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NCIm Version: 201808 (Browser Version 2.9, using LexEVS 6.5.1)
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Blood Coagulation Disorders (CUI C0005779) Suggest changes to this concept
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'Blood Coagulation Disorders' By Source: NCI
Select source:   NCI  AOD   COSTAR   CSP   CST   DXP   FDA   HPO   ICD10   ICD10CM   ICD9CM   MDR   MEDLINEPLUS   MSH   MTH   MTHICD9   NDFRT   NICHD   OMIM   SNOMEDCT_US  

Synonyms
Term Source Source List Type Term Type Definition Code
Coagulation Disorder NCI PT C2902


Relationships
Relationship Relationship Definitions Rel. Attribute Relationship Attr. Definitions CUI Term Source Source List Type Term Type Definition Code
Parent isa C1518374 Non-Neoplastic Hematologic and Lymphocytic Disorder NCI PT C26324
Child inverse_isa C0272375 Antithrombin III Deficiency NCI PT C98815
Child inverse_isa C1458140 Bleeding Diathesis NCI PT C115221
Child inverse_isa C0272271 Coagulation Disorder Related to Liver Dysfunction NCI PT C101333
Child inverse_isa C0272315 Coagulation Factor Deficiency NCI PT C27215
Child inverse_isa C3641106 Congenital Bleeding Disorder NCI PT C103172
Child inverse_isa CL514278 Consumptive Coagulopathy NCI PT C131658
Child inverse_isa C0012739 Disseminated Intravascular Coagulation NCI PT C2992
Child inverse_isa C1260903 Dysfibrinogenemia NCI PT C131659
Child inverse_isa C0019061 Hemolytic Uremic Syndrome NCI PT C75545
Child inverse_isa C0272340 High Molecular Weight Kininogen Deficiency NCI PT C98946
Child inverse_isa C0919890 Hyperfibrinogenemia NCI PT C113740
Child inverse_isa CL514666 Immune-Mediated Coagulopathy NCI PT C131673
Child inverse_isa CL514322 Plasma Kallikrein Deficiency NCI PT C131648
Child inverse_isa C2750067 Plasminogen Activator Inhibitor-1 Deficiency NCI PT C133884
Child inverse_isa C0398623 Thrombophilia NCI PT C84479
Child inverse_isa C2717961 Thrombotic Microangiopathy NCI PT C62605
Child inverse_isa CL514344 Tissue Kallikrein Deficiency NCI PT C131651
Child inverse_isa C0042974 von Willebrand Disease NCI PT C68677
Other Concept_In_Subset C1880652 FDA Center For Devices and Radiological Health Terminology NCI PT C62596
Other Concept_In_Subset C1709489 FDA Patient Problem Code Hierarchy NCI PT C54450
Other Concept_In_Subset C3274563 Neonatal Research Network Terminology NCI PT C99147
Other Concept_In_Subset C3897974 Pediatric Adverse Events Terminology NCI PT C118464
Other Concept_In_Subset CL520485 Pediatric Hematology-Oncology Terminology NCI PT C132009
Other Concept_In_Subset C2983498 Pediatric Terminology NCI PT C90259
Other Disease_Has_Associated_Anatomic_Site C1512394 Hematopoietic and Lymphatic System NCI PT C41165
Other Disease_Has_Normal_Cell_Origin C1512385 Hematopoietic and Lymphoid Cell NCI PT C32725
Other Disease_Has_Normal_Tissue_Origin C1512398 Hematopoietic and Lymphoid Tissue NCI PT C41168
Other Has_NICHD_Parent C0007222 Cardiovascular Disorder NCI PT C2931
Other Has_NICHD_Parent C0018939 Hematologic and Lymphocytic Disorder NCI PT C26323
Other May_Be_Associated_Disease_Of_Disease C1292777 Aggressive NK-Cell Leukemia NCI PT C8647
Other May_Be_Associated_Disease_Of_Disease C1333947 Heavy Chain Deposition Disease NCI PT C7339
Other May_Be_Associated_Disease_Of_Disease C0238239 Light Chain Deposition Disease NCI PT C7727
Other Parent_Is_CDRH C0012739 Disseminated Intravascular Coagulation NCI PT C2992
Other Parent_Is_NICHD C0272375 Antithrombin III Deficiency NCI PT C98815
Other Parent_Is_NICHD C1458140 Bleeding Diathesis NCI PT C115221
Other Parent_Is_NICHD C0272315 Coagulation Factor Deficiency NCI PT C27215
Other Parent_Is_NICHD C3641106 Congenital Bleeding Disorder NCI PT C103172
Other Parent_Is_NICHD CL514278 Consumptive Coagulopathy NCI PT C131658
Other Parent_Is_NICHD C1260903 Dysfibrinogenemia NCI PT C131659
Other Parent_Is_NICHD C0272340 High Molecular Weight Kininogen Deficiency NCI PT C98946
Other Parent_Is_NICHD CL514666 Immune-Mediated Coagulopathy NCI PT C131673
Other Parent_Is_NICHD CL514322 Plasma Kallikrein Deficiency NCI PT C131648
Other Parent_Is_NICHD C0398623 Thrombophilia NCI PT C84479
Other Parent_Is_NICHD C2717961 Thrombotic Microangiopathy NCI PT C62605
Other Parent_Is_NICHD CL514344 Tissue Kallikrein Deficiency NCI PT C131651
Other Parent_Is_NICHD C0042974 von Willebrand Disease NCI PT C68677

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