{
    "disease_id": "DOID:0111844",
    "recommended_name": {
        "id": "DOID:0111844",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111844",
        "name": "X-linked intellectual developmental disorder 108",
        "description": "A syndromic X-linked intellectual disability characterized by global developmental delay, delayed walking, and poor speech acquisition that has_material_basis_in hemizygous mutation in the SLC9A7 gene on chromosome Xp11.3."
    },
    "synonyms": [
        {
            "id": "DOID:0111844",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111844",
            "name": "MRX108",
            "description": ""
        },
        {
            "id": "MONDO:0026723",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0026723",
            "name": "intellectual developmental disorder, X-linked 108",
            "description": ""
        },
        {
            "id": "MONDO:0026723",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0026723",
            "name": "intellectual developmental disorder, X-linked 108, X-linked recessive",
            "description": ""
        },
        {
            "id": "MONDO:0026723",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0026723",
            "name": "MRX108",
            "description": ""
        },
        {
            "id": "MIM:301024",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/301024",
            "name": "Intellectual developmental disorder, X-linked 108",
            "description": "Intellectual developmental disorder, X-linked 108"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111844"
    ],
    "unlinked_id_list": []
}