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289.81 - Primary Hypercoagulable State


The ICD 9 Code for Primary hypercoagulable state is listed as 289.81.
Additional information concerning this code and description can be found below including ICD 10 crosswalks / GEMS, and chapter information where available.
ICD 9 CM Field Value
Diagnosis Code: 289.81
Long Description: Primary hypercoagulable state
Short Description: Prim hypercoagulable st
Chapter: Diseases Of The Blood And Blood-Forming Organs
Block: Other diseases of blood and blood-forming organs (289-289)
Related Descriptions: Catastrophic antiphospholipid syndrome
Factor V Leiden mutation
Hereditary antithrombin III deficiency
Hereditary heparin cofactor II deficiency
Hereditary protein C deficiency
Hereditary protein S deficiency
Hereditary thrombophilia
Heterozygous protein C deficiency
Heterozygous protein S deficiency
Heterozygous prothrombin G20210A mutation
Homozygous protein C deficiency
Homozygous protein S deficiency
Homozygous prothrombin G20210A mutation
Protein S deficiency disease
Prothrombin G20210A mutation
Resistance to activated protein C due to Factor V Leiden
Thrombophilia due to acquired antithrombin III deficiency
Thrombophilia due to acquired protein C deficiency
Thrombophilia due to acquired protein S deficiency
Thrombophilia due to antiphospholipid antibody
Upper gastrointestinal hemorrhage associated with hypercoagulability state
ICD-10-CM Diagnosis Codes General Equivalence Mappings (GEMS):
ICD-10-CM Code: D68.51 - Activated protein C resistance (approximate)
ICD-10-CM Code: D68.52 - Prothrombin gene mutation (approximate)
ICD-10-CM Code: D68.59 - Other primary thrombophilia (approximate)
ICD-10-CM Code: D68.61 - Antiphospholipid syndrome (approximate)
ICD-10-CM Code: D68.62 - Lupus anticoagulant syndrome (approximate)
ICD-9-CM Siblings (same level / similar specificity) of 289.81:
289.82 - Secondary hypercoagulable state
289.83 - Myelofibrosis
289.84 - Heparin-induced thrombocytopenia (HIT)
289.89 - Other specified diseases of blood and blood-forming organs