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    | Disease #05435 (DEE92;IECEE2 (encephalopathy, developmental and epileptic, type92 (IECEE2)), OMIM:617829)
        
          | Official abbreviation | DEE92;IECEE2 |  
          | Name | encephalopathy, developmental and epileptic, type92 (IECEE2) |  
          | OMIM ID | 617829 |  
          | Human Phenotype Ontology Project (HPO) | HPO |  
          | Inheritance | Autosomal dominant |  
          | Individuals reported having this disease | 1 |  
          | Phenotype entries for this disease | 1 |  
          | Associated with 1 gene | GABRB2 |  
          | Associated tissues | - |  
          | Disease features | autosomal dominant |  
          | Remarks | - |  
          | Date created | 2018-06-01 14:38:04 +02:00 (CEST) |  
          | Date last edited | 2023-10-23 12:25:49 +02:00 (CEST) |  
 
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