1196942001
- Acquired antithrombin III deficiency1196942001
- Acquired antithrombin deficiency1196942001
- Acquired protein S deficiency1217409009
- Acquired protein C deficiency1217410004
- Acquired heparin cofactor II deficiency1217411000
UMLS
- ANTITHROMBIN 3 DEFICC0272375
- ANTITHROMBIN III DEFICC0272375
- ANTITHROMBIN III DEFICIENCYC0272375
- AT (antithrombin) deficiencyC0272375
- AT3DC0272375
- Anti-thrombin III deficiencyC0272375
- Antithrombin 3 DeficienciesC0272375
- Antithrombin 3 DeficiencyC0272375
- Antithrombin 3 deficiencyC0272375
- Antithrombin III DeficienciesC0272375
- Antithrombin III DeficiencyC0272375
- Antithrombin III deficiencyC0272375
- Antithrombin III deficiency (disorder)C0272375
- Antithrombin deficiencyC0272375
- DEFIC ANTITHROMBIN IIIC0272375
- Decreased antithrombin IIIC0272375
- Deficiencies, Antithrombin 3C0272375
- Deficiencies, Antithrombin IIIC0272375
- Deficiency, Antithrombin 3C0272375
- Deficiency, Antithrombin IIIC0272375
- Reduced antithrombin III activityC0272375
- THPH7C0272375
- THROMBOPHILIA DUE TO ANTITHROMBIN III DEFICIENCYC0272375
- antithrombin 3 deficiencyC0272375
- antithrombin deficienciesC0272375
- antithrombin deficiencyC0272375
- antithrombin iii deficiencyC0272375
- Blood hyperviscosityC0398623
- Excessive Blood ClottingC0398623
- HypercoagulabilitiesC0398623
- HypercoagulabilityC0398623
- Hypercoagulability stateC0398623
- Hypercoagulability state (finding)C0398623
- Hypercoagulable stateC0398623
- Hypercoagulable state NOSC0398623
- HypercoagulationC0398623
- ThrombophiliaC0398623
- Thrombophilia (disorder)C0398623
- Thrombophilia NOSC0398623
- ThrombophiliasC0398623
- hypercoagulabilityC0398623
- hypercoagulability statesC0398623
- hypercoagulable stateC0398623
- hypercoagulable statesC0398623
- hypercoagulationC0398623
- thrombophiliaC0398623
- thrombophiliasC0398623
- DEFIC PROTEIN CC0398625
- Deficiencies, Protein CC0398625
- Deficiency, Protein CC0398625
- Hereditary Thrombophilia Due To Protein C DeficiencyC0398625
- PROTEIN C DEFICC0398625
- Protein C DeficienciesC0398625
- Protein C DeficiencyC0398625
- Protein C Deficiency DiseaseC0398625
- Protein C deficiencyC0398625
- Protein C deficiency diseaseC0398625
- Protein C deficiency disease (disorder)C0398625
- Reduced protein C activityC0398625
- c deficiency proteinC0398625
- c protein deficiencyC0398625
- deficiency protein cC0398625
- protein c deficiencyC0398625
- DEFIC PROTEIN SC0242666
- Deficiencies, Protein SC0242666
- Deficiency, Protein SC0242666
- Hereditary Thrombophilia Due To Protein S DeficiencyC0242666
- Hereditary thrombophilia due to protein S deficiencyC0242666
- PROTEIN S DEFICC0242666
- Protein S DeficienciesC0242666
- Protein S DeficiencyC0242666
- Protein S Deficiency DiseaseC0242666
- Protein S deficiencyC0242666
- Protein S deficiency diseaseC0242666
- Protein S deficiency disease (disorder)C0242666
- deficiency protein sC0242666
- protein s deficienciesC0242666
- protein s deficiencyC0242666
- s protein deficiencyC0242666
- Other primary thrombophiliaC2873799
- Primary hypercoagulable state NECC2873797
- Primary thrombophilia NECC2873798
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.
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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.