|   
  
    | Phenotype #0000000914
        
          | Individual ID | 00001760 |  
          | Associated disease | SBCADD |  
          | Inheritance | Familial |  
          | Diagnosis/Initial | - |  
          | Age/Examination | - |  
          | Diagnosis/Definite | - |  
          | Age/Onset | 00y05m |  
          | Phenotype/Onset | - |  
          | Phenotype details | clinical presentation; seizures (which stopped), speech development was significantly delayed, mental retardation |  
          | Protein | - |  
          | Age/Diagnosis | 04y |  
          | Owner name | Division of Human Genetics, Innsbruck |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | Division of Human Genetics, Innsbruck |  
          | Date created | 2013-04-05 11:51:07 +02:00 (CEST) |  
          | Date last edited | 2013-05-13 09:38:49 +02:00 (CEST) |  |  
 
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