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 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 .
C15.378.071.141.150.150 Anemia, Sickle Cell .
C15.378.071.141.150.150.440 Hemoglobin SC Disease .
C15.378.071.141.150.490 Hemoglobin C Disease .
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 .
C15.378.420.155 Anemia, Sickle Cell .
C15.378.420.155.440 Hemoglobin SC Disease .
C15.378.420.463 Hemoglobin C Disease .
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 .
C16.320.070.150 Anemia, Sickle Cell .
C16.320.070.150.440 Hemoglobin SC Disease .
C16.320.070.490 Hemoglobin C Disease .
C16.320.070.875 Thalassemia .
C16.320.070.875.100 alpha-Thalassemia .
C16.320.070.875.150 beta-Thalassemia .
C16.320.365 Hemoglobinopathies .
C16.320.365.155 Anemia, Sickle Cell .
C16.320.365.155.440 Hemoglobin SC Disease .
C16.320.365.463 Hemoglobin C Disease .
C16.320.365.826 Thalassemia .
C16.320.365.826.100 alpha-Thalassemia .
C16.320.365.826.150 beta-Thalassemia .
D12 Amino Acids, Peptides, and Proteins .
D12.776 Proteins .
D12.776.124 Blood Proteins .
D12.776.124.400 Hemoglobins .
D12.776.124.400.303 Fetal Hemoglobin .
D12.776.422 Hemeproteins .
D12.776.422.316 Globins .
D12.776.422.316.762 Hemoglobins .
D12.776.422.316.762.320 Fetal Hemoglobin .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
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. .
1.00
1006821
 
Fetal Hemoglobin .
Hemoglobin, Fetal .
Hemoglobin F .
The major component of hemoglobin in the fetus. This HEMOGLOBIN has two alpha and two gamma polypeptide subunits in comparison to normal adult hemoglobin, which has two alpha and two beta polypeptide subunits. Fetal hemoglobin concentrations can be elevated (usually above 0.5%) in children and adults affected by LEUKEMIA and several types of ANEMIA. .
0.85
614660
 
Anemia, Sickle Cell .
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 .
Hemoglobin S Disease .
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. .
0.76
83317359
 
Hemoglobin C Disease .
Hemoglobin-C Disease .
C Disease, Hemoglobin .
C Diseases, Hemoglobin .
Hemoglobin C Diseases .
Hemoglobin-C Diseases .
A disease characterized by compensated hemolysis with a normal hemoglobin level or a mild to moderate anemia. There may be intermittent abdominal discomfort, splenomegaly, and slight jaundice. .
0.75
14446
 
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. .
0.73
531820
 
Hemoglobin SC Disease .
Disease, Hemoglobin SC .
Disease, SC .
Diseases, Hemoglobin SC .
Diseases, SC .
Hemoglobin SC Diseases .
SC Disease, Hemoglobin .
SC Diseases .
SC Diseases, Hemoglobin .
SC Disease .
Sickle Cell Hemoglobin C Disease .
One of the sickle cell disorders characterized by the presence of both hemoglobin S and hemoglobin C. It is similar to, but less severe than sickle cell anemia. .
0.71
99586