{
    "disease_id": "DOID:0080255",
    "recommended_name": {
        "id": "DOID:0080255",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080255",
        "name": "Meier-Gorlin syndrome 8",
        "description": "A Meier-Gorlin syndrome that has_material_basis_in compound heterozygous mutation in the MCM5 gene on chromosome 22q12."
    },
    "synonyms": [
        {
            "id": "MONDO:0033046",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033046",
            "name": "Meier-Gorlin syndrome 8",
            "description": ""
        },
        {
            "id": "MONDO:0033046",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033046",
            "name": "Meier-Gorlin syndrome 8",
            "description": ""
        },
        {
            "id": "MONDO:0033046",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033046",
            "name": "MGORS8",
            "description": ""
        },
        {
            "id": "MIM:617564",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617564",
            "name": "Meier-Gorlin syndrome 8",
            "description": "Meier-Gorlin syndrome 8"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080255"
    ],
    "unlinked_id_list": []
}