| Disease #03707 (CVID7 (immunodeficiency, variable, common, type 7 (CVID-7)), OMIM:614699)
        
          | Official abbreviation | CVID7 |  
          | Name | immunodeficiency, variable, common, type 7 (CVID-7) |  
          | OMIM ID | 614699 |  
          | Human Phenotype Ontology Project (HPO) | HPO |  
          | Inheritance | Autosomal recessive |  
          | Individuals reported having this disease | - |  
          | Phenotype entries for this disease | - |  
          | Associated with 1 gene | CR2 |  
          | Associated tissues | - |  
          | Disease features | - |  
          | Remarks | - |  
          | Date created | 2014-09-25 23:29:40 +02:00 (CEST) |  
          | Date last edited | 2021-12-10 21:51:32 +01:00 (CET) |  |