Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Red blood cell destruction finding |
Interprets |
True |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
1 |
Intravascular hemolysis |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Increased erythrocyte destruction |
Interprets |
True |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
1 |
Extravascular hemolysis |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Decreased erythrocyte destruction |
Interprets |
True |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
1 |
Hemoglobinuria |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Abnormal erythrocyte destruction |
Interprets |
True |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
1 |
Hemolysis |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hemolysis |
Is a |
True |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Mechanical hemolysis due to cardiovascular prosthetic patch |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Miscarriage with intravascular hemolysis |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Illegal abortion with intravascular hemolysis |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Legal abortion with intravascular hemolysis |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Induced termination of pregnancy complicated by intravascular hemolysis |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Kernicterus due to isoimmunization |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Traumatic cardiac hemolytic anemia |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Warm autoimmune hemolytic anemia |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Acquired hemolytic anemia |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hemolytic anemia due to nonlymphoid neoplasm |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hereditary nonspherocytic hemolytic anemia due to increased adenosine deaminase activity |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Autoimmune hemolytic anemia caused by immunoglobulin G |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Idiopathic chronic cold agglutinin disease |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Severe hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Autoimmune hemolytic anemia caused by complement |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Coombs negative hemolytic anemia |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Drug-induced enzyme deficiency anemia |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hydrops fetalis due to isoimmunization |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Drug-induced immune hemolytic anemia, immune complex type |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Chronic idiopathic autoimmune hemolytic anemia |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Glucose-6-phosphate dehydrogenase deficiency class I variant anemia |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hemolytic anemia caused by babesiosis |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Glucose-6-phosphate dehydrogenase deficiency class III variant anemia |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Mild hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hereditary nonspherocytic hemolytic anemia due to gamma glutamyl cysteine synthetase deficiency |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hereditary spherocytosis due to spectrin deficiency |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hemolytic anemia caused by Clostridium welchii |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Anemia due to pentose phosphate pathway defect |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Mild hereditary spherocytosis due to spectrin deficiency |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hemolytic disease of fetus OR newborn due to ABO immunization |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Autoimmune hemolytic anemia caused by immunoglobulin A plus complement |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hereditary spherocytosis due to deficiency of protein 4.2 |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hereditary nonspherocytic hemolytic anemia due to pyrimidine-5'-nucleotidase deficiency |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Anemia due to mechanical damage |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Glucose-6-phosphate dehydrogenase deficiency class II variant anemia |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Post-viral paroxysmal cold hemoglobinuria |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hemolytic uremic syndrome of childhood |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Immediate hemolytic transfusion reaction |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hemolytic anemia due to infection |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hereditary hemolytic anemia |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hemolytic transfusion reaction |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Polyagglutinable erythrocyte syndrome |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hereditary nonspherocytic hemolytic anemia due to phosphofructokinase deficiency |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hapten type low affinity hemolytic anemia |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Anemia due to abnormality extrinsic to the red cell |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Failed attempted abortion with intravascular hemolysis |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Secondary paroxysmal cold hemoglobinuria |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Microangiopathic hemolytic anemia |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hereditary nonspherocytic hemolytic anemia due to glutathione reductase deficiency |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hereditary nonspherocytic hemolytic anemia due to glucose phosphate isomerase deficiency |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hereditary spherocytosis |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hereditary nonspherocytic hemolytic anemia due to phosphoglycerate kinase deficiency |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hemolytic anemia with emphysema AND cutis laxa |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hemolytic anemia |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hereditary nonspherocytic hemolytic anemia due to diphosphoglycerate mutase deficiency |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Glucose-6-phosphate dehydrogenase deficiency anemia |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Autoimmune hemolytic anemia caused by immunoglobulin G plus complement |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Idiopathic paroxysmal cold hemoglobinuria |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Antibody-mediated anemia |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Late anemia due to isoimmunization |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hereditary spherocytosis due to beta spectrin defect |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Autoimmune hemolytic anemia caused by immunoglobulin M |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hereditary nonspherocytic hemolytic anemia due to pyruvate kinase deficiency |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Coombs positive hemolytic anemia |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Evans syndrome |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hemolytic anemia caused by Bartonella |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Severe hereditary spherocytosis due to spectrin deficiency |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hemolytic anemia caused by malaria |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Thrombotic thrombocytopenic purpura |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hemolytic uremic syndrome, adult type |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hereditary nonspherocytic hemolytic anemia due to decreased adenosine deaminase activity |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Glucose-6-phosphate dehydrogenase deficiency class V variant anemia |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hemolytic anemia caused by drugs |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Glucose-6-phosphate dehydrogenase deficiency class IV variant anemia |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Delayed hemolytic transfusion reaction |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hapten type high affinity hemolytic anemia |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Glucose-6-phosphate dehydrogenase variant enzyme deficiency anemia |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hemolytic disease of fetus OR newborn due to RhD isoimmunization |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Autoimmune hemolytic anemia caused by immunoglobulin A |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hemolytic uremic syndrome |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hemolytic disease of the newborn due to non-ABO, non-Rh isoimmunization |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Anemia due to enzyme deficiency |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Hereditary nonspherocytic hemolytic anemia due to glutathione synthetase deficiency |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Primary (idiopathic) autoimmune hemolytic anemia |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Secondary autoimmune hemolytic anemia |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Secondary warm autoimmune hemolytic anemia |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|
Post-infectious cold agglutinin disease |
Interprets |
False |
Erythrocyte destruction, function |
Inferred relationship |
Existential restriction modifier |
|