All
 C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 +
 C16.320 Genetic Diseases, Inborn D030342 +
 C16.320.070 Anemia, Hemolytic, Congenital D000745 +
 C16.320.070.095 Anemia, Dyserythropoietic, Congenital D000742 
 C16.320.070.100 Anemia, Hemolytic, Congenital Nonspherocytic D000746 
 C16.320.070.150 Anemia, Sickle Cell D000755 +
 C16.320.070.365 Elliptocytosis, Hereditary D004612 
 C16.320.070.480 Glucosephosphate Dehydrogenase Deficiency D005955 
 C16.320.070.490 Hemoglobin C Disease D006445 
 C16.320.070.785 Spherocytosis, Hereditary D013103 
 C16.320.070.875 Thalassemia D013789 +