Disease Index

genetic defect causing abnormal hemoglobin structure

human disease

form of anemia due to hemolysis

human disease

human disease

rare, autosomal recessive, inherited disorder caused by mutation of the BPGM gene. It is characterized by hemolytic anemia and splenomegaly

Haemolytic anaemia due to glutathione reductase (GSR) deficiency is characterised by nearly complete absence of GSR activity in erythrocytes

human disease

human disease

Human disease

uncommon hematologic disorder seen more often in children than in adults

human disease

human genetic disease that impairs the body's ability to make blood clots, a process needed to stop bleeding

X-linked disease that has material basis in Factor VIII deficiency, which results in the formation of fibrin deficient clots which makes coagulation much more prolonged

inherited blood coagulation disease that has material basis in Factor IX deficiency, which makes coagulation much more prolonged. The disease is inherited as an X-linked recessive trait

human disease

human disease

Group of clinically similar illnesses caused by species of hantaviruses

human disease

human disease

Human disease

development of thrombocytopenia (a low platelet count), due to the administration of various forms of heparin, an anticoagulant

human disease

Human disease

hepatic vascular disease that is characterized by obstruction of some of the small veins of the liver

Human disease

uncommon malignant liver cancer occurring in infants and children