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 .
C15.378.071.141.560 Hemoglobinuria, Paroxysmal .
C15.378.190 Bone Marrow Diseases .
C15.378.190.625 Myelodysplastic Syndromes .
C15.378.190.625.460 Hemoglobinuria, Paroxysmal .
C15.378.420 Hemoglobinopathies .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.365 Hemoglobinopathies .
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 .
D12.776.124.400.463.588 Hemoglobin, Sickle .
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 .
D12.776.422.316.762.426.588 Hemoglobin, Sickle .
E01 Diagnosis .
E01.370 Diagnostic Techniques and Procedures .
E01.370.225 Clinical Laboratory Techniques .
E01.370.225.625 Hematologic Tests .
E01.370.225.625.410 Hemoglobinometry .
E05 Investigative Techniques .
E05.200 Clinical Laboratory Techniques .
E05.200.625 Hematologic Tests .
E05.200.625.410 Hemoglobinometry .
 Synonyms & Historicals
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. .
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. .
Hemoglobinuria, Paroxysmal .
Marchiafava-Micheli Syndrome .
Paroxysmal Hemoglobinuria .
Paroxysmal Hemoglobinuria, Cold .
Paroxysmal Hemoglobinuria, Nocturnal .
Cold Paroxysmal Hemoglobinuria .
Hemoglobinuria, Cold Paroxysmal .
Hemoglobinuria, Nocturnal Paroxysmal .
Hemoglobinuria, Paroxysmal Cold .
Hemoglobinuria, Paroxysmal Nocturnal .
Marchiafava Micheli Syndrome .
Nocturnal Paroxysmal Hemoglobinuria .
Syndrome, Marchiafava-Micheli .
Paroxysmal Cold Hemoglobinuria .
Paroxysmal Nocturnal Hemoglobinuria .
Paroxymal Cold Hemoglobinuria .
Paroxymal Nocturnal Hemoglobinuria .
Marchiafava-Micheli Syndrome .
A condition characterized by the recurrence of HEMOGLOBINURIA caused by intravascular HEMOLYSIS. In cases occurring upon cold exposure (paroxysmal cold hemoglobinuria), usually after infections, there is a circulating antibody which is also a cold hemolysin. In cases occurring during or after sleep (paroxysmal nocturnal hemoglobinuria), the clonal hematopoietic stem cells exhibit a global deficiency of cell membrane proteins. .
Hemoglobin, Sickle .
Deoxygenated Sickle Hemoglobin .
Deoxyhemoglobin S .
Hemoglobin SS .
Hemoglobin, Deoxygenated Sickle .
SS, Hemoglobin .
Sickle Hemoglobin .
Sickle Hemoglobin, Deoxygenated .
Hemoglobin S .
An abnormal hemoglobin resulting from the substitution of valine for glutamic acid at position 6 of the beta chain of the globin moiety. The heterozygous state results in sickle cell trait, the homozygous in sickle cell anemia. .
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. .
Hemoglobinopathies .
Hemoglobinopathy .
A group of inherited disorders characterized by structural alterations within the hemoglobin molecule. .
Hemoglobinometry .
Hemoglobinometries .
Measurement of hemoglobin concentration in blood. .