[ON THE DIFFERENTIAL DIAGNOSIS OF HEREDITARY NON-SPHEROCYTIC HEMOLYTIC ANEMIAS].
D000740:Anemia; D000743:Anemia, Hemolytic; D000745:Anemia, Hemolytic, Congenital; D000746:Anemia, Hemolytic, Congenital Nonspherocytic; D017487:Ankyrins / Q000172:deficiency; D002648:Child; D003937:Diagnosis, Differential; D005826:Genetics, Medical; D005955:Glucosephosphate Dehydrogenase Deficiency; D005958:Glucosephosphates; D005978:Glutathione; D006801:Humans; D007223:Infant; D041781:Jaundice, Obstructive; D008659:Metabolic Diseases; D010088:Oxidoreductases; D010733:Phosphoglucomutase; D010770:Phosphotransferases; D013103:Spherocytosis, Hereditary
D017487:Ankyrins; D005958:Glucosephosphates; D010088:Oxidoreductases; D010770:Phosphotransferases; D010733:Phosphoglucomutase; D005978:Glutathione
ANEMIA, HEMOLYTIC; ANEMIA, HEMOLYTIC, CONGENITAL NONSPHEROCYTIC; CHILD; DIAGNOSIS, DIFFERENTIAL; GENETICS, HUMAN; GLUCOSEPHOSPHATE DEHY- DROGENASE DEFICIENCY; GLUTATHIONE; INFANT; METABOLIC DISEASES; OXIDOREDUCTASES; PHOSPHOGLUCOMUTASE; PHOSPHOTRANSFERASES
ZUR DIFFERENTIALDIAGNOSE DER HEREDITAEREN NICHTSPHAEROZYTAEREN HAEMOLYTISCHEN ANAEMIEN.