Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Pericarditis associated with severe chronic anemia |
Interprets |
False |
Red blood cell count |
Inferred relationship |
Some |
3 |
Anaemia due to metabolic disorder |
Interprets |
False |
Red blood cell count |
Inferred relationship |
Some |
4 |
Red blood cell count, automated, cerebrospinal fluid |
Is a |
True |
Red blood cell count |
Inferred relationship |
Some |
|
Red blood cell count, manual, peritoneal fluid |
Is a |
True |
Red blood cell count |
Inferred relationship |
Some |
|
Red blood cell count, automated, pleural fluid |
Is a |
True |
Red blood cell count |
Inferred relationship |
Some |
|
Red blood cell count, automated, urine (procedure) |
Is a |
True |
Red blood cell count |
Inferred relationship |
Some |
|
A constitutional microcytic, hypochromic anemia of varying severity that is clinically characterized by manifestations of anemia and iron overload and that may respond to treatment with pyridoxine and folic acid. |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
2 |
Congenital hemolytic anemia |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
3 |
A form of constitutional sideroblastic anemia characterized by severe microcytic anemia, B-cell lymphopenia, panhypogammaglobulinemia and variable neurodegeneration. The disease presents in infancy with recurrent febrile illnesses, gastrointestinal disturbances, developmental delay, seizures, ataxia and sensorineural deafness. |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Hemolytic anemia due to adenylate kinase deficiency is a rare hemolytic anemia due to an erythrocyte nucleotide metabolism disorder characterized by moderate to severe chronic nonspherocytic hemolytic anemia that may require regular blood transfusions and/or splenectomy and may be associated with psychomotor impairment. |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
2 |
Anemia co-occurrent and due to chronic kidney disease stage 4 (disorder) |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
2 |
Congenital hypoplastic anemia |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
3 |
Pure red cell aplasia |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Acquired red cell aplasia |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Aplastic anemia caused by antineoplastic agent |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
4 |
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. |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
3 |
Transient hypoplastic anaemia |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
2 |
Transient erythroblastopenia of childhood |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Anaemia co-occurrent with human immunodeficiency virus infection |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
2 |
Chronic acquired pure red cell aplasia |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
3 |
Congenital dyserythropoietic anemia, type I |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
2 |
Constitutional red cell aplasia and hypoplasia |
Interprets |
False |
Red blood cell count |
Inferred relationship |
Some |
1 |
Anemia co-occurrent and due to chronic kidney disease stage 5 (disorder) |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
2 |
Congenital dyserythropoietic anemia, type III |
Interprets |
True |
Red blood cell count |
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. |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
5 |
Humoral immunologic aplastic anemia |
Interprets |
True |
Red blood cell count |
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. |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
3 |
Mycoplasmal anemia (disorder) |
Interprets |
False |
Red blood cell count |
Inferred relationship |
Some |
1 |
Congenital dyserythropoietic anemia type IV (CDA IV) is a newly discovered form of CDA characterized by ineffective erythropoiesis and hemolysis that leads to severe anemia at birth. |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Constitutional red cell hypoplasia |
Interprets |
False |
Red blood cell count |
Inferred relationship |
Some |
2 |
Transient acquired pure red cell aplasia |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
2 |
Cellular immunologic aplastic anemia |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
4 |
Congenital dyserythropoietic anemia, type II |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
2 |
Anemia due to infection |
Interprets |
False |
Red blood cell count |
Inferred relationship |
Some |
1 |
Acute pure red cell aplasia |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Unstable hemoglobin disease |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
2 |
GATA binding protein 1 related thrombocytopenia with dyserythropoiesis (disorder) |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Congenital dyserythropoietic anemia |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
2 |
Congenital anemia |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
2 |
Anaemia caused by zidovudine |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Antibody mediated acquired pure red cell aplasia caused by erythropoiesis stimulating agent (disorder) |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
4 |
Aplastic anemia with AIDS (acquired immunodeficiency syndrome) |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
5 |
Aplastic anaemia due to chronic disease |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
4 |
Pure red cell aplasia, acquired |
Interprets |
False |
Red blood cell count |
Inferred relationship |
Some |
4 |
Acquired aplastic anemia |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
4 |
Idiopathic aplastic anaemia |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
4 |
Aplastic anemia associated with metabolic alteration (disorder) |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
4 |
Immunologic aplastic anemia |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
4 |
Secondary aplastic anemia |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
4 |
Aplastic anemia due to drugs |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
4 |
Aplastic anemia associated with pancreatitis (disorder) |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
4 |
Constitutional aplastic anemia |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
4 |
Aplastic anaemia co-occurrent with human immunodeficiency virus infection |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Aplastic anaemia |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
3 |
Constitutional aplastic anemia with malformation |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Revesz syndrome is a rare severe phenotypic variant of dyskeratosis congenita with an onset in early childhood, characterized by features of DC (e.g. skin hyper/hypopigmentation, nail dystrophy, oral leukoplakia, high risk of bone marrow failure (BMF) and cancer, developmental delay sparse and fine hair) in conjunction with bilateral exudative retinopathy, and intracranial calcifications. |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
4 |
Parvoviral aplastic crisis |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Aplastic anemia due to infection |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
4 |
A rare genetic disease characterized by cerebellar ataxia, cytopenias and predisposition to bone marrow failure and myeloid leukemia. Neurologic features variably include slowly progressive cerebellar ataxia or balance impairment with cerebellar atrophy and periventricular white matter T2 hyperintensities in brain MRI, horizontal and vertical nystagmus, dysmetria, dysarthria, pyramidal tract signs and reduced nerve conduction velocity. Hematological abnormalities are variable and may be intermittent and include cytopenias of all cell lineages, immunodeficiency, myelodysplasia and acute myeloid leukemia. |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
4 |
Erythrocytosis caused by low atmospheric pressure |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Erythrocytosis due to cerebellar hemangioma |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Secondary polycythemia with excess erythropoietin |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Erythrocytosis due to cardiovascular disease |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
High oxygen affinity haemoglobin polycythaemia |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Erythrocytosis due to defective oxygen transport |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Erythrocytosis |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Polycythemia due to maternal-fetal transfusion |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Relative polycythemia (disorder) |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Erythrocytosis due to cyanotic congenital heart disease |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Erythrocytosis due to pulmonary disease |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Pseudo-polycythemia (disorder) |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Erythrocytosis due to renal tumor |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Polycythemia neonatorum due to inherited disorder of erythropoietin production (disorder) |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Familial erythrocytosis due to diphosphoglycerate mutase deficiency |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Familial polycythemia vera |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
2 |
Neonatal polycythaemia due to intra-uterine growth retardation |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Gaisbock's syndrome |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Neonatal polycythemia |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Erythrocytosis due to hepatoma |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Erythrocytosis due to endocrine disorder (disorder) |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Secondary polycythaemia without excess erythropoietin |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Neonatal polycythaemia due to placental insufficiency |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Inappropriate secondary erythrocytosis |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Erythrocytosis due to polycythemia vera (disorder) |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Erythrocytosis due to renal cyst |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Stress polycythemia |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Polycythemia due to donor twin transfusion |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Idiopathic erythrocytosis |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Hemoglobinopathy with erythrocytosis |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Familial erythrocytosis |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Erythrocytosis due to autotransfusion |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Secondary polycythaemia |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Polycythaemia due to cyanotic heart disease |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Polycythaemia due to cyanotic respiratory disease |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Erythrocytosis due to alveolar hypoventilation |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Erythrocytosis due to hydronephrosis |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Erythrocytosis due to tissue hypoxemia |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Polycythemia neonatorum following blood transfusion (disorder) |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Erythrocytosis due to uterine myoma |
Interprets |
True |
Red blood cell count |
Inferred relationship |
Some |
1 |
Anemia due to and following chemotherapy |
Interprets |
False |
Red blood cell count |
Inferred relationship |
Some |
2 |