{
    "disease_id": "DOID:0111082", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013566", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013566", 
            "name": "Fanconi Anemia, complementation Group 50"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013566", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013566", 
            "name": "Fanconi anemia caused by mutation in FANCL"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013566", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013566", 
            "name": "FANCL"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013566", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013566", 
            "name": "Fanconi anemia, complementation group L; FANCL"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013566", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013566", 
            "name": "Fanconi Anemia, complementation group type 50"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013566", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013566", 
            "name": "FANCL Fanconi anemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013566", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013566", 
            "name": "Fanconi anemia, complementation group L"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013566", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013566", 
            "name": "Fanconi anemia complementation group type L"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111082", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111082", 
            "name": "FANCL"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111082", 
        "description": "A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the PHF9 gene on chromosome 2p16.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111082", 
        "name": "Fanconi anemia complementation group L"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111082#disease-associations", 
            "id": "0111082", 
            "database": "Alliance of Genome Resources"
        }
    ]
}