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    | Disease #05854 (NS2 (Noonan syndrome, type 2 (NS2)), OMIM:605275)
        
          | Official abbreviation | NS2 |  
          | Name | Noonan syndrome, type 2 (NS2) |  
          | OMIM ID | 605275 |  
          | Human Phenotype Ontology Project (HPO) | HPO |  
          | Inheritance | Autosomal recessive |  
          | Individuals reported having this disease | 1 |  
          | Phenotype entries for this disease | 1 |  
          | Associated with 1 gene | LZTR1 |  
          | Associated tissues | - |  
          | Disease features | - |  
          | Remarks | - |  
          | Date created | 2020-10-16 09:46:56 +02:00 (CEST) |  
          | Date last edited | 2021-12-10 21:51:32 +01:00 (CET) |  
 
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