| Disease #03092 (EDAID2 (dysplasia, ectodermal, and immunodeficiency, type 2 (EDAID-2)), OMIM:612132)
        
          | Official abbreviation | EDAID2 |  
          | Name | dysplasia, ectodermal, and immunodeficiency, type 2 (EDAID-2) |  
          | OMIM ID | 612132 |  
          | Human Phenotype Ontology Project (HPO) | HPO |  
          | Inheritance | Autosomal dominant |  
          | Individuals reported having this disease | - |  
          | Phenotype entries for this disease | - |  
          | Associated with 1 gene | NFKBIA |  
          | Associated tissues | - |  
          | Disease features | autosomal dominant |  
          | Remarks | - |  
          | Date created | 2014-09-25 23:29:40 +02:00 (CEST) |  
          | Date last edited | 2021-12-10 21:51:32 +01:00 (CET) |  |