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 .
C12 Male Urogenital Diseases .
C12.777 Urologic Diseases .
C12.777.934 Urination Disorders .
C12.777.934.734 Proteinuria .
C12.777.934.734.634 Hemoglobinuria .
C13 Female Urogenital Diseases and Pregnancy Complications .
C13.351 Female Urogenital Diseases .
C13.351.968 Urologic Diseases .
C13.351.968.934 Urination Disorders .
C13.351.968.934.734 Proteinuria .
C13.351.968.934.734.634 Hemoglobinuria .
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. delta-Thalassemia .
C15.378.420 Hemoglobinopathies .
C15.378.420.826 Thalassemia .
C15.378.420.826.200 delta-Thalassemia .
C15.378.619 Methemoglobinemia .
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 .
C23.888.942 Urological Manifestations .
C23.888.942.750 Proteinuria .
C23.888.942.750.634 Hemoglobinuria .
D09 Carbohydrates .
D09.400 Glycoconjugates .
D09.400.430 Glycoproteins .
D09.400.430.937 Glycated Hemoglobin A .
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 .
D12.776.124.400.405.440 Glycated Hemoglobin A .
D12.776.124.400.463 Hemoglobins, Abnormal .
D12.776.124.400.463.510 Hemoglobin M .
D12.776.395 Glycoproteins .
D12.776.395.381 Glycated Hemoglobin A .
D12.776.422 Hemeproteins .
D12.776.422.316 Globins .
D12.776.422.316.762 Hemoglobins .
D12.776.422.316.762.380 Hemoglobin A .
D12.776.422.316.762.380.440 Glycated Hemoglobin A .
D12.776.422.316.762.426 Hemoglobins, Abnormal .
D12.776.422.316.762.426.510 Hemoglobin M .
 Synonyms & Historicals
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. .
Methemoglobinemia .
Methemoglobinemias .
The presence of methemoglobin in the blood, resulting in cyanosis. A small amount of methemoglobin is present in the blood normally, but injury or toxic agents convert a larger proportion of hemoglobin into methemoglobin, which does not function reversibly as an oxygen carrier. Methemoglobinemia may be due to a defect in the enzyme NADH methemoglobin reductase (an autosomal recessive trait) or to an abnormality in hemoglobin M (an autosomal dominant trait). (Dorland, 27th ed) .
Hemoglobin A .
Normal adult human hemoglobin. The globin moiety consists of two alpha and two beta chains. .
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. .
Hemoglobin M .
A group of abnormal hemoglobins in which amino acid substitutions take place in either the alpha or beta chains but near the heme iron. This results in facilitated oxidation of the hemoglobin to yield excess methemoglobin which leads to cyanosis. .
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. .
Hemoglobinuria .
The presence of free HEMOGLOBIN in the URINE, indicating hemolysis of ERYTHROCYTES within the vascular system. After saturating the hemoglobin-binding proteins (HAPTOGLOBINS), free hemoglobin begins to appear in the urine. .
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. .
Glycated Hemoglobin A .
Glycated Hemoglobin A1c .
Glycated Hemoglobins .
Glycosylated Hemoglobin A1c .
Hb A1 .
Hb A1a+b .
Hb A1a-1 .
Hb A1a-2 .
Hb A1b .
Hemoglobin, Glycated A1a-2 .
Hemoglobin, Glycated A1b .
Hemoglobin, Glycosylated .
Hemoglobin, Glycosylated A1a-1 .
Hemoglobin, Glycosylated A1b .
A1a-1 Hemoglobin, Glycosylated .
A1a-2 Hemoglobin, Glycated .
A1b Hemoglobin, Glycated .
A1b Hemoglobin, Glycosylated .
Glycated A1a-2 Hemoglobin .
Glycated A1b Hemoglobin .
Glycosylated A1a-1 Hemoglobin .
Glycosylated A1b Hemoglobin .
Glycosylated Hemoglobin .
Hemoglobin A, Glycated .
Hemoglobin A1c, Glycated .
Hemoglobin A1c, Glycosylated .
Hemoglobin, Glycated A1a 2 .
Hemoglobin, Glycosylated A1a 1 .
Hemoglobins, Glycated .
Glycohemoglobin A .
Glycosylated Hemoglobin A .
Hb A1c .
HbA1 12269 .
Hemoglobin A(1) .
Hemoglobin A, Glycosylated .
Products of non-enzymatic reactions between GLUCOSE and HEMOGLOBIN A, occurring as a minor fraction of the hemoglobin components of human erythrocytes. Hemoglobin A1c is hemoglobin A with glucose covalently bound to the terminal VALINE of the beta chain. Glycated hemoglobin A is used as an index of the average blood sugar level over a lifetime of erythrocytes. .