{
    "disease_id": "DOID:0070717",
    "recommended_name": {
        "id": "DOID:0070717",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070717",
        "name": "developmental delay with sleep apnea",
        "description": "An autosomal dominant intellectual developmental disorder characterized by hypotonia, global developmental delay, central and/or obstructive sleep apnea, and feeding difficulties that has_material_basis_in heterozygous mutation in the KCNK3 gene on chromosome 2p23."
    },
    "synonyms": [
        {
            "id": "DOID:0070717",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070717",
            "name": "DDSA",
            "description": ""
        },
        {
            "id": "MONDO:0980728",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0980728",
            "name": "developmental delay with sleep apnea",
            "description": ""
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070717"
    ],
    "unlinked_id_list": []
}