| Disease #00012
        
          | Official abbreviation | FANCD1 |  
          | Name | Fanconi anemia, complementation group D1 |  
          | OMIM ID | 605724 |  
          | Human Phenotype Ontology Project (HPO) | HPO |  
          | Inheritance | - |  
          | Individuals reported having this disease | 0 |  
          | Phenotype entries for this disease | 0 |  
          | Associated with 1 gene | BRCA2 |  
          | Associated tissues | - |  
          | Disease features | - |  
          | Remarks | - |  |