|   
  
    | Disease #06629 (GINGF5 (fibromatosis, gingival, type 5), OMIM:617626)
        
          | Official abbreviation | GINGF5 |  
          | Name | fibromatosis, gingival, type 5 |  
          | OMIM ID | 617626 |  
          | Human Phenotype Ontology Project (HPO) | HPO |  
          | Inheritance | Autosomal dominant |  
          | Individuals reported having this disease | 3 |  
          | Phenotype entries for this disease | 3 |  
          | Associated with 1 gene | REST |  
          | Associated tissues | - |  
          | Disease features | - |  
          | Remarks | - |  
          | Date created | 2021-12-10 23:20:41 +01:00 (CET) |  
          | Date last edited | 2023-01-05 14:47:46 +01:00 (CET) |  
 
 Individuals
 |  
 
    Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
    Use our APIs  to retrieve data.
 |