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 DeCS Categories

A11 Cells .
A11.118 Blood Cells .
A11.118.290 Erythrocytes .
A11.443 Erythroid Cells .
A11.443.240 Erythrocytes .
A15 Hemic and Immune Systems .
A15.145 Blood .
A15.145.229 Blood Cells .
A15.145.229.334 Erythrocytes .
C13 Female Urogenital Diseases and Pregnancy Complications .
C13.703 Pregnancy Complications .
C13.703.277 Fetal Diseases .
C13.703.277.060 Erythroblastosis, Fetal .
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 .
C15.378.071.141.150.480 Glucosephosphate Dehydrogenase Deficiency .
C15.378.295 Erythroblastosis, Fetal .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.300 Fetal Diseases .
C16.300.060 Erythroblastosis, Fetal .
C16.320 Genetic Diseases, Inborn .
C16.320.070 Anemia, Hemolytic, Congenital .
C16.320.070.480 Glucosephosphate Dehydrogenase Deficiency .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.202 Carbohydrate Metabolism, Inborn Errors .
C16.320.565.202.402 Glucosephosphate Dehydrogenase Deficiency .
C16.614 Infant, Newborn, Diseases .
C16.614.304 Erythroblastosis, Fetal .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.202 Carbohydrate Metabolism, Inborn Errors .
C18.452.648.202.402 Glucosephosphate Dehydrogenase Deficiency .
C20 Immune System Diseases .
C20.306 Erythroblastosis, Fetal .
G09 Circulatory and Respiratory Physiological Phenomena .
G09.188 Blood Physiological Phenomena .
G09.188.370 Hemorheology .
G09.188.370.249 Erythrocyte Deformability .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Anemia, Hemolytic, Congenital .
Congenital Hemolytic Anemia .
Hemolytic Anemia, Congenital .
Hemolytic Anemia, Hereditary .
Hereditary Hemolytic Anemia .
Anemia, Congenital Hemolytic .
Anemia, Hereditary Hemolytic .
Anemias, Congenital Hemolytic .
Anemias, Hereditary Hemolytic .
Congenital Hemolytic Anemias .
Hemolytic Anemias, Congenital .
Hemolytic Anemias, Hereditary .
Hereditary Hemolytic Anemias .
Anemia, Hemolytic, Hereditary .
Hemolytic anemia due to various intrinsic defects of the erythrocyte. .
1.00
491586
 
Glucosephosphate Dehydrogenase Deficiency .
Deficiency of Glucose-6-Phosphate Dehydrogenase .
Deficiency, GPD .
Deficiency, Glucosephosphate Dehydrogenase .
G6PD Deficiency .
GPD Deficiency .
Glucose 6 Phosphate Dehydrogenase Deficiency .
Glucose-6-Phosphate Dehydrogenase Deficiency .
Glucosephosphate Dehydrogenase Deficiencies .
Hemolytic Anemia Due to G6PD Deficiency .
Deficiencies, G6PD .
Deficiencies, GPD .
Deficiencies, Glucose-6-Phosphate Dehydrogenase .
Deficiencies, Glucosephosphate Dehydrogenase .
Deficiency of Glucose 6 Phosphate Dehydrogenase .
Deficiency, G6PD .
Deficiency, Glucose-6-Phosphate Dehydrogenase .
Dehydrogenase Deficiencies, Glucose-6-Phosphate .
Dehydrogenase Deficiencies, Glucosephosphate .
Dehydrogenase Deficiency, Glucose-6-Phosphate .
Dehydrogenase Deficiency, Glucosephosphate .
G6PD Deficiencies .
GPD Deficiencies .
Glucose-6-Phosphate Dehydrogenase Deficiencies .
A disease-producing enzyme deficiency subject to many variants, some of which cause a deficiency of GLUCOSE-6-PHOSPHATE DEHYDROGENASE activity in erythrocytes, leading to hemolytic anemia. .
0.51
764001
 
Anemia, Hemolytic .
Hemolytic Anemia, Acquired .
Microangiopathic Hemolytic Anemia .
Acquired Hemolytic Anemia .
Anemia, Acquired Hemolytic .
Microangiopathic Anemia .
Anemia, Hemolytic, Acquired .
Anemia, Microangiopathic .
Hemolytic Anemia .
A condition of inadequate circulating red blood cells (ANEMIA) or insufficient HEMOGLOBIN due to premature destruction of red blood cells (ERYTHROCYTES). .
0.47
2358467
 
Erythrocytes .
Red Blood Corpuscles .
Blood Cell, Red .
Blood Corpuscle, Red .
Corpuscle, Red Blood .
Corpuscles, Red Blood .
Erythrocyte .
Red Blood Cell .
Red Blood Corpuscle .
Blood Corpuscles, Red .
Blood Cells, Red .
Red Blood Cells .
Red blood cells. Mature erythrocytes are non-nucleated, biconcave disks containing HEMOGLOBIN whose function is to transport OXYGEN. .
0.43
671115338
 
Erythroblastosis, Fetal .
Erythroblastosis Fetalis .
Erythroblastoses, Fetal .
Erythroblastosis Fetali .
Fetal Erythroblastoses .
Fetal Erythroblastosis .
Fetali, Erythroblastosis .
Fetalis, Erythroblastosis .
Newborn Hemolytic Disease .
Newborn Hemolytic Diseases .
Hemolytic Disease of Newborn .
A condition characterized by the abnormal presence of ERYTHROBLASTS in the circulation of the FETUS or NEWBORNS. It is a disorder due to BLOOD GROUP INCOMPATIBILITY, such as the maternal alloimmunization by fetal antigen RH FACTORS leading to HEMOLYSIS of ERYTHROCYTES, hemolytic anemia (ANEMIA, HEMOLYTIC), general edema (HYDROPS FETALIS), and SEVERE JAUNDICE IN NEWBORN. .
0.43
1835542
 
Erythrocyte Deformability .
Deformability, Erythrocyte .
Filterability, Erythrocyte .
Erythrocyte Filterability .
Ability of ERYTHROCYTES to change shape as they pass through narrow spaces, such as the microvasculature. .
0.39
103210