{
    "disease_id": "DOID:0060947",
    "recommended_name": {
        "id": "DOID:0060947",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060947",
        "name": "autosomal recessive intellectual developmental disorder 82",
        "description": "An autosomal recessive intellectual developmental disorder characterized by global developmental delay with motor and speech delay, variably impaired intellectual development, and behavioral abnormalities has_material_basis_in homozygous mutation in the NSUN6 gene on chromosome 10p12."
    },
    "synonyms": [
        {
            "id": "MONDO:0968944",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0968944",
            "name": "intellectual developmental disorder, autosomal recessive 82",
            "description": ""
        },
        {
            "id": "MIM:620779",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620779",
            "name": "Intellectual developmental disorder, autosomal recessive 82",
            "description": "Intellectual developmental disorder, autosomal recessive 82"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060947"
    ],
    "unlinked_id_list": []
}