{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014986", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014986", 
            "name": "Fanconi anemia complementation group type R"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014986", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014986", 
            "name": "RAD51 Fanconi anemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014986", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014986", 
            "name": "Fanconi Anemia, complementation group R"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014986", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014986", 
            "name": "Fanconi anemia caused by mutation in RAD51"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014986", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014986", 
            "name": "Fanconi Anemia, complementation group type R"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014986", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014986", 
            "name": "Fanconi anemia, complementation GROUP R; FANCR"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014986", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014986", 
            "name": "FANCR"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111090", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111090", 
            "name": "FANCR"
        }, 
        {
            "url": "https://www.omim.org/entry/617244", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:617244", 
            "name": "Fanconi anemia, complementation group R"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111090", 
        "description": "A Fanconi anemia that has_material_basis_in heterozygous mutation in the RAD51 gene on chromosome 15q15.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111090", 
        "name": "Fanconi anemia complementation group R"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/617244", 
            "id": "617244", 
            "database": "MIM"
        }
    ]
}