{
    "disease_id": "DOID:0112054",
    "recommended_name": {
        "id": "DOID:0112054",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0112054",
        "name": "non-syndromic X-linked intellectual disability 107",
        "description": "A non-syndromic X-linked intellectual disability characterized by mild to moderate intellectual disability that has_material_basis_in heterozygous or hemizygous mutation in CXorf56 on chromosome Xq24."
    },
    "synonyms": [
        {
            "id": "DOID:0112054",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112054",
            "name": "MRX107",
            "description": ""
        },
        {
            "id": "DOID:0112054",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112054",
            "name": "X-linked mental retardation 107",
            "description": ""
        },
        {
            "id": "MONDO:0049222",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0049222",
            "name": "intellectual disability, x-linked 107",
            "description": ""
        },
        {
            "id": "MONDO:0049222",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0049222",
            "name": "mental retardation, X-linked 107; MRX107",
            "description": ""
        },
        {
            "id": "MONDO:0049222",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0049222",
            "name": "MRX107",
            "description": ""
        },
        {
            "id": "MIM:301013",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/301013",
            "name": "Intellectual developmental disorder, X-linked 107",
            "description": "Intellectual developmental disorder, X-linked 107"
        }
    ]
}