286.9 - Other And Unspecified Coagulation Defects
The ICD 9 Code for Other and unspecified coagulation defects is listed as 286.9.
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: | 286.9 |
| Long Description: | Other and unspecified coagulation defects |
| Short Description: | Coagulat defect NEC/NOS |
| Chapter: | Diseases Of The Blood And Blood-Forming Organs |
| Block: | Coagulation defects (286-286) |
| Related Descriptions: |
Acquired coagulation disorder
Acquired coagulation factor deficiency Acquired combined coagulation factor deficiency Acquired factor X deficiency disease Acquired fibrinogen abnormality Acquired inhibitor of coagulation Alpha-2-antiplasmin deficiency Anti-factor II disorder Anticoagulant excess without bleeding Anticoagulant-induced bleeding Antithrombin III deficiency Bite of unidentified snake with coagulopathy Bleeds easily Bleeds profusely Blood coagulation disorder Blood coagulation disorder with impaired clot retraction time Blood coagulation disorder with prolonged bleeding time Blood coagulation disorder with prolonged coagulation time Blood coagulation disorder with shortened bleeding time Blood coagulation disorder with shortened coagulation time Blood does not clot properly Coagulation factor deficiency syndrome Combined coagulation factor deficiency Cryofibrinogenemia Deficiency of naturally occurring coagulation factor inhibitor Deficiency of thrombin Dermite ocre of Favre Factor V inhibitor disorder Factor X inhibitor disorder Familial multiple factor deficiency syndrome Familial multiple factor deficiency syndrome, type I Familial multiple factor deficiency syndrome, type II Familial multiple factor deficiency syndrome, type III Familial multiple factor deficiency syndrome, type IV Familial multiple factor deficiency syndrome, type V Familial multiple factor deficiency syndrome, type VI Fibrinogen in blood above reference range Hereditary coagulation factor deficiency Hereditary combined coagulation factor deficiency Hereditary elevated factor VIII Hereditary elevated factor XI Hereditary hyperfibrinogenemia Hereditary thrombophilic dysfibrinogenemia Heterozygous Factor V Leiden mutation High molecular weight kininogen deficiency Homozygous Factor V Leiden mutation Ineffective thrombopoiesis Prekallikrein deficiency Premature separation of placenta with coagulation defect Primary cryofibrinogenemia Pseudo von Willebrand disease Reactive thrombocytosis Systemic lupus erythematosus-associated antiphospholipid syndrome Thrombophilia |
| ICD-10-CM Diagnosis Codes General Equivalence Mappings (GEMS): | |
| ICD-10-CM Code: | D68.8 - Other specified coagulation defects (approximate) |
| ICD-10-CM Code: | D68.9 - Coagulation defect, unspecified (approximate) |
| ICD-9-CM Siblings (same level / similar specificity) of 286.9: | |
| 286.0 - Congenital factor VIII disorder | |
| 286.1 - Congenital factor IX disorder | |
| 286.2 - Congenital factor XI deficiency | |
| 286.3 - Congenital deficiency of other clotting factors | |
| 286.4 - Von Willebrand's disease | |
| 286.6 - Defibrination syndrome | |
| 286.7 - Acquired coagulation factor deficiency | |