Disease #00093 (WARBM3 (Warburg micro syndrome, type 3 (WARBM3)), OMIM:614222)
      
        
          | Official abbreviation | 
          WARBM3 |  
        
          | Name | 
          Warburg micro syndrome, type 3 (WARBM3) |  
        
          | OMIM ID | 
          614222 |  
        
          | Human Phenotype Ontology Project (HPO) | 
          HPO |  
        
          | Inheritance | 
          Autosomal recessive |  
        
          | Individuals reported having this disease | 
          - |  
        
          | Phenotype entries for this disease | 
          2 |  
        
          | Associated with 1 gene | 
          RAB18 |  
        
          | Associated tissues | 
          - |  
        
          | Disease features | 
          - |  
        
          | Remarks | 
          - |  
        
          | Date created | 
          2012-12-10 09:11:24 +01:00 (CET) |  
        
          | Date last edited | 
          2021-12-10 21:51:32 +01:00 (CET) |   
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