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 .
C15.378.071.141.150.875 Thalassemia .
C15.378.071.141.150.875.100 alpha-Thalassemia .
C15.378.071.141.150.875.150 beta-Thalassemia .
C15.378.420 Hemoglobinopathies .
C15.378.420.826 Thalassemia .
C15.378.420.826.100 alpha-Thalassemia .
C15.378.420.826.150 beta-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 .
C16.320.365 Hemoglobinopathies .
C16.320.365.826 Thalassemia .
C16.320.365.826.100 alpha-Thalassemia .
C16.320.365.826.150 beta-Thalassemia .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
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. .
1.00
1709700
 
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. .
0.88
531820
 
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. .
0.81
1006821