Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Parvoviral aplastic crisis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
Aplastic anemia caused by antineoplastic agent |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
Aplastic anemia caused by antineoplastic agent |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
Aplastic anemia caused by antineoplastic agent |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
Aplastic anemia caused by antineoplastic agent |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
5 |
Aplastic anaemia co-occurrent with human immunodeficiency virus infection |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
Aplastic anaemia co-occurrent with human immunodeficiency virus infection |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
Aplastic anaemia co-occurrent with human immunodeficiency virus infection |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
Aplastic anaemia co-occurrent with human immunodeficiency virus infection |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
Aplastic anemia due to infection |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
5 |
Aplastic anemia due to infection |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
Aplastic anemia due to infection |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
Aplastic anemia due to radiation |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
5 |
Aplastic anemia due to radiation |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
Aplastic anaemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
Aplastic anaemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
Aplastic anaemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
5 |
Aplastic anaemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
Estren-Dameshek anemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
Antibody mediated acquired pure red cell aplasia caused by erythropoiesis stimulating agent (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
Antibody mediated acquired pure red cell aplasia caused by erythropoiesis stimulating agent (disorder) |
Has interpretation |
False |
Below reference range |
Inferred relationship |
Some |
5 |
Antibody mediated acquired pure red cell aplasia caused by erythropoiesis stimulating agent (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
Antibody mediated acquired pure red cell aplasia caused by erythropoiesis stimulating agent (disorder) |
Has interpretation |
False |
Below reference range |
Inferred relationship |
Some |
2 |
Thrombocytopenia with congenital dyserythropoietic anemia is a rare hematological disorder, seen almost exclusively in males, characterized by moderate to severe thrombocytopenia with hemorrhages with or without the presence of mild to severe anemia. |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
Thrombocytopenia with congenital dyserythropoietic anemia is a rare hematological disorder, seen almost exclusively in males, characterized by moderate to severe thrombocytopenia with hemorrhages with or without the presence of mild to severe anemia. |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
Transient hypoplastic anaemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
Transient hypoplastic anaemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
Aplastic anemia with AIDS (acquired immunodeficiency syndrome) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
Aplastic anemia with AIDS (acquired immunodeficiency syndrome) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
5 |
Aplastic anemia with AIDS (acquired immunodeficiency syndrome) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
Aplastic anemia with AIDS (acquired immunodeficiency syndrome) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
Transient erythroblastopenia of childhood |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
Anaemia co-occurrent with human immunodeficiency virus infection |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
Anaemia co-occurrent with human immunodeficiency virus infection |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
GATA binding protein 1 related thrombocytopenia with dyserythropoiesis (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
GATA binding protein 1 related thrombocytopenia with dyserythropoiesis (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
Chronic acquired pure red cell aplasia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
Chronic acquired pure red cell aplasia |
Has interpretation |
False |
Below reference range |
Inferred relationship |
Some |
5 |
Chronic acquired pure red cell aplasia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
Chronic acquired pure red cell aplasia |
Has interpretation |
False |
Below reference range |
Inferred relationship |
Some |
4 |
Congenital dyserythropoietic anemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
Congenital dyserythropoietic anemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
Congenital dyserythropoietic anemia, type I |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
Congenital dyserythropoietic anemia, type I |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
Constitutional aplastic anemia with malformation |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
Constitutional aplastic anemia with malformation |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
Constitutional aplastic anemia with malformation |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
5 |
Constitutional red cell aplasia and hypoplasia |
Has interpretation |
False |
Below reference range |
Inferred relationship |
Some |
1 |
Aplastic anaemia due to chronic disease |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
Aplastic anaemia due to chronic disease |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
Aplastic anaemia due to chronic disease |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
Aplastic anaemia due to chronic disease |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
5 |
Anemia co-occurrent and due to chronic kidney disease stage 5 (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
Anemia co-occurrent and due to chronic kidney disease stage 5 (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
Aplastic anemia due to drugs |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
Aplastic anemia due to drugs |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
Aplastic anemia due to drugs |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
Aplastic anemia due to drugs |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
5 |
Congenital dyserythropoietic anemia, type III |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
Congenital dyserythropoietic anemia, type III |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
Constitutional aplastic anemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
Constitutional aplastic anemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
Constitutional aplastic anemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
Constitutional aplastic anemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
5 |
A rare constitutional aplastic anemia disorder characterized by severe hypo/aplastic anemia or pancytopenia associated with skeletal anomalies (such as radial/ulnar defects and hand/digit abnormalities) and an increased risk of leukemia. There have been no further descriptions in the literature since 1995. |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
A rare constitutional aplastic anemia disorder characterized by severe hypo/aplastic anemia or pancytopenia associated with skeletal anomalies (such as radial/ulnar defects and hand/digit abnormalities) and an increased risk of leukemia. There have been no further descriptions in the literature since 1995. |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
5 |
A rare constitutional aplastic anemia disorder characterized by severe hypo/aplastic anemia or pancytopenia associated with skeletal anomalies (such as radial/ulnar defects and hand/digit abnormalities) and an increased risk of leukemia. There have been no further descriptions in the literature since 1995. |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
A rare constitutional aplastic anemia disorder characterized by severe hypo/aplastic anemia or pancytopenia associated with skeletal anomalies (such as radial/ulnar defects and hand/digit abnormalities) and an increased risk of leukemia. There have been no further descriptions in the literature since 1995. |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
Humoral immunologic aplastic anemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
Humoral immunologic aplastic anemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
Humoral immunologic aplastic anemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
5 |
Humoral immunologic aplastic anemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
Hemolytic uremic syndrome of childhood |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
Aplastic anemia associated with pancreatitis (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
Aplastic anemia associated with pancreatitis (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
Aplastic anemia associated with pancreatitis (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
Aplastic anemia associated with pancreatitis (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
5 |
Diarrhea-associated hemolytic uremic syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
Congenital hemolytic uremic syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
Aplastic anemia caused by toxic cause |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
5 |
Aplastic anemia caused by toxic cause |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
Acquired aplastic anemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
5 |
Acquired aplastic anemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
Acquired aplastic anemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
Acquired aplastic anemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
Aplastic anemia associated with pregnancy (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
Aplastic anemia associated with pregnancy (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
5 |
Idiopathic aplastic anaemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
Idiopathic aplastic anaemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
5 |
Idiopathic aplastic anaemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
Idiopathic aplastic anaemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
Congenital anemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
Congenital anemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
A rare acquired aplastic anaemia characterised by a severe normocytic anaemia with normal peripheral leukocyte and platelet counts, reticulocytopenia, high serum ferritin and transferrin saturation levels and isolated, almost complete absence of erythroblasts in the bone marrow with normal granulopoiesis and megakaryopoiesis. It presents with signs of severe anaemia (fatigue, lethargy, pallor, intolerance of physical exercise and exertional dyspnoea) in the absence of haemorrhagic symptoms. |
Has interpretation |
False |
Below reference range |
Inferred relationship |
Some |
5 |
A rare acquired aplastic anaemia characterised by a severe normocytic anaemia with normal peripheral leukocyte and platelet counts, reticulocytopenia, high serum ferritin and transferrin saturation levels and isolated, almost complete absence of erythroblasts in the bone marrow with normal granulopoiesis and megakaryopoiesis. It presents with signs of severe anaemia (fatigue, lethargy, pallor, intolerance of physical exercise and exertional dyspnoea) in the absence of haemorrhagic symptoms. |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
A rare acquired aplastic anaemia characterised by a severe normocytic anaemia with normal peripheral leukocyte and platelet counts, reticulocytopenia, high serum ferritin and transferrin saturation levels and isolated, almost complete absence of erythroblasts in the bone marrow with normal granulopoiesis and megakaryopoiesis. It presents with signs of severe anaemia (fatigue, lethargy, pallor, intolerance of physical exercise and exertional dyspnoea) in the absence of haemorrhagic symptoms. |
Has interpretation |
False |
Below reference range |
Inferred relationship |
Some |
4 |
A rare acquired aplastic anaemia characterised by a severe normocytic anaemia with normal peripheral leukocyte and platelet counts, reticulocytopenia, high serum ferritin and transferrin saturation levels and isolated, almost complete absence of erythroblasts in the bone marrow with normal granulopoiesis and megakaryopoiesis. It presents with signs of severe anaemia (fatigue, lethargy, pallor, intolerance of physical exercise and exertional dyspnoea) in the absence of haemorrhagic symptoms. |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
Pure red cell aplasia, acquired |
Has interpretation |
False |
Below reference range |
Inferred relationship |
Some |
4 |
Pure red cell aplasia, acquired |
Has interpretation |
False |
Below reference range |
Inferred relationship |
Some |
5 |