| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Hemolysis |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Hemolysis (observable entity) |
est un(e) (attribut) |
True |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Mechanical hemolysis due to cardiovascular prosthetic patch (disorder) |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Miscarriage with intravascular hemolysis (disorder) |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Illegal termination of pregnancy with intravascular hemolysis |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Legal termination of pregnancy with intravascular hemolysis |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Induced termination of pregnancy complicated by intravascular haemolysis |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Red blood cell destruction finding |
interprète (attribut) |
True |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
1 |
| Intravascular hemolysis |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Increased erythrocyte destruction |
interprète (attribut) |
True |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
1 |
| Extravascular haemolysis |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Decreased erythrocyte destruction |
interprète (attribut) |
True |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
1 |
| Hemoglobinuria |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Abnormal erythrocyte destruction |
interprète (attribut) |
True |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
1 |
| Kernicterus due to isoimmunization |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Traumatic cardiac haemolytic anaemia |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| anémie hémolytique auto-immune chaude |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| anémie hémolytique acquise |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Haemolytic anaemia due to nonlymphoid neoplasm |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Hereditary nonspherocytic hemolytic anemia due to increased adenosine deaminase activity (disorder) |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Autoimmune hemolytic anemia due to IgG |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Idiopathic chronic cold agglutinin disease |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Severe hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| anémie hémolytique auto-immune due au complément |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Coombs negative hemolytic anemia |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Drug-induced enzyme deficiency anemia |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Hydrops fetalis due to isoimmunization |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Drug-induced immune hemolytic anemia, immune complex type |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Chronic idiopathic autoimmune hemolytic anemia |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Glucose-6-phosphate dehydrogenase deficiency class I variant anemia (disorder) |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Hemolytic anemia caused by babesiosis (disorder) |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Glucose-6-phosphate dehydrogenase deficiency class III variant anemia (disorder) |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Mild hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Hereditary nonspherocytic hemolytic anemia due to gamma glutamyl cysteine synthetase deficiency (disorder) |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Hereditary spherocytosis due to spectrin deficiency |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| anémie hémolytique à Clostridium welchii |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Anaemia due to pentose phosphate pathway defect |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Mild hereditary spherocytosis due to spectrin deficiency |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Haemolytic disease of foetus OR newborn due to ABO immunisation |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Autoimmune hemolytic anemia caused by immunoglobulin A plus complement (disorder) |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Hereditary spherocytosis due to deficiency of protein 4.2 |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Hereditary nonspherocytic hemolytic anemia due to pyrimidine-5'-nucleotidase deficiency (disorder) |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Anaemia due to mechanical damage |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Glucose-6-phosphate dehydrogenase deficiency class II variant anemia (disorder) |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Post-viral paroxysmal cold hemoglobinuria |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| syndrome urémique hémolytique de l'enfance |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Immediate haemolytic transfusion reaction |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Haemolytic anaemia due to infection |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| anémie hémolytique héréditaire |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Haemolytic transfusion reaction |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Polyagglutinable erythrocyte syndrome |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| HNSHA due to phosphofructokinase deficiency |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency (disorder) |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| anémie hémolytique de type haptène de faible affinité |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Anemia due to abnormality extrinsic to the red cell |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency (disorder) |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Failed attempted termination of pregnancy with intravascular hemolysis |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin (disorder) |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency (disorder) |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| hémoglobinurie froide paroxystique secondaire |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| anémie hémolytique microangiopathique |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Hereditary nonspherocytic hemolytic anemia due to glutathione reductase deficiency (disorder) |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Hereditary nonspherocytic hemolytic anemia due to glucose phosphate isomerase deficiency (disorder) |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| sphérocytose héréditaire |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| HNSHA due to phosphoglycerate kinase deficiency |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Hemolytic anemia with emphysema AND cutis laxa |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Hemolytic anemia |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| HNSHA due to diphosphoglycerate mutase deficiency |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Glucose-6-phosphate dehydrogenase deficiency anemia |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Autoimmune hemolytic anemia due to IgG plus complement |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Idiopathic paroxysmal cold hemoglobinuria |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Antibody-mediated anemia |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Late anemia due to isoimmunization |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Hereditary spherocytosis due to beta spectrin defect |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Autoimmune hemolytic anemia due to IgM |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Hereditary nonspherocytic hemolytic anemia due to pyruvate kinase deficiency (disorder) |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Coombs positive hemolytic anemia |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Evans syndrome |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Hemolytic anemia due to Bartonella |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Severe hereditary spherocytosis due to spectrin deficiency |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Hemolytic anemia due to malaria |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| purpura thrombopénique thrombotique (trouble) |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Hemolytic uremic syndrome, adult type |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| HNSHA due to decreased adenosine deaminase activity |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| G-6-PD class V variant anemia |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Hemolytic anemia due to drugs |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| G-6-PD class IV variant anemia |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Delayed hemolytic transfusion reaction |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Hapten type high affinity hemolytic anemia |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| G-6-PD variant enzyme deficiency anemia |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Hemolytic disease of fetus OR newborn due to RhD isoimmunization (disorder) |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Autoimmune hemolytic anemia due to IgA |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Hemolytic uremic syndrome |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Hemolytic disease of the newborn due to non-ABO, non-Rh isoimmunization |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Anemia due to enzyme deficiency |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| HNSHA due to aldolase A deficiency |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| HNSHA due to glutathione synthetase deficiency |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| Primary (idiopathic) autoimmune hemolytic anemia |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| anémie hémolytique auto-immune secondaire |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| anémie hémolytique auto-immune chaude secondaire |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
| maladie des agglutinines froides postinfectieuse |
interprète (attribut) |
False |
Erythrocyte destruction, function (observable entity) |
Inferred relationship |
Some |
|
FHIR