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C01. Bacterial Infections and Mycoses (group results)

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C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities: all > Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] > Genetic Diseases, Inborn [MESH:D030342] > Anemia, Hemolytic, Congenital [MESH:D000745] > Thalassemia [MESH:D013789] > beta-Thalassemia [MESH:D017086]

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458 items, grouped by C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities (view ungrouped items)

Beta Thalassemia, Dominant Inclusion Body Type [MESH:C565834] (1)   
MESH:C565834
 Beta Thalassemia, Dominant Inclusion Body Type
C565834
 
  
  
  

Delta-Beta Thalassemia [MESH:C562716] (1)   
MESH:C562716
 Delta-Beta Thalassemia
C562716
 
  
  
  

Thalassemia, Beta+, Silent Allele [MESH:C566065] (1)   
MESH:C566065
 Thalassemia, Beta+, Silent Allele
C566065
 
  
  
  

Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis [MESH:C564050] (1)   
MESH:C564050
 Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis
C564050
 
  
  
  

 (others) (454)   
MESH:C000188
 alachlor
C000188
 
  
  
  
MESH:C000515
 cremophor EL
C000515
 
  
  
  
MESH:C001335
 hexachlorobutadiene
C001335
 
  
  
  
MESH:C001803
 tempol
C001803
 
  
  
  
MESH:C002202
 4-oxoretinoic acid
C002202
 
  
  
  
MESH:C002741
 N-nitrosomorpholine
C002741
 
  
  
  
all 454 items...