BIOMAT Database Logo BIOMAT Database Logo

ABC of clinical haematology. The hereditary anaemias. 1997

D J Weatherall
Institute of Molecular Medicine, University of Oxford, John Radcliffe Hospital.

UI MeSH Term Description Entries
D005955 Glucosephosphate Dehydrogenase Deficiency A disease-producing enzyme deficiency subject to many variants, some of which cause a deficiency of GLUCOSE-6-PHOSPHATE DEHYDROGENASE activity in erythrocytes, leading to hemolytic anemia. Deficiency of Glucose-6-Phosphate Dehydrogenase,Deficiency, GPD,Deficiency, Glucosephosphate Dehydrogenase,G6PD Deficiency,GPD Deficiency,Glucose 6 Phosphate Dehydrogenase Deficiency,Glucose-6-Phosphate Dehydrogenase Deficiency,Glucosephosphate Dehydrogenase Deficiencies,Hemolytic Anemia Due to G6PD Deficiency,Deficiencies, G6PD,Deficiencies, GPD,Deficiencies, Glucose-6-Phosphate Dehydrogenase,Deficiencies, Glucosephosphate Dehydrogenase,Deficiency of Glucose 6 Phosphate Dehydrogenase,Deficiency, G6PD,Deficiency, Glucose-6-Phosphate Dehydrogenase,Dehydrogenase Deficiencies, Glucose-6-Phosphate,Dehydrogenase Deficiencies, Glucosephosphate,Dehydrogenase Deficiency, Glucose-6-Phosphate,Dehydrogenase Deficiency, Glucosephosphate,G6PD Deficiencies,GPD Deficiencies,Glucose-6-Phosphate Dehydrogenase Deficiencies
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000740 Anemia A reduction in the number of circulating ERYTHROCYTES or in the quantity of HEMOGLOBIN. Anemias
D000755 Anemia, Sickle Cell A disease characterized by chronic hemolytic anemia, episodic painful crises, and pathologic involvement of many organs. It is the clinical expression of homozygosity for hemoglobin S. Hemoglobin S Disease,HbS Disease,Sickle Cell Anemia,Sickle Cell Disease,Sickle Cell Disorders,Sickling Disorder Due to Hemoglobin S,Anemias, Sickle Cell,Cell Disease, Sickle,Cell Diseases, Sickle,Cell Disorder, Sickle,Cell Disorders, Sickle,Disease, Hemoglobin S,Hemoglobin S Diseases,Sickle Cell Anemias,Sickle Cell Diseases,Sickle Cell Disorder
D013789 Thalassemia A group of hereditary hemolytic anemias in which there is decreased synthesis of one or more hemoglobin polypeptide chains. There are several genetic types with clinical pictures ranging from barely detectable hematologic abnormality to severe and fatal anemia. Thalassemias

Related Publications

D J Weatherall
ABC of clinical haematology. Macrocytic anaemias.
February 1997, BMJ (Clinical research ed.),
D J Weatherall
ABC of clinical haematology. The myelodysplastic syndromes.
March 1997, BMJ (Clinical research ed.),
D J Weatherall
ABC of clinical haematology. The acute leukaemias.
March 1997, BMJ (Clinical research ed.),
D J Weatherall
ABC of clinical haematology. Haematological emergencies.
May 1997, BMJ (Clinical research ed.),
D J Weatherall
ABC of clinical haematology. Platelet disorders.
March 1997, BMJ (Clinical research ed.),
D J Weatherall
[Hereditary anaemias].
October 2021, Ugeskrift for laeger,
D J Weatherall
ABC of clinical haematology. Iron deficiency anaemia.
February 1997, BMJ (Clinical research ed.),
D J Weatherall
ABC of clinical haematology. Chronic myeloid leukaemia.
March 1997, BMJ (Clinical research ed.),
D J Weatherall
ABC of clinical haematology. The future of haematology, molecular biology, and gene therapy.
May 1997, BMJ (Clinical research ed.),
D J Weatherall
The hereditary haemolytic anaemias.
April 1974, Journal of the Royal College of Physicians of London,
Copied contents to your clipboard!