Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Anemia due to blood loss |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
|
Hypochromic microcytic anemia with iron overload |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
|
Hemolytic anemia caused by Bartonella |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
1 |
Hemolytic anemia caused by babesiosis |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
1 |
Mycoplasmal anemia |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
1 |
Hemolytic anemia due to infection |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
1 |
Anemia due to infection |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
1 |
Hemolytic anemia caused by Clostridium welchii |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
2 |
Oroya fever |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
2 |
Hemolytic anemia caused by malaria |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
1 |
Anemia following acute postoperative blood loss |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
|
Anemia co-occurrent and due to chronic kidney disease stage 3 |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
|
Anemia co-occurrent with human immunodeficiency virus infection |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
|
Anemia caused by zidovudine |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
4 |
Aplastic anemia co-occurrent with human immunodeficiency virus infection |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
|
Acquired hemolytic anemia co-occurrent with human immunodeficiency virus infection |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
|
Antibody mediated acquired pure red cell aplasia caused by erythropoiesis stimulating agent |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
|
Dehydrated hereditary stomatocytosis |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
4 |
Alpha thalassemia X-linked intellectual disability syndrome |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
|
Dominant beta-thalassemia |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
|
Familial pseudohyperkalemia |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
4 |
Beta thalassemia X-linked thrombocytopenia syndrome |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
|
Autosomal recessive sideroblastic anemia |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
|
Anemia co-occurrent and due to chronic kidney disease stage 4 |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
2 |
Anemia co-occurrent and due to chronic kidney disease stage 5 |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
2 |
Telangiectasia, erythrocytosis, monoclonal gammopathy, perinephric fluid collections and intrapulmonary shunting syndrome |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
4 |
Autoimmune hemolytic anemia mixed type |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
|
Lethal hemolytic anemia and genital anomaly syndrome |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
5 |
Congenital dyserythropoietic anemia type IV |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
4 |
Adult-onset autosomal recessive sideroblastic anemia |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
|
Cystic fibrosis with gastritis and megaloblastic anemia syndrome |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
5 |
Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
6 |
Megaloblastic anemia due to folate deficiency due to increased requirement |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
5 |
Megaloblastic anemia due to folate deficiency in pregnancy and lactation |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
5 |
Megaloblastic anemia due to folate deficiency in prematurity |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
5 |
Hemolytic disease of newborn co-occurrent and due to ABO immunization |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
|
X-linked congenital dyserythropoietic anemia with thrombocytopenia |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
4 |
Polycythemia neonatorum due to inherited disorder of erythropoietin production |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
2 |
Polycythemia neonatorum following blood transfusion |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
3 |
Overhydrated hereditary stomatocytosis |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
1 |
Pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
6 |
Familial hemolytic uremic syndrome |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
|
Southeast Asian ovalocytosis |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
1 |
Huntington disease-like 2 |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
3 |
McLeod neuroacanthocytosis syndrome |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
3 |
Nonspherocytic hemolytic anemia due to deficiency of adenosinetriphosphatase |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
4 |
Iron deficiency anemia due to blood loss |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
|
Acquired iron deficiency anemia due to decreased absorption |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
|
Secondary autoimmune hemolytic anemia co-occurrent and due to systemic lupus erythematosus |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
|
Secondary autoimmune hemolytic anemia co-occurrent and due to chronic inflammatory disease |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
|
Secondary autoimmune hemolytic anemia co-occurrent and due to lymphoproliferative disorder |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
|
Secondary autoimmune hemolytic anemia co-occurrent and due to rheumatic disorder |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
|
Secondary autoimmune hemolytic anemia co-occurrent and due to ulcerative colitis |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
|
Hereditary methemoglobinemia due to globin chain mutation |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
1 |
Thalassemia intermedia |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
3 |
Hemoglobin Bart's hydrops syndrome |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
3 |
A gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
3 |
Hemoglobin D trait |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
1 |
beta^+^ Thalassemia, normal Hb A>2<, type 2 |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
3 |
Delta beta thalassemia |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
3 |
Sickle cell trait |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
1 |
Delta thalassemia |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
3 |
Hereditary persistence of fetal hemoglobin thalassemia |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
3 |
Unstable hemoglobin disease |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
1 |
Heterozygous thalassemia |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
3 |
Double heterozygous sickling disorder |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
1 |
Epsilon gamma delta beta thalassemia |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
3 |
Hemoglobin E disease |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
1 |
Sickle cell-hemoglobin D disease |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
1 |
Homozygous beta thalassemia |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
3 |
Beta zero thalassemia deletion type |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
3 |
Hereditary persistence of fetal hemoglobin unlinked to beta-globulin gene cluster |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
3 |
Sickle cell-hemoglobin C disease |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
1 |
Alpha plus thalassemia |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
3 |
Sickle cell-thalassemia disease |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
4 |
Hereditary persistence of fetal hemoglobin A gamma beta^+^ thalassemia |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
3 |
Thalassemia |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
3 |
Hemoglobin E trait |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
1 |
Sickle cell-hemoglobin E disease |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
1 |
Thalassemia with other hemoglobinopathy |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
3 |
Beta plus thalassemia normal hemoglobin A>2< type 1 silent |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
3 |
Hemoglobin H disease |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
3 |
Hemoglobin C disease |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
1 |
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
3 |
Hereditary persistence of fetal hemoglobin, nondeletion type |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
3 |
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
3 |
Thalassemia-hemoglobin C disease |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
3 |
Delta zero thalassemia |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
3 |
Beta thalassemia |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
3 |
Alpha zero thalassemia |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
3 |
Hemoglobin D disease |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
1 |
Alpha thalassemia |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
3 |
Hb Lepore thalassemia |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
3 |
Epsilon gamma delta beta^0^ thalassemia |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
3 |
Thalassemia major |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
3 |
Hemoglobin C trait |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
1 |
Delta beta zero thalassemia |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
3 |
Beta plus thalassemia |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
3 |
Thalassemia syndrome |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
3 |
Alpha plus thalassemia non deletion type |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
3 |
Hereditary persistence of fetal hemoglobin deletion type |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Existential restriction modifier |
3 |