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 DeCS Categories

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, Hemolytic, Congenital Nonspherocytic .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.070 Anemia, Hemolytic, Congenital .
C16.320.070.100 Anemia, Hemolytic, Congenital Nonspherocytic .
 Synonyms & Historicals
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. .
Anemia, Hemolytic, Congenital Nonspherocytic .
Anemia, Congenital Nonspherocytic Hemolytic .
Anemia, Hemolytic Congenital, Nonspherocytic .
Congenital Nonspherocytic Hemolytic Anemia .
Hemolytic Anemia, Congenital Nonspherocytic .
Any one of a group of congenital hemolytic anemias in which there is no abnormal hemoglobin or spherocytosis and in which there is a defect of glycolysis in the erythrocyte. Common causes include deficiencies in GLUCOSE-6-PHOSPHATE ISOMERASE; PYRUVATE KINASE; and GLUCOSE-6-PHOSPHATE DEHYDROGENASE. .
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). .