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    | Disease #01483 (OPTA2 (osteopetrosis, autosomal dominant, type 2), OMIM:166600)
        
          | Official abbreviation | OPTA2 |  
          | Name | osteopetrosis, autosomal dominant, type 2 |  
          | OMIM ID | 166600 |  
          | 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 | CLCN7 |  
          | Associated tissues | - |  
          | Disease features | - |  
          | Remarks | - |  
          | Date created | 2014-09-25 23:29:40 +02:00 (CEST) |  
          | Date last edited | 2025-05-05 09:47:20 +02:00 (CEST) |  
 
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