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EXPERIMENTAL FACTOR ONTOLOGY - ANNOTATIONS

Term:inherited blood coagulation disorder
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Accession:EFO:MONDO:0021181 term browser browse the term
Definition:Hemorrhagic and thrombotic disorders that occur as a consequence of inherited abnormalities in blood coagulation.
Synonyms:exact_synonym: hereditary blood coagulation disease;   hereditary blood coagulation disorders;   hereditary coagulation disorder;   hereditary coagulation disorders;   inherited blood coagulation disorders;   inherited coagulation disorder;   inherited coagulation disorders;   rare genetic coagulation disorder
 related_synonym: inherited blood coagulation disease
 alt_id: MONDO:0021181
 xref: DOID:2214;   GARD:20319;   MESH:D025861;   ORDO:183654;   UMLS:C0852077


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Term paths to the root
Path 1
Term Annotations click to browse term
  experimental factor 0
    material property 0
      disposition 0
        disease 0
          genetic disorder 0
            inherited blood coagulation disorder 0
              Ehlers-Danlos syndrome, fibronectinemic type 0
              Glanzmann thrombasthenia + 0
              Hermansky-Pudlak syndrome + 0
              Scott syndrome 0
              Wiskott-Aldrich syndrome 0
              alpha-2-plasmin inhibitor deficiency 0
              autoimmune thrombocytopenic purpura 0
              congenital factor V deficiency 0
              congenital factor XI deficiency 0
              congenital factor XII deficiency 0
              congenital high-molecular-weight kininogen deficiency 0
              congenital plasminogen activator inhibitor type 1 deficiency 0
              congenital thrombotic thrombocytopenic purpura 0
              congenital vitamin K-dependent coagulation factors deficiency + 0
              cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder 0
              factor V and factor VIII, combined deficiency of, type 1 0
              factor XIII, A subunit, deficiency of 0
              familial thrombomodulin anomalies 0
              hemophilia A + 0
              hemophilia B + 0
              hereditary hemolytic uremic syndrome + 0
              hereditary thrombocytopenia and hematologic cancer predisposition syndrome + 0
              hereditary thrombocytosis with transverse limb defect 0
              hereditary von Willebrand disease + 0
              hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency 0
              hypoplasminogenemia 0
              inherited prekallikrein deficiency 0
              inherited thrombophilia + 0
              platelet-type bleeding disorder 10 0
              platelet-type bleeding disorder 14 0
              platelet-type bleeding disorder 18 0
              platelet-type bleeding disorder 8 0
Path 2
Term Annotations click to browse term
  experimental factor 0
    material property 0
      disposition 0
        disease 0
          hematologic disease 0
            blood coagulation disease 0
              inherited blood coagulation disorder 0
                Ehlers-Danlos syndrome, fibronectinemic type 0
                Glanzmann thrombasthenia + 0
                Hermansky-Pudlak syndrome + 0
                Scott syndrome 0
                Wiskott-Aldrich syndrome 0
                alpha-2-plasmin inhibitor deficiency 0
                autoimmune thrombocytopenic purpura 0
                congenital factor V deficiency 0
                congenital factor XI deficiency 0
                congenital factor XII deficiency 0
                congenital high-molecular-weight kininogen deficiency 0
                congenital plasminogen activator inhibitor type 1 deficiency 0
                congenital thrombotic thrombocytopenic purpura 0
                congenital vitamin K-dependent coagulation factors deficiency + 0
                cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder 0
                factor V and factor VIII, combined deficiency of, type 1 0
                factor XIII, A subunit, deficiency of 0
                familial thrombomodulin anomalies 0
                hemophilia A + 0
                hemophilia B + 0
                hereditary hemolytic uremic syndrome + 0
                hereditary thrombocytopenia and hematologic cancer predisposition syndrome + 0
                hereditary thrombocytosis with transverse limb defect 0
                hereditary von Willebrand disease + 0
                hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency 0
                hypoplasminogenemia 0
                inherited prekallikrein deficiency 0
                inherited thrombophilia + 0
                platelet-type bleeding disorder 10 0
                platelet-type bleeding disorder 14 0
                platelet-type bleeding disorder 18 0
                platelet-type bleeding disorder 8 0
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