Disease #05747 (OPTB (osteopetrosis, autosomal recessive (OPTB)))
      
        
          | Official abbreviation | 
          OPTB |  
        
          | Name | 
          osteopetrosis, autosomal recessive (OPTB) |  
        
          | OMIM ID | 
          - |  
        
          | Inheritance | 
          Autosomal dominant |  
        
          | Individuals reported having this disease | 
          10 |  
        
          | Phenotype entries for this disease | 
          10 |  
        
          | Associated with 0 genes | 
          - |  
        
          | Associated tissues | 
          - |  
        
          | Disease features | 
          - |  
        
          | Remarks | 
          - |  
        
          | Date created | 
          2020-05-18 09:28:28 +02:00 (CEST) |  
        
          | Date last edited | 
          2021-12-10 21:51:32 +01:00 (CET) |   
  
      Individuals
      
      
       
      
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