{
    "disease_id": "DOID:0060929",
    "recommended_name": {
        "id": "DOID:0060929",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060929",
        "name": "non-syndromic X-linked intellectual developmental disorder 111",
        "description": "A non-syndromic X-linked intellectual disability characterized by different degrees of impaired intellectual development associated with motor, speech and behavioral impairments that has_material_basis_in hemizygous or heterozygous mutation in the SLITRK2 gene on chromosome Xq27."
    },
    "synonyms": [
        {
            "id": "DOID:0060929",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060929",
            "name": "XLID111",
            "description": ""
        },
        {
            "id": "MONDO:0957203",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0957203",
            "name": "intellectual developmental disorder, X-linked 111",
            "description": ""
        },
        {
            "id": "MIM:301107",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/301107",
            "name": "Intellectual developmental disorder, X-linked 111",
            "description": "Intellectual developmental disorder, X-linked 111"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060929"
    ],
    "unlinked_id_list": []
}