{
    "disease_id": "DOID:0111094", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012565", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012565", 
            "name": "Fanconi anemia, complementation group N"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012565", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012565", 
            "name": "Fanconi anemia complementation group type N"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012565", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012565", 
            "name": "Fanconi Anemia, complementation group type N"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012565", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012565", 
            "name": "FANCN"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012565", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012565", 
            "name": "Fanconi anemia, complementation group N; FANCN"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012565", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012565", 
            "name": "Fanconi anemia caused by mutation in PALB2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012565", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012565", 
            "name": "PALB2 Fanconi anemia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111094", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111094", 
            "name": "FANCN"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111094", 
        "description": "A Fanconi anemia that has_material_basis_in compound heterozygous mutation in the PALB2 gene on chromosome 16p12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111094", 
        "name": "Fanconi anemia complementation group N"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/610832", 
            "id": "610832", 
            "database": "MIM"
        }
    ]
}