{
    "disease_id": "DOID:0081224",
    "recommended_name": {
        "id": "DOID:0081224",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0081224",
        "name": "autosomal recessive intellectual developmental disorder 63",
        "description": "An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous mutation in the CAMK2A gene on chromosome 5q32."
    },
    "synonyms": [
        {
            "id": "MONDO:0054861",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054861",
            "name": "intellectual disability, autosomal recessive 63",
            "description": ""
        },
        {
            "id": "MONDO:0054861",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054861",
            "name": "intellectual disability, autosomal recessive 63",
            "description": ""
        },
        {
            "id": "MONDO:0054861",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054861",
            "name": "MRT63",
            "description": ""
        },
        {
            "id": "MONDO:0054861",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054861",
            "name": "mental retardation, autosomal recessive 63",
            "description": ""
        },
        {
            "id": "MIM:618095",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618095",
            "name": "Intellectual developmental disorder, autosomal recessive 63",
            "description": "Intellectual developmental disorder, autosomal recessive 63"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0081224"
    ],
    "unlinked_id_list": []
}