serw-MX  [xml]  

 DeCS Categories

C15 Hemic and Lymphatic Diseases .
C15.378 Hematologic Diseases .
C15.378.071 Anemia .
C15.378.071.141 Anemia, Hemolytic .
C15.378.071.141.150 Anemia, Hemolytic, Congenital .
C15.378. Thalassemia .
C15.378. alpha-Thalassemia .
C15.378. beta-Thalassemia .
C15.378. delta-Thalassemia .
C15.378.420 Hemoglobinopathies .
C15.378.420.826 Thalassemia .
C15.378.420.826.100 alpha-Thalassemia .
C15.378.420.826.150 beta-Thalassemia .
C15.378.420.826.200 delta-Thalassemia .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.070 Anemia, Hemolytic, Congenital .
C16.320.070.875 Thalassemia .
C16.320.070.875.100 alpha-Thalassemia .
C16.320.070.875.150 beta-Thalassemia .
C16.320.070.875.575 delta-Thalassemia .
C16.320.365 Hemoglobinopathies .
C16.320.365.826 Thalassemia .
C16.320.365.826.100 alpha-Thalassemia .
C16.320.365.826.150 beta-Thalassemia .
C16.320.365.826.575 delta-Thalassemia .
SP8 Disasters .
SP8.473 Risk 17142 .
SP8.473.654 Hazards .
SP8.473.654.482 Geography .
SP8.473.654.482.092 Delta .
 Synonyms & Historicals
delta-Thalassemia .
delta Thalassemia .
delta-Thalassemias .
A hereditary disorder characterized by reduced or absent DELTA-GLOBIN thus effecting the level of HEMOGLOBIN A2, a minor component of adult hemoglobin monitored in the diagnosis of BETA-THALASSEMIA. .
Thalassemia .
Thalassemias .
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. .
alpha-Thalassemia .
A-Thalassemia .
Alpha Thalassemia .
Disease, Hemoglobin H .
Thalassemia alpha .
Thalassemia, Alpha .
alpha-Thalassemias .
Hemoglobin H Disease .
Thalassemia-alpha .
A disorder characterized by reduced synthesis of the alpha chains of hemoglobin. The severity of this condition can vary from mild anemia to death, depending on the number of genes deleted. .
Delta .
River Mouth .
Triangular configuration of a section of coast open to the sea, created by the alluvial deposits at the mouth of a river, often, but not always, traversed by its branches. Example: the Nile delta. (Material V - Gunn, S.W.A. Multilingual Dictionary of Disaster Medicine and International Relief, 1990) .
beta-Thalassemia .
Erythroblastic Anemia .
Mediterranean Anemia .
Microcytemia, beta Type .
Thalassemia Intermedia .
Thalassemia Major (beta-Thalassemia Major) .
Thalassemia Minor (beta-Thalassemia Minor) .
Thalassemia, beta Type .
beta Thalassemia .
Anemia, Cooley .
Anemia, Cooleys .
Anemias, Erythroblastic .
Anemias, Mediterranean .
Cooley's Anemia .
Disease, Hemoglobin F .
Intermedia, Thalassemia .
Intermedias, Thalassemia .
Major, Thalassemia (beta-Thalassemia Major) .
Majors, Thalassemia (beta-Thalassemia Major) .
Mediterranean Anemias .
Microcytemias, beta Type .
Minor, Thalassemia (beta-Thalassemia Minor) .
Minors, Thalassemia (beta-Thalassemia Minor) .
Thalassemia Intermedias .
Thalassemia Major (beta Thalassemia Major) .
Thalassemia Majors (beta-Thalassemia Major) .
Thalassemia Minor (beta Thalassemia Minor) .
Thalassemia Minors (beta-Thalassemia Minor) .
Thalassemia, beta .
Thalassemias, beta .
Thalassemias, beta Type .
Type Microcytemia, beta .
Type Microcytemias, beta .
Type Thalassemia, beta .
Type Thalassemias, beta .
beta Thalassemias .
beta Type Microcytemia .
beta Type Microcytemias .
beta Type Thalassemia .
beta Type Thalassemias .
Anemia, Cooley's .
Anemia, Erythroblastic .
Anemia, Mediterranean .
Hemoglobin F Disease .
Thalassemia Major .
Thalassemia Minor .
A disorder characterized by reduced synthesis of the beta chains of hemoglobin. There is retardation of hemoglobin A synthesis in the heterozygous form (thalassemia minor), which is asymptomatic, while in the homozygous form (thalassemia major, Cooley's anemia, Mediterranean anemia, erythroblastic anemia), which can result in severe complications and even death, hemoglobin A synthesis is absent. .