serw-MX  [xml]  
 


    
 DeCS Categories

A11 Cells .
A11.118 Blood Cells .
A11.118.290 Erythrocytes .
A11.118.290.330 Erythrocytes, Abnormal .
A11.118.290.330.315 Erythrocyte Inclusions .
A11.118.290.330.315.335 Heinz Bodies .
A11.284 Cellular Structures .
A11.284.420 Inclusion Bodies .
A11.284.420.204 Erythrocyte Inclusions .
A11.284.420.204.335 Heinz Bodies .
A15 Hemic and Immune Systems .
A15.145 Blood .
A15.145.229 Blood Cells .
A15.145.229.334 Erythrocytes .
A15.145.229.334.330 Erythrocytes, Abnormal .
A15.145.229.334.330.340 Erythrocyte Inclusions .
A15.145.229.334.330.340.335 Heinz Bodies .
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 .
C15.378.071.141.150.875.575 delta-Thalassemia .
C15.378.420 Hemoglobinopathies .
C15.378.420.826 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 .
C16.320.070.875.575 delta-Thalassemia .
C16.320.365 Hemoglobinopathies .
C16.320.365.826 Thalassemia .
C16.320.365.826.575 delta-Thalassemia .
C23 Pathological Conditions, Signs and Symptoms .
C23.888 Signs and Symptoms .
C23.888.248 Cyanosis .
D12 Amino Acids, Peptides, and Proteins .
D12.776 Proteins .
D12.776.124 Blood Proteins .
D12.776.124.400 Hemoglobins .
D12.776.124.400.405 Hemoglobin A .
D12.776.124.400.463 Hemoglobins, Abnormal .
D12.776.422 Hemeproteins .
D12.776.422.316 Globins .
D12.776.422.316.762 Hemoglobins .
D12.776.422.316.762.380 Hemoglobin A .
D12.776.422.316.762.426 Hemoglobins, Abnormal .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Heinz Bodies .
Bodies, Heinz .
Abnormal intracellular inclusions, composed of denatured hemoglobin, found on the membrane of red blood cells. They are seen in thalassemias, enzymopathies, hemoglobinopathies, and after splenectomy. .
1.00
4607
 
Hemoglobinopathies .
Hemoglobinopathy .
A group of inherited disorders characterized by structural alterations within the hemoglobin molecule. .
0.55
2823516
 
Hemoglobins .
Eryhem .
Ferrous Hemoglobin .
Hemoglobin .
Hemoglobin, Ferrous .
The oxygen-carrying proteins of ERYTHROCYTES. They are found in all vertebrates and some invertebrates. The number of globin subunits in the hemoglobin quaternary structure differs between species. Structures range from monomeric to a variety of multimeric arrangements. .
0.47
76958519
 
Hemoglobins, Abnormal .
Abnormal Hemoglobins .
Hemoglobins characterized by structural alterations within the molecule. The alteration can be either absence, addition or substitution of one or more amino acids in the globin part of the molecule at selected positions in the polypeptide chains. .
0.47
716504
 
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. .
0.44
037
 
Hemoglobin A .
Normal adult human hemoglobin. The globin moiety consists of two alpha and two beta chains. .
0.43
623144
 
Cyanosis .
Cyanoses .
A bluish or purplish discoloration of the skin and mucous membranes due to an increase in the amount of deoxygenated hemoglobin in the blood or a structural defect in the hemoglobin molecule. .
0.43
1413746