{
    "disease_id": "DOID:0061126",
    "recommended_name": {
        "id": "DOID:0061126",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0061126",
        "name": "Brunet-Wagner neurodevelopmental syndrome",
        "description": "An autosomal recessive intellectual developmental disorder characterized by infantile hypotonia and severely impaired development affecting both motor and cognitive skills that has_material_basis_in homozygous or compound heterozygous mutation in the RBL2 gene on chromosome 16q12."
    },
    "synonyms": [
        {
            "id": "DOID:0061126",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0061126",
            "name": "BRUWAG",
            "description": ""
        },
        {
            "id": "MONDO:0859217",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0859217",
            "name": "Brunet-Wagner neurodevelopmental syndrome",
            "description": ""
        },
        {
            "id": "MIM:619690",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619690",
            "name": "Brunet-Wagner neurodevelopmental syndrome",
            "description": "Brunet-Wagner neurodevelopmental syndrome"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061126"
    ],
    "unlinked_id_list": []
}