Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Leptocyte |
Is a |
True |
Erythrocyte |
Inferred relationship |
Some |
|
rhytiocyt |
Is a |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Red blood cell precursor |
Is a |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Erythroid precursor cell |
Is a |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Reticulocyte |
Is a |
True |
Erythrocyte |
Inferred relationship |
Some |
|
Siderocyte |
Is a |
True |
Erythrocyte |
Inferred relationship |
Some |
|
Megaloblastic anemia due to exfoliative dermatitis |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Red blood cell size determination (procedure) |
Has measured component |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Erythrocyte sedimentation rate |
Measures |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Red blood cell count, automated, cerebrospinal fluid |
Has measured component |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Red blood cell count, manual, peritoneal fluid |
Has measured component |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Red blood cell count, automated, pleural fluid (procedure) |
Has measured component |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Red blood cell count, automated, urine |
Has measured component |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Red blood cell count, automated, synovial fluid |
Has measured component |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Kongenit elliptocytose |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Anemia related to disturbed DNA synthesis |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Severe hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Some |
5 |
Hereditary elliptocytosis |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Some |
1 |
Favism |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Some |
1 |
Beta thalassemia intermedia |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Hereditary persistence of fetal hemoglobin |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Anemia in neoplastic disease |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Megaloblastic anemia due to poor nutrition |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Polycythemia vera (clinical) |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
refraktær anæmi |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Myelodysplastic syndrome with ring sideroblasts and single lineage dysplasia (disorder) |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Refractory anaemia with excess blasts (clinical) |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Anaemia refractoria med overskydende blaster i transformation (klinisk) |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Sickle cell-haemoglobin C retinopathy |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Chicken anemia virus infection |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Non-anaemic red cell disorder |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Some |
1 |
Iron deficiency without anemia |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Some |
1 |
Alcohol-related macrocytosis |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Some |
2 |
Dilutional anaemia |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Anaemia of chronic disease |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Anaemia of renal disease |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Microcytic anemia |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Congenital transferrin deficiency |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Selective malabsorption of cyanocobalamin |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Combined deficiency anaemia |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Thiamine-responsive macrocytosis |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Alcohol-related sideroblastic anaemia |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Transient erythroblastopenia of childhood |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Acquired red cell aplasia |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Kell isoimmunization of the newborn |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Maternal autoimmune hemolytic anemia |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Alpha thalassemia trait |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Haemoglobin Constant Spring trait |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Hemoglobin Lepore trait |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Delta-beta-Lepore thalassaemia |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Alpha-beta thalassemia |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Gamma thalassaemia |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Sickle cell anemia with high hemoglobin F |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Hemoglobin E/beta thalassemia disease |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Low affinity haemoglobin |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Some |
1 |
High affinity hemoglobin |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Some |
1 |
methæmoglobinreductasemangel |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Secondary polycythaemia without excess erythropoietin |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Some |
2 |
Erythrocyte enzyme deficiency |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Some |
1 |
Chronic non-spherocytic haemolytic anaemia |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Some |
1 |
Phosphoglycerokinase deficiency |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Some |
1 |
Glucose phosphate isomerase deficiency |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Some |
1 |
Triose phosphate isomerase deficiency |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Some |
1 |
muskelphosphofructokinasemangel |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Uridine monophosphate hydrolase deficiency |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Some |
1 |
Adenosine deaminase overproduction |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Some |
1 |
Erythrocyte membrane abnormality |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Some |
1 |
Hereditary elliptocytosis with transient poikilocytosis |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
1 |
Blood group deletion syndrome |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Some |
1 |
Abnormal cation transport syndrome |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Some |
1 |
alfa/beta-lipoproteinæmi |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
1 |
Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Pearson's syndrome |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
A rare lipoprotein metabolism disorder characterised clinically by corneal opacities and sometimes renal failure and haemolytic anaemia, and biochemically by severely reduced HDL cholesterol. Age of onset is variable but most patients are diagnosed during adulthood. Two familial forms of LCAT deficiency have been reported: familial LCAT deficiency characterised by corneal opacities, anaemia and renal insufficiency and Fish-eye disease characterised by corneal opacities and sometimes atherosclerosis. LCAT deficiency is caused by deficient or absent catalytic activity of the LCAT enzyme, which catalyses the formation of cholesterol esters in lipoproteins and is encoded by the LCAT gene (16q22.1). Accumulation of unesterified cholesterol in the body for example in the cornea, erythrocytes and kidneys, is thought to underlie the clinical manifestations. |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
1 |
A form of genetic LCAT (lecithin-cholesterol acyltransferase) deficiency characterised clinically by corneal opacifications, and biochemically by significantly reduced HDL cholesterol and partial LCAT enzyme deficiency. The disease is very rare. Corneal opacities are progressive and are observed from an early age (adolescence or young adulthood) and sometimes result in visual impairment. These lesions are generally more severe than in complete LCAT deficiency and form a mosaic pattern of small dot-like grey-white opacities. Signs of atherosclerosis have only been reported in rare cases although patients have low HDL cholesterol levels. In patients with this disorder, alpha-LCAT activity is abolished, but beta-LCAT activity is preserved. Impaired enzyme function is thought to result in deposition of lipids in the cornea. The disease follows an autosomal recessive pattern of inheritance. |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
1 |
Hemolytic uremic syndrome |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Hemolytic disease of fetus OR newborn due to isoimmunization |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Hemolytic disease of the newborn due to non-ABO, non-Rh isoimmunization |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Anemia due to infection |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Congenital atransferrinaemia |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Beta zero thalassemia non deletion type (disorder) |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
anæmi forårsaget af ukendte eller multiple mekanismer |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Anemia due to copper deficiency |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Anemia due to membrane defect |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Acquired stomatocytosis (disorder) |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Anemia due to enzyme deficiency |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
4 |
hereditær non-sfærocytisk hæmolytisk anæmi forårsaget af aldolase A-mangel |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
4 |
Hereditary nonspherocytic hemolytic anemia due to glutathione synthetase deficiency (disorder) |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Some |
4 |
March hemoglobinuria |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Anemia caused by physical agent (disorder) |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
hæmolytisk anæmi associeret med reumatisk sygdom |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Red blood cell maturation age determination |
Has measured component |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Hereditary acanthocytosis |
Finding site |
True |
Erythrocyte |
Inferred relationship |
Some |
2 |
Beta thalassaemia trait |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Anemia due to niacin deficiency |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Anemia |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Relative anemia |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
T-cell mediated cytopenia |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Idiopathic sideroblastic anemia |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Physiological anemia of infancy |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|
Late anaemia of newborn |
Finding site |
False |
Erythrocyte |
Inferred relationship |
Some |
|