{
    "disease_id": "DOID:0051010",
    "recommended_name": {
        "id": "DOID:0051010",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0051010",
        "name": "Bryant-Li-Bhoj neurodevelopmental syndrome",
        "description": "An autosomal dominant intellectual developmental disorder that is characterized by developmental delay / intellectual disability (typically in the severe range) and nonspecific craniofacial abnormalities."
    },
    "synonyms": [
        {
            "id": "MONDO:0030606",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030606",
            "name": "Bryant-Li-Bhoj neurodevelopmental syndrome 1",
            "description": ""
        },
        {
            "id": "MONDO:0030606",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030606",
            "name": "BRYLIB1",
            "description": ""
        },
        {
            "id": "MIM:619720",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619720",
            "name": "Bryant-Li-Bhoj neurodevelopmental syndrome 1",
            "description": "Bryant-Li-Bhoj neurodevelopmental syndrome 1"
        }
    ],
    "children": [
        {
            "id": "DOID:0051011",
            "label": "Bryant-Li-Bhoj neurodevelopmental syndrome 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0051012",
            "label": "Bryant-Li-Bhoj neurodevelopmental syndrome 2",
            "link_status": true,
            "children": []
        }
    ],
    "id_list": [
        "DOID:0051010",
        "DOID:0051011",
        "DOID:0051012"
    ],
    "unlinked_id_list": []
}