serw-MX  [xml]  

 DeCS Categories

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. Anemia, Sickle Cell .
C15.378. Hemoglobin SC Disease .
C15.378. Thalassemia .
C15.378. delta-Thalassemia .
C15.378.071.196 Anemia, Hypochromic .
C15.378.420 Hemoglobinopathies .
C15.378.420.155 Anemia, Sickle Cell .
C15.378.420.155.440 Hemoglobin SC Disease .
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 .
C16.320.070.150 Anemia, Sickle Cell .
C16.320.070.150.440 Hemoglobin SC Disease .
C16.320.070.875 Thalassemia .
C16.320.070.875.575 delta-Thalassemia .
C16.320.365 Hemoglobinopathies .
C16.320.365.155 Anemia, Sickle Cell .
C16.320.365.155.440 Hemoglobin SC Disease .
C16.320.365.826 Thalassemia .
C16.320.365.826.575 delta-Thalassemia .
C23 Pathological Conditions, Signs and Symptoms .
C23.888 Signs and Symptoms .
C23.888.942 Urological Manifestations .
C23.888.942.750 Proteinuria .
C23.888.942.750.634 Hemoglobinuria .
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 .
D12.776.124.400.463.338 Hemoglobin C .
D12.776.124.400.463.510 Hemoglobin M .
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 .
D12.776.422.316.762.426.338 Hemoglobin C .
D12.776.422.316.762.426.510 Hemoglobin M .
 Synonyms & Historicals
Anemia, Hypochromic .
Anemias, Hypochromic .
Chloroses .
Hypochromic Anemia .
Hypochromic Anemias .
Chlorosis .
Anemia characterized by a decrease in the ratio of the weight of hemoglobin to the volume of the erythrocyte, i.e., the mean corpuscular hemoglobin concentration is less than normal. The individual cells contain less hemoglobin than they could have under optimal conditions. Hypochromic anemia may be caused by iron deficiency from a low iron intake, diminished iron absorption, or excessive iron loss. It can also be caused by infections or other diseases, therapeutic drugs, lead poisoning, and other conditions. (Stedman, 25th ed; from Miale, Laboratory Medicine: Hematology, 6th ed, p393) .
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 A .
Normal adult human hemoglobin. The globin moiety consists of two alpha and two beta chains. .
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. .
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. .
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. .
Hemoglobin C .
A commonly occurring abnormal hemoglobin in which lysine replaces a glutamic acid residue at the sixth position of the beta chains. It results in reduced plasticity of erythrocytes. .
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. .