{
    "disease_id": "DOID:0111089", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011584", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011584", 
            "name": "Fanconi anemia, complementation group D1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011584", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011584", 
            "name": "FANCD1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011584", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011584", 
            "name": "inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011584", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011584", 
            "name": "Fanconi anemia, complementation group D1; FANCD1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011584", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011584", 
            "name": "Fad1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111089", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111089", 
            "name": "FAD1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111089", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111089", 
            "name": "FANCD1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111089", 
        "description": "A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the BRCA2 gene on chromosome 13q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111089", 
        "name": "Fanconi anemia complementation group D1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111089#disease-associations", 
            "id": "0111089", 
            "database": "Alliance of Genome Resources"
        }
    ]
}