{
    "disease_id": "DOID:0111092",
    "recommended_name": {
        "id": "DOID:0111092",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111092",
        "name": "Fanconi anemia complementation group P",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0111092",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111092",
            "name": "FANCP",
            "description": ""
        },
        {
            "id": "MONDO:0013499",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013499",
            "name": "Fanconi anemia complementation group P",
            "description": "Any Fanconi anemia in which the cause of the disease is a mutation in the SLX4 gene."
        },
        {
            "id": "MONDO:0013499",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013499",
            "name": "FANCP",
            "description": ""
        },
        {
            "id": "MONDO:0013499",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013499",
            "name": "Fanconi Anemia, complementation group type P",
            "description": ""
        },
        {
            "id": "MONDO:0013499",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013499",
            "name": "Fanconi anaemia caused by mutation in SLX4",
            "description": ""
        },
        {
            "id": "MONDO:0013499",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013499",
            "name": "Fanconi anaemia caused by mutation in Slx4",
            "description": ""
        },
        {
            "id": "MONDO:0013499",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013499",
            "name": "Fanconi anaemia complementation group type P",
            "description": ""
        },
        {
            "id": "MONDO:0013499",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013499",
            "name": "Fanconi anemia caused by mutation in SLX4",
            "description": ""
        },
        {
            "id": "MONDO:0013499",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013499",
            "name": "Fanconi anemia caused by mutation in Slx4",
            "description": ""
        },
        {
            "id": "MONDO:0013499",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013499",
            "name": "Fanconi anemia complementation group type P",
            "description": ""
        },
        {
            "id": "MONDO:0013499",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013499",
            "name": "SLX4 Fanconi anaemia",
            "description": ""
        },
        {
            "id": "MONDO:0013499",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013499",
            "name": "SLX4 Fanconi anemia",
            "description": ""
        },
        {
            "id": "MONDO:0013499",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013499",
            "name": "Slx4 Fanconi anaemia",
            "description": ""
        },
        {
            "id": "MONDO:0013499",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013499",
            "name": "Slx4 Fanconi anemia",
            "description": ""
        },
        {
            "id": "MONDO:0013499",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013499",
            "name": "Fanconi anemia, complementation group P",
            "description": ""
        },
        {
            "id": "MIM:613951",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613951",
            "name": "Fanconi anemia complementation group P",
            "description": "Fanconi anemia complementation group P"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111092"
    ],
    "unlinked_id_list": []
}