Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
von Willebrand disease, type IIH |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
hémoglobinose E (trouble) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Hereditary nonspherocytic hemolytic anemia due to gamma glutamyl cysteine synthetase deficiency (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
X chromosome-linked pyridoxine responsive sideroblastic anemia |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Acquired coagulation factor deficiency |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Mild hereditary factor VIII deficiency disease (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Failed attempted termination of pregnancy with afibrinogenaemia |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
High molecular weight kininogen deficiency |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Hereditary factor VIII deficiency disease (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Immune thrombocytopenia |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Thrombocytopenia due to extracorporeal circulation (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Legal termination of pregnancy with afibrinogenemia |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Severe combined immunodeficiency disease |
localisation d'une constatation (attribut) |
True |
structure d'un système corporel |
Inferred relationship |
Some |
2 |
Hereditary factor I deficiency disease |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Illegal termination of pregnancy with afibrinogenemia |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Transient neonatal disorder of coagulation |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Factor XI deficiency, type II |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Post infectious thrombocytopenic purpura |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Hereditary factor II deficiency disease |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Moderate hereditary factor VIII deficiency disease (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Acquired factor X deficiency disease |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Hereditary nonspherocytic hemolytic anemia due to pyrimidine-5'-nucleotidase deficiency (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Severe combined immunodeficiency due to absent peripheral T cell maturation (disorder) |
localisation d'une constatation (attribut) |
True |
structure d'un système corporel |
Inferred relationship |
Some |
1 |
Thrombocytopenia caused by hypothermia (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Disseminated intravascular coagulation in newborn |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Failed attempted termination of pregnancy with defibrination syndrome |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
von Willebrand disease, type IID |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Abortion with defibrination syndrome |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Acquired factor XI deficiency disease |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Acquired factor V deficiency disease |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Antithrombin III deficiency |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Severe combined immunodeficiency due to absent adenosine deaminase (disorder) |
localisation d'une constatation (attribut) |
True |
structure d'un système corporel |
Inferred relationship |
Some |
1 |
Factor VII deficiency |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Hereditary factor X deficiency disease |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Sex-linked thrombocytopenia |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Familial multiple factor deficiency syndrome, type V |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Proaccelerin deficiency |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Labile factor deficiency |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Placement of choledochal stent |
Procedure site - Indirect (attribute) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
1 |
Factor XI inhibitor disorder |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
anémie hémolytique héréditaire |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Hereditary factor VII deficiency disease (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
von Willebrand factor inhibitor disorder |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
HNSHA due to phosphofructokinase deficiency |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Acquired hypoprothrombinemia (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Factor V inhibitor disorder |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Hereditary factor IX deficiency disease (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Secondary cryofibrinogenaemia |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Factor V deficiency (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Hereditary factor XII deficiency disease |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
surdosage en anticoagulant |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Adenosine deaminase deficiency |
localisation d'une constatation (attribut) |
True |
structure d'un système corporel |
Inferred relationship |
Some |
2 |
Hereditary dysfibrinogenemia (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Severe combined immunodeficiency due to absent interleukin-2 production (disorder) |
localisation d'une constatation (attribut) |
True |
structure d'un système corporel |
Inferred relationship |
Some |
1 |
Factor XI deficiency, type III |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Haemoglobin E trait |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Factor XII deficiency disease |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
trouble d'inhibition du facteur VIII |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Warfarin overdosage (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Cyclic thrombocytopenia (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Prekallikrein deficiency (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Postpartum coagulation defect with haemorrhage |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Severe combined immunodeficiency due to absent T cell receptor (disorder) |
localisation d'une constatation (attribut) |
True |
structure d'un système corporel |
Inferred relationship |
Some |
1 |
Hereditary factor XI deficiency disease (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Thrombocytopenia due to blood loss (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Hereditary factor XIII deficiency disease (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
hémoglobinose C (trouble) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Dilutional thrombocytopenia (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
von Willebrand disease, type IIE (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Hereditary nonspherocytic hemolytic anemia due to glutathione reductase deficiency (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Hereditary nonspherocytic hemolytic anemia due to glucose phosphate isomerase deficiency (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Hereditary nonspherocytic hemolytic anemia due to increased adenosine deaminase activity (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Nezelof's syndrome (disorder) |
localisation d'une constatation (attribut) |
True |
structure d'un système corporel |
Inferred relationship |
Some |
2 |
Factor I inhibitor disorder (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Acquired pancytopenia |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
HNSHA due to phosphoglycerate kinase deficiency |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Hereditary elliptocytosis due to deficiency of protein 4.1 |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Abscess of external nose |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
2 |
Mediterranean macrothrombocytopenia |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Familial multiple factor deficiency syndrome, type VI |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Neonatal thrombocytopenia due to idiopathic maternal thrombocytopenia |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Thalassemia-hemoglobin C disease |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Primary cryofibrinogenemia |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Illegal termination of pregnancy with defibrination syndrome |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
HNSHA due to diphosphoglycerate mutase deficiency |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Hereditary sideroblastic anemia |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Defibrination syndrome following molar AND/OR ectopic pregnancy |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Thrombocytopenia due to hypersplenism |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Acquired factor XIII deficiency disease |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Familial multiple factor deficiency syndrome, type III |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Acquired coagulation factor inhibitor disorder |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Blood coagulation disorder |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Familial multiple factor deficiency syndrome, type II |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Hereditary elliptocytosis due to beta spectrin-ankyrin interaction |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Thrombocytosis |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Legal termination of pregnancy with defibrination syndrome |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Hemoglobin D disease |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
Familial multiple factor deficiency syndrome, type IV |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|