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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] > Metabolism, Inborn Errors [MESH:D008661] > Brain Diseases, Metabolic, Inborn [MESH:D020739] > Lysosomal Storage Diseases, Nervous System [MESH:D020140] > Sphingolipidoses [MESH:D013106] > Gangliosidoses [MESH:D005733] > Gangliosidoses, GM2 [MESH:D020143] > Sandhoff Disease [MESH:D012497]

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

Sandhoff Disease, Adult Type [MESH:C564825] (1)   
MESH:C564825
 Sandhoff Disease, Adult Type
C564825
 
  
  
  

Sandhoff Disease, Infantile Type [MESH:C564827] (1)   
MESH:C564827
 Sandhoff Disease, Infantile Type
C564827
 
  
  
  

Sandhoff Disease, Juvenile Type [MESH:C564826] (1)   
MESH:C564826
 Sandhoff Disease, Juvenile Type
C564826
 
  
  
  

 (others) (70)   
MESH:C004369
 2-phenylphenol
C004369
 
  
  
  
MESH:C006253
 pirinixic acid
C006253
 
  
  
  
MESH:C008261
 lead acetate
C008261
 
  
  
  
MESH:C010327
 salinomycin
C010327
 
  
  
  
MESH:C012568
 terbufos
C012568
 
  
  
  
MESH:C015408
 oxatomide
C015408
 
  
  
  
all 70 items...