Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Antibody detection, RBC, enzyme, 1 stage technique, including anti-human globulin |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Hemorrhagic disease of the newborn due to factor II deficiency |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
von Willebrands sygdom type IIH |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Total body iron with chelatable radioiron study |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
1 |
Whole blood unit collection (procedure) |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Hereditary spherocytosis due to spectrin deficiency |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
1 |
Acquired coagulation factor deficiency |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Mild disease manifests factor VIII activity of greater than 5% of normal |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Fresh frozen plasma thawing |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Antibody identification, leukocyte antibody |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Myelophthisic anemia |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
1 |
Failed attempted abortion with afibrinogenemia (disorder) |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Blood group typing, RH genotyping, complete |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
High molecular weight kininogen deficiency |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Platelet concentrate, preparation |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Hereditary factor VIII deficiency disease |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Akut idiopatisk trombocytopenisk purpura |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
1 |
Blood group typing A>2< |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Reagent RBC, preparation A, B or O pool |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
legal abort med afibrinogenæmi |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Special blood bank procedure, explain by report |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Hereditary factor I deficiency disease |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Antibody titration, anti-human globulin technique |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Idiopatisk trombocytopenisk purpura |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
1 |
Illegal abort med afibrinogenæmi |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Transient neonatal disorder of coagulation |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Factor XI deficiency, type II |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Hereditary factor II deficiency disease |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Moderate disease manifests factor VIII activity of 2% to 5% of normal |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Familial hemophagocytic lymphohistiocytosis |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
1 |
Isotope study of blood volume |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
1 |
Acquired factor X deficiency disease |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Hereditary spherocytosis due to deficiency of protein 4.2 |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
1 |
Disseminated intravascular coagulation in newborn |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Failed attempted abortion with defibrination syndrome (disorder) |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
von Willebrands sygdom type IID |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Preparation of antibody sensitized pooled reagent red blood cells (procedure) |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Frozen blood thawing and processing |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Antibody absorption, RBC, cold with autoabsorption |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Abort med defibrineringssyndrom |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Acquired factor XI deficiency disease |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Antibody elution, ether |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Acquired factor V deficiency disease |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Antithrombin III deficiency |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Sickle cell-thalassemia disease |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
1 |
Hemolytic uremic syndrome of childhood |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
1 |
Factor VII deficiency |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Hereditary factor X deficiency disease |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Familial multiple factor deficiency syndrome, type V |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
proaccelerinmangel |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
labil faktor-mangel |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Saliva secretor studies |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Factor XI inhibitor disorder |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Antibody elution from red blood cells (procedure) |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Anti-human globulin test, indirect, titer, non-gamma |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Blood group typing Rho(D) |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Hereditary factor VII deficiency disease (disorder) |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
von Willebrand factor inhibitor disorder |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Antibody elution, alcohol |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Eczematid-like purpura of Doucas and Kapetanakis |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
erhvervet hypoprotrombinæmi |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Factor V inhibitor disorder (disorder) |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Hereditary factor IX deficiency disease |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Secondary cryofibrinogenemia |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Major crossmatch |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Antibody elution, heat |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Factor V deficiency |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Hereditary factor XII deficiency disease |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Compatibility test, crossmatch, complete standard technique, includes typing and antibody screening of RBC |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Anticoagulant overdosage |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Blood group typing |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Hereditary dysfibrinogenemia (disorder) |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Reagent RBC, freeze, liquid nitrogen |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Intrauterine transfusion |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
1 |
Factor XI deficiency, type III |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Factor XII deficiency disease |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Factor VIII inhibitor disorder |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Packed RBC preparation |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Warfarin overdosage |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
White blood cell localization, whole body |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
1 |
Lymphocyte storage |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Antibody identification, RBC antibody panel, enzyme, 2 stage technique including anti-human globulin |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Compatibility test, crossmatch, screening for compatible unit, antiglobulin technique |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Lymphocyte storage, liquid nitrogen |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Prekallikrein deficiency |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Postpartum coagulation defect with hemorrhage |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Hereditary factor XI deficiency disease |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Blood group typing A |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Antibody titration, saline |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Hereditary factor XIII deficiency disease |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Pure red cell aplasia |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
1 |
Miscarriage with defibrination syndrome |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Microangiopathic hemolytic anemia |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
3 |
Antibody identification, RBC |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Preparation and centrifugation of packed red blood cells (procedure) |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
von Willebrands sygdom type IIE |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Hemolysin detection |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
A severe form of alpha-thalassemia that is mostly lethal, and associated with severe long-term outcome and lifelong transfusions in survivors. It is characterized by fetal onset of generalized edema, pleural and pericardial effusions, and severe hypochromic anemia. Caused by deletion or inactivation of all four alpha-globin alleles leading to a severe deficiency in alpha-globin chains of Hb, and to the production of gamma-4 tetramers (Hb Bart's) during fetal life, and beta-4 tetramers (HbH) postnatally. Hb Bart's and HbH have increased oxygen affinity resulting in ineffective tissue oxygen delivery. The disease is mostly the result of combined, biallelic deletions in the HBA1 and HBA2 genes (16p13.3). The pattern of inheritance is autosomal recessive. |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
1 |
Antibody identification, RBC, albumin and AHG |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Leukocyte poor blood preparation |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Senile purpura (disorder) |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|