{
    "disease_id": "DOID:0112031",
    "recommended_name": {
        "id": "DOID:0112031",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0112031",
        "name": "non-syndromic X-linked intellectual disability 89",
        "description": "A non-syndromic X-linked intellectual disability characterized by severe developmental delay that has_material_basis_in heterozygous mutation in a region on chromosome Xp11.3."
    },
    "synonyms": [
        {
            "id": "DOID:0112031",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112031",
            "name": "MRX89",
            "description": ""
        },
        {
            "id": "DOID:0112031",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112031",
            "name": "X-linked mental retardation 89",
            "description": ""
        },
        {
            "id": "MONDO:0010450",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010450",
            "name": "MRX89",
            "description": ""
        },
        {
            "id": "MONDO:0010450",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010450",
            "name": "MRX89",
            "description": ""
        },
        {
            "id": "MONDO:0010450",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010450",
            "name": "mental retardation, X-linked 89",
            "description": ""
        },
        {
            "id": "MONDO:0010450",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010450",
            "name": "mental retardation, X-linked 89; MRX89",
            "description": ""
        }
    ]
}