{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013499", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013499", 
            "name": "SLX4 Fanconi anemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013499", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013499", 
            "name": "Fanconi anemia complementation group type P"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013499", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013499", 
            "name": "Fanconi anemia, complementation group P; FANCP"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013499", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013499", 
            "name": "Fanconi anemia caused by mutation in Slx4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013499", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013499", 
            "name": "Fanconi anemia, complementation group P"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013499", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013499", 
            "name": "Fanconi Anemia, complementation group type P"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013499", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013499", 
            "name": "FANCP"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111092", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111092", 
            "name": "FANCP"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111092", 
        "description": "A Fanconi anemia characterized by increased chromosomal instability, progressive bone marrow failure and in some cases skeletal abnormalities that has_material_basis_in homozygous or compound heterozygous mutation in the SLX4 gene on chromosome 16p13.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111092", 
        "name": "Fanconi anemia complementation group P"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/613951", 
            "id": "613951", 
            "database": "MIM"
        }
    ]
}