{
    "disease_id": "DOID:0070043",
    "recommended_name": {
        "id": "DOID:0070043",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070043",
        "name": "autosomal dominant intellectual developmental disorder 13",
        "description": "An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the DYNC1H1 gene on chromosome 14q32.31."
    },
    "synonyms": [
        {
            "id": "DOID:0070043",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070043",
            "name": "MRD13",
            "description": ""
        },
        {
            "id": "DOID:0070043",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070043",
            "name": "autosomal dominant mental retardation 13",
            "description": ""
        },
        {
            "id": "DOID:0070043",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070043",
            "name": "mental retardation, autosomal dominant 13, with neuronal migration defects",
            "description": ""
        },
        {
            "id": "DOID:0070043",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070043",
            "name": "autosomal dominant non-syndromic intellectual disability 13",
            "description": ""
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070043"
    ],
    "unlinked_id_list": []
}