{
    "disease_id": "DOID:0111083", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009214", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009214", 
            "name": "FAD2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009214", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009214", 
            "name": "Fanconi anemia, complementation group D2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009214", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009214", 
            "name": "FA4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009214", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009214", 
            "name": "Fanconi pancytopenia type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009214", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009214", 
            "name": "Fanconi pancytopenia, type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009214", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009214", 
            "name": "Fanconi Anemia, complementation group D"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009214", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009214", 
            "name": "Fanconi anemia, complementation group D2; FANCD2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009214", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009214", 
            "name": "FANCD2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111083", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111083", 
            "name": "FA4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111083", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111083", 
            "name": "FAD2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111083", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111083", 
            "name": "FANCD2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111083", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111083", 
            "name": "Fanconi pancytopenia type 4"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111083", 
        "description": "A Fanconi anemia that has_material_basis_in compound heterozygous or homozygous mutation in the FANCD2 gene on chromosome 3p25.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111083", 
        "name": "Fanconi anemia complementation group D2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111083#disease-associations", 
            "id": "0111083", 
            "database": "Alliance of Genome Resources"
        }
    ]
}